CN108318695A

CN108318695A - People RBP colloidal gold immunochromatographimethod quantitative testing test paper cards and its clinical application

Info

Publication number: CN108318695A
Application number: CN201810087161.7A
Authority: CN
Inventors: 马永; 丁娜
Original assignee: ZONHON BIOPHARMA INSTITUTE Inc; Jiangsu Jinghong Biological Medicine Technology Co Ltd
Current assignee: ZONHON BIOPHARMA INSTITUTE Inc; Jiangsu Jinghong Biological Medicine Technology Co Ltd
Priority date: 2018-01-30
Filing date: 2018-01-30
Publication date: 2018-07-24
Anticipated expiration: 2038-01-30
Also published as: CN108318695B

Abstract

The present invention relates to human retinol-binding protein colloidal gold immunochromatographimethod quantitative testing test paper card and its clinical applications.The present invention is prepared for a variety of human retinol-binding protein antibody, and carries out pairing screening, is finally obtained the antibody combination (B08 and B14) of sensitivity and specificity energy meet demand；It facilitates mass production simultaneously, can meet the needs of larger scale clinical application in the future.The debugging Optimization Work of system is detected to above-mentioned antibody combination, it obtains easy to operate, sensitivity, specificity and coherent detection performance can meet the colloidal gold quantitative test card of the human retinol-binding protein of people's clinical sample detection, and can meet the clinical detection of human blood or urine specimen.

Description

People RBP colloidal gold immunochromatographimethod quantitative testing test paper cards and its clinical application

Technical field

The invention belongs to biotechnologies, are specifically related to two kinds of anti-human RBP ELISA (Retinol- Binding Protein, RBP) antibody and preparation method thereof and above-mentioned antibody is in human retinol-binding protein colloid gold immune Application in the quantitative detection of chromatography.

Background technology

RBP ELISA (Retinol-Binding Protein, RBP) is by a polypeptide chain and fraction carbon aquation Close object composition, molecular weight about 21KD, 3~12 hours half-life period.RBP is mainly synthesized by liver, is regarded with being transported from liver cell Flavol is distributed widely in the function of surrounding tissue in blood, cerebrospinal fluid, urine and other body fluid.In blood, RBP with regard Flavol, prealbumin are with 1:1:The composite form of 1 (mol) exists, and 90% retinol is to body tissue in transporter.When When RBP is combined with the RBP receptors of cell surface, retinol enters into the cell, and compound disintegrates, and free RBP is filtered from glomerulus Go out, wherein the overwhelming majority is by proximal renal tubular epithelial cells reabsorption and is decomposed, utilizes for tissue, only arranged from urine on a small quantity Go out.The diseases such as internal zinc, asiderosis and severe infections can reduce the biosynthesis of RBP.

In protein malnutrition, the protein synthesis of liver is insufficient and causes RBP insufficient, and retinol cannot enter blood Liquid, retinol play regulatory role the secretion of RBP, and the two is proportionate.RBP participates in turning for vitamin A together with prealbumin Fortune, serum RBP and Serum Vitamin content have high correlation, therefore, it is considered that RBP can be used as the quick of reflection vitamin A deficiency Feel index.Separately some researches show that serum RBP levels are to reflect sensitive, the specific index of nutritive disease curative effect.It measures and regards Huang The functional lesion of alcohol binding protein energy early detection renal tubule, and can sensitively reflect the extent of damage of kidney proximal tubule, may be used also Index as liver function Random early Detection and monitoring and therapeutic.In clinic, serum RBP, which is quantitatively detected, can be used for each section office, such as nephrosis Section, ICU, emergency department, division of endocrinology, Gastroenterology dept., Department of Aged, paediatrics etc..

To sum up, it prepares anti-human RBP ELISA specific antibody and is quantified applied to human retinol-binding protein is prepared Detection kit has important clinical value.

Invention content

It can be effective, specific binding human retinol-binding protein the technical problem to be solved in the present invention is to provide one group Antibody.More specifically：

The first object of the present invention is to provide two kinds of anti-human RBP ELISA antibody.

The first anti-human RBP ELISA antibody (B08),

Its heavy chain variable region contains complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：Shown in 1 HCDR1, such as sequence SEQ ID NO：HCDR2 shown in 2, and/or such as sequence SEQ ID NO：HCDR3 shown in 3；

And its light-chain variable sequence contains complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：4 Shown in LCDR1, such as sequence SEQ ID NO：LCDR2 shown in 5, and/or such as sequence SEQ ID NO：LCDR3 shown in 6.

The amino acid of the first anti-human RBP ELISA antibody (B08) heavy chain variable region preferably in the present invention Sequence such as SEQ ID NO:Shown in 7；The amino acid sequence of light chain variable region such as SEQ ID NO:Shown in 8.

Second of anti-human RBP ELISA antibody (B14),

Its heavy chain variable region contains complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：Shown in 9 HCDR1, such as sequence SEQ ID NO：HCDR2 shown in 10, and/or such as sequence SEQ ID NO：HCDR3 shown in 11；

And its light-chain variable sequence contains complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：12 Shown in LCDR1, such as sequence SEQ ID NO：LCDR2 shown in 13, and/or such as sequence SEQ ID NO：LCDR3 shown in 14.

The amino acid of second of anti-human RBP ELISA antibody (B14) heavy chain variable region preferably in the present invention Sequence such as SEQ ID NO:Shown in 15；The amino acid sequence of light chain variable region such as SEQ ID NO:Shown in 16.

Second purpose of the invention is to provide two kinds of single-chain antibodies, is the amino acid sequence such as SEQ of single-chain antibody B08 respectively ID NO:Shown in 33, such as sequence SEQ ID NO after nucleotide sequence is optimized：Shown in 35；The amino acid sequence of single-chain antibody B14 Row such as SEQ ID NO:Shown in 34, such as sequence SEQ ID NO after nucleotide sequence is optimized：Shown in 36.

Third purpose of the present invention is to provide a kind of expression vector containing above-mentioned nucleotide sequence.

4th purpose of the invention is to provide a kind of recombinant host bacterium containing above-mentioned expression vector.

5th purpose of the invention is to provide a kind of method producing above-mentioned single-chain antibody, including：

1) above-mentioned recombinant host bacterium expression antibody is cultivated under suitable conditions；

2) it and then from host strain purifies, collect antibody.

The 6th of the present invention is designed to provide above-mentioned anti-human RBP ELISA antibody in detection human retinol knot Application in hop protein content.

The 7th of the present invention is designed to provide one group of antibody that can be matched and detect human retinol-binding protein To combination；And detection sensitivity is high, specificity is good.

The 8th of the present invention is designed to provide a kind of utilization anti-human RBP ELISA antibody test people and regards The protein-bonded colloidal gold immunochromatographimethod quantitative test card of flavol, including sample absorption pad, gold-labelled pad, reaction film and water absorption pad； The gold-labelled pad is coated with the antibody B14 of colloid gold particle label, there is detection band and quality control band, detection band position on the reaction film It sets and is coated with antibody B08, quality control band position is coated with anti-His tag antibodies or Protein L.The preferred cellulose nitrate of reaction film Plain film.The anti-anti- His antibody of the preferred mouse of His tag antibodies.

The present invention is prepared for a variety of monoclonal antibodies, and carries out pairing screening, and obtaining sensitivity and specificity can meet One group of antibody combination (B08 and B14) of demand；It facilitates mass production simultaneously, can meet the need of larger scale clinical application in the future It asks.It is detected the debugging Optimization Work of system to above-mentioned antibody combination, obtains easy to operate, sensitivity, specificity and correlation Detection performance can meet human blood or the colloidal gold immunochromatographimethod of the human retinol-binding protein of urine specimen detection quantitatively detects Card.

Description of the drawings

Fig. 1 antibody B08 and B14 heavy chains and chain variable region gene electrophoretogram.Lane 1 is that B08 light chain variable regions PCR expands Increase gene, Lane 2 is that 200DNA Ladder, Lane 3 are B08 heavy chain variable region PCR amplification genes, and Lane 4 is B14 light chains Variable region PCR amplification gene, Lane 5 are B14 heavy chain variable region PCR amplification genes.

Fig. 2 single-chain antibody structural schematic diagrams.V_HIndicate weight chain variabl area sequence, V_LIndicate light-chain variable sequence, His marks Label are six histidines.

Fig. 3 single-chain antibodies express the agarose gel electrophoresis figure of PCR product.Fig. 3-a are B08 gene PCR products；Fig. 3-b For B14 gene PCR products.

Fig. 4 single-chain antibody specific detections design sketch (Western Blot).Fig. 4-a are antibody B08；Fig. 4-b are antibody B14。

Fig. 5 colloidal gold immunochromatographimethod quantitative test card result schematic diagrams of the present invention.1 it is sample pad, 2 be reaction film, 3 is Absorption pad, 4 be nature controlling line (C lines), 5 be detection line (T lines), 6 be gold-labelled pad, 7 be PVC sheet.

Fig. 6 .RBP detection card (B08-B14) matched curve figures, wherein calibration curve equation is y=-2E-05x2+0.008x + 0.109, wherein coefficient R²=0.998.

Fig. 7 .RBP detection card (B08-B14) range of linearity figures, wherein calibration curve equation y=0.793x-3.347, Related coefficient is R²=0.980.

Fig. 8 .RBP detection card (B08-B14) methodologies compare

Specific implementation mode

Definition

" antibody " is also known as immunoglobulin, is a kind of large-scale Y shape protein secreted by bone-marrow-derived lymphocyte, can pass through Y shape Two of which bifurcated top complementary site (antigen knot bound site) specific binding target antigen immunoglobulin molecules, institute State target antigen such as protein, sugar, polynucleotides, fat, polypeptide, micromolecular compound etc..

" single-chain antibody " (scFv) refers to the heavy chain variable region (V of antibody_H) and light chain variable region (V_L) pass through 15~20 The single chain fusion protein that amino acid short peptide (linker) connection is formed, the linker for connection are generally rich in glycine and silk Propylhomoserin, in favor of the stability and flexibility of single-chain antibody.Connection type can be by V_LN-terminal be connected to V_HC-terminal, Huo Zhexiang Instead.Although eliminating constant region and introducing linker, single-chain antibody still remains specificity of the antibody to antigen, and it has Molecular weight is small, penetration power is strong and it is antigenic weak the features such as.

Complementary determining region (complementarity-determining region, CDR), also referred to as hypervariable region.Molding It is the most critical zone that target antigen is combined with antibody in the end of antibody monomer amino acid, in Artificial Immune Network Theory, Mei Gekang The complementary determining region of body is otherwise known as idiotype or genotype.

The preparation of 1. anti-human RBP ELISA hybridoma cell strain of embodiment

1. animal immune

Exempted from according to general immune programme with recombinating human retinol-binding protein (prepared by Recombinant protein expression, our company) Epidemic disease BALB/c female mices (are purchased from this experimental animal Co., Ltd of Changzhou Cavan).Specific Immunity referring to《Antibody preparation with Use experiment guide》.Immune serum titre is tracked using indirect elisa method, chooses the highest immune mouse of serum titer, It carries out mouse boosting cell and murine myeloma cell carries out fusion experiment.

2. cell fusion

(1) preparation of spleen cells

It by immune mouse, plucks eyeball and takes blood, put to death to be placed in the alcohol of 75% (v/v) through the cervical vertebra that breaks and impregnate 10 minutes, Its spleen is taken out in aseptic operating platform, is placed in cell screen clothes, cell is fully ground, and sieve is crossed, with sterile 1640 culture medium (be purchased from Gibco companies) centrifuge washing for several times after, cell is resuspended so that single cell suspension is made, and count, it is spare.

(2) preparation of feeder cells

Female BAl BIc/c the mouse one for taking 8~10 week old pluck eyeball and obtain negative serum, and postposition is put to death through disconnected cervical vertebra It is impregnated 10 minutes in 75% (v/v) alcohol；Sterile to open skin of abdomen, exposure peritonaeum will about 10mL 1640HT trainings with syringe Base (be purchased from SIGMA companies) injection mouse peritoneal is supported, gently abdomen massage and is blown and beaten for several times.Draw the culture containing macrophage Base injects spare in 20%1640HAT culture mediums；

Female BAl BIc/c the mouse one for taking 2~3 week old are placed in 75% (v/v) alcohol through disconnected cervical vertebra execution and impregnate 10 minutes；Sterile to take thymus gland in cell screen clothes, sieve is crossed in grinding, obtain thymocyte be placed in it is above-mentioned containing macrophage It is spare in 20%1640HAT culture mediums.

(3) cell fusions

Murine myeloma cell strain SP2/0 of the selection in exponential phase, collects and counts.Take about 10⁸A above-mentioned spleen Cell and 2 × 10⁷A above-mentioned SP2/0 cell strains, which are added in fusion pipe, to be mixed, and 1000rpm centrifugations abandon supernatant (as possible after ten minutes Abandon net), fusion pipe is set and is gently rubbed back and forth on palm so that precipitation is loose.1mL preheatings are added after elder generation is slow in 60 seconds soon PEG1450 (polyethylene glycol 1450 is purchased from SIGMA companies), is added 1640HT culture mediums 30mL and terminates, 1000rpm centrifuges 10 points Clock removes supernatant, and gently friction keeps precipitation loose, is added in the 20% 1640HAT culture mediums that step 2 is obtained.

It after above-mentioned HAT culture mediums are mixed well, is dispensed into 96 porocyte culture plates with 200 holes μ L/, sets 37 DEG C, 5% CO₂Cell incubator in cultivate.It uses 10%1640HT culture mediums to replace 20%1640HAT culture mediums after a week, is taken after 3 days It is detected clearly.

3. anti-human RBP ELISA specific hybrid tumor strain screening

(1) preparation of detection plates：With CB coating buffers dilute recombination human retinol-binding protein (E. coli system express, It is prepared by our company) to 1 μ g/mL, 96 hole ELISA ELISA Plates, 100 holes μ L/ are coated with, 2~8 DEG C of coatings overnight, washed once and pat dry； PBST buffer blinds (holes 200ul/) containing 2% bovine serum albumin(BSA), 37 DEG C are closed 2 hours；It pats dry, it is spare.

(2) screening of positive colonies：100 holes μ L/ of cells and supernatant to be checked are added in above-mentioned detection plate, in 37 DEG C Effect was washed and is patted dry after 30 minutes, and the sheep anti-mouse igg of the HRP labels in 100 holes μ L/ is added, is washed after being acted on 30 minutes in 37 DEG C It washs and pats dry, the TMB developing solutions in 100 holes μ L/ are added, colour developing 15 minutes is protected from light in 37 DEG C, the 2M H of 50 μ L are added per hole₂SO₄Eventually It only reacts, and the reading numerical values at OD450.Positive hole determines principle：OD450 values/negative control value >=2.1.Choose positive gram Grand strain carries out Cell-cloned screening.After three to four-wheel cloning screening, monoclonal cell strain positive rate 100% is i.e. true It is set to stable cell line, singling is carried out to cell strain.Hybridoma cell strain R08 and R14 all have higher potency, then subsequently into One step carries out antibody variable sequences sequencing analysis to above-mentioned hybridoma cell strain.

The measurement of 2. hybridoma cell strain antibody variable sequences of embodiment

Above-mentioned hybridoma cell strain R08 and the antibody variable sequences R14 are measured.

The extraction of a.RNA：Reference cell total serum IgE extraction agent box (being purchased from Roche companies) specification is to above-mentioned hybridoma Cell strain R08 and R14 carry out Total RNAs extraction and carry out reverse transcription immediately；

B.RNA reverse transcriptions become DNA：With reference to Thermo Scientific Reverted First strand cDNA Synthesis Kit (being purchased from Thermo companies) carry out reverse transcription to the total serum IgE extracted in previous step, and cDNA is made, freezes Be stored in -20 DEG C it is spare；

C. the PCR amplification of variable region sequences and recycling：Using gained cDNA is template in previous step, with mouse IgG hypotype lists Clonal antibody variable region sequences universal primer is primer, carries out PCR amplification to the variable region sequences of heavy chain and light chain, PCR is produced Object is recycled through DNA plastic recovery kits (being purchased from TIANGEN companies), sees attached drawing 1；

D. the clone of variable region sequences and sequencing：According to cloning vector pMD18-T kit (being purchased from Takara companies) Heavy chain and chain variable region gene are attached with pMD18-T carriers by specification respectively, convert bacillus coli DH 5 alpha, picking Positive colony transfers to Nanjing Genscript Biotechnology Co., Ltd. to be sequenced.

Sequencing obtains the antibody B08 heavy chain variable amino acids sequence such as SEQ ID NO of hybridoma cell strain R08:7 institutes Show, chain variable region amino acid sequence such as SEQ ID NO：Shown in 8.The above-mentioned sequence of Vbase2 database analysis, weight chain variable The amino acid sequence of each complementary determining region in area is respectively：Such as sequence SEQ ID NO：HCDR1 shown in 1, such as sequence SEQ ID NO：HCDR2 shown in 2 and/or such as sequence SEQ ID NO：HCDR3 shown in 3；Each complementary determining region of its light chain variable region Amino acid sequence is：Such as sequence SEQ ID NO：LCDR1 shown in 4, such as sequence SEQ ID NO：LCDR2 shown in 5 and/or such as Sequence SEQ ID NO：LCDR3 shown in 6.

Sequencing obtains the antibody B14 heavy chain variable amino acids sequence such as SEQ ID NO of hybridoma cell strain R14:15 institutes Show, chain variable region amino acid sequence such as SEQ ID NO：Shown in 16.The above-mentioned sequence of Vbase2 database analysis, weight chain variable The amino acid sequence of each complementary determining region in area is respectively：Such as sequence SEQ ID NO：HCDR1 shown in 9, such as sequence SEQ ID NO：HCDR2 shown in 10 and/or such as sequence SEQ ID NO：HCDR3 shown in 11；Each complementary determining region of its light chain variable region Amino acid sequence be：Such as sequence SEQ ID NO：LCDR1 shown in 12, such as sequence SEQ ID NO：LCDR2 shown in 13 and/ Or such as sequence SEQ ID NO：LCDR3 shown in 14.

The recombinant expression of 3. single-chain antibody of embodiment and purifying

According to sequencing result in embodiment 2, by the heavy chain of antibody of hybridoma cell strain R08 and R14 and light chain variable region it Between be added connection peptide (GGGGS)₃, six histidines are introduced, and the progress of its full genome is artificial synthesized, are building up in Pichia pastoris The recombinant expression of single-chain antibody is carried out, expressed obtained antibody is respectively designated as antibody B08 and B14, and structure composition is for example attached Shown in Fig. 2.The recombinant expression of above-mentioned single-chain antibody is specific as follows：

1. the expression plasmid of antigen-4 fusion protein gene is built

The gene order of antibody B08 after codon optimization such as SEQ ID NO:35 shown, amino acid sequence such as SEQ ID NO:Shown in 33；The gene order of antibody B14 after codon optimization such as SEQ ID NO:36 shown, amino acid sequence such as SEQ ID NO:Shown in 34.The genetic fragment upstream of artificial synthesized antibody B08, B14 are introduced into XhoI sequence enzymes in pPICZ α A carriers Enzyme site, downstream introduce XbaI enzyme cutting site, and it is (public purchased from Invitrogen to be building up to pMD19-T Simple Vector plasmids Department) in, a kind of long-term preservation plasmid is obtained, plasmid is denoted as pMD19-B08-scFv- (HIS)₆、pMD19-B14-scFv- (HIS)₆.PCR amplification is carried out, wherein sense primer P1 is CGCCAGGGTTTTCCCAGTCACGAC；Downstream primer P2 is: AGCGGATAACAATTTCACACAGGA.After Standard PCR program, agarose gel electrophoresis analyzes (attached drawing 3), shows primer size It is in the same size with expection.After PCR is obtained gene outcome recovery purifying respectively, using XhoI, (#R0146S is purchased from New England Biolabs companies) and XbaI (#R0145V is purchased from New England Biolabs companies) double digestion, connected with T4 Connect enzyme to be connected in pPICZ α A (V19520, be purchased from Invitrogen) plasmid, be transformed into DH5 α competent cells, containing 37 DEG C of overnight incubations in the LB tablets of Zeocin (R250-01 is purchased from Invitrogen companies).Second day screening positive clone bacterium Sequencing compares, completely the same to get to the expression plasmid of antibody B08, B14 with expected sequence, is denoted as pPICZ α-B08-scFv- (HIS)₆、pPICZα-B14-scFv-(HIS)₆。

2. antigen-4 fusion protein gene is in the structure of Pichia pastoris host's engineered strain, screening and expression

YPDS solid mediums are prepared：With reference to Invitrogen company EasySelectPichia Expression Kit Specification；Pichia pastoris competent cell：With reference to EasySelectPichia Expression Kit specifications；BMGY is cultivated Basigamy system：With reference to Invitrogen companies Multi-Copy Pichia Expression Kit specifications；BMMY culture mediums are matched System：With reference to Invitrogen companies Multi-Copy Pichia Expression Kit specifications.

Respectively by pPICZ α-B08-scFv- (HIS)₆、pPICZα-B14-scFv-(HIS)₆Plasmid, it is restricted interior with SacI Enzyme cutting linearization for enzyme restriction.By linearized vector after ethanol precipitation, electrotransformation enters X-33 competence yeast cells, is applied to and contains There are the YPDS solid mediums of Zeocin, 30 DEG C are cultivated 3-5 days, just there is positive colony generation.

The monoclonal of the above-mentioned acquisition of picking is in 5mL BMGY culture mediums, 30 DEG C of cultures to OD₆₀₀When=2.0~6.0, take 1mL preserves strain, and will be transferred to BMMY Small Amount induced expressions after the resuspension of remaining bacterium solution, dense to end every adding methanol for 24 hours Degree is 1% (v/v).After a week, supernatant of bacteria solution is collected by centrifugation, passes through PAGE gel electrophoresis and Western blot analysis (Western blot), object observing protein expression situation.Primary antibody is anti-HIS-Tag antibody (His-Tag in Western blot (2A8) Mouse mAb, M20001 is purchased from Ai Bimate biological medicines (Shanghai) Co., Ltd.).

B08 the and B14 recombination fusion protein engineering strains of above-mentioned acquisition are inoculated in BMGY culture mediums, 30 DEG C, 220rpm is cultivated to cell density to OD₆₀₀=2.0~6.0, methanol was added every 24 hours to final concentration of 1.0% (v/v). After a week, fermentation culture is collected.

3. fusion protein purification

Using histidine tag affinity column antibody purification B08 and B14 fusion protein, prepackage pillar is selected as HisTrap HP (17-5248-02 is purchased from GE healcare companies), is as follows：

The removal of impurities of zymotic fluid pre-processes：Above-mentioned expression is obtained into antibody B08 and B14 fusion protein fermented liquid supernatant, is centrifuged Supernatant is collected, and combination buffer is added so that supernatant final concentration of 300mMNaCl, 20mM NaH₂PO₄, 20mM Imidazole adjusts pH7.5,0.45 μm of membrane filtration.

Column purification that HisTrap HP are affine：With fully-automatic intelligent protein purification system, (AKTAavant150 is purchased from GE Healcare companies) affinity purification is carried out to antibody B08 and B14 the fusion protein zymotic fluid that pretreatment obtains, pillar is HisTrap HP.Combination buffer is 300mMNaCl, 20mMNaH₂PO₄, 20mM Imidazole, pH7.5, elution buffer is 300mMNaCl, 20mMNaH₂PO₄, 500mM Imidazole, pH7.5.Linear elution is carried out when elution, and collects each elution Peak.By SDS-PAGE electroresis appraisal purity, merge satisfactory collecting pipe, it is that simultaneously ultrafiltration is dense for PBS solution to replace buffer solution It contracts (1mg/mL), filtration sterilization is saved backup in -20 DEG C.

The performance evaluation of 4. antibody of embodiment

1. the Western blot identifications of antibody B08 and B14

A. polyacrylamide gel electrophoresis：12% separation gel, 5% concentration glue are configured, respectively loading standard protein and again Group human retinol-binding protein albumen (E. coli system is expressed, prepared by our company), electrophoresis 1 hour under constant pressure；

B. transferring film：Transferring film 1 hour under the conditions of constant current (35mA/ films), extremely by the Protein transfer on polyacrylamide gel On nitrocellulose filter.Coomassie brilliant blue G250 dyes the SDS-PAGE glue for completing transferring film, observes the residual feelings of albumen Condition；

C. it closes：TBST buffer blinds (confining liquid) containing 5% defatted milk, 4 DEG C overnight；Cleaning solution after closing (TBST, Refer to TaKaRa company's T BST buffer) it washed once, 10 minutes；

D. antigen-antibody reaction：Confining liquid dilution (presses 1:1000 volume ratios) horseradish peroxidase-labeled B08 (B08- HRP, 1mg/mL, our company are marked using classical Over-voltage protection, similarly hereinafter) and horseradish peroxidase-labeled B14 (B14-HRP, 1mg/mL, our company are marked using classical Over-voltage protection, similarly hereinafter), it is separately added into above-mentioned two nitrocellulose filters, room temperature Reaction 1 hour；TBST is washed 5 times, every time 10 minutes；

E. it develops the color and takes pictures：Residual liquid on nitrocellulose filter is blotted, 2mL stable type peroxides are added in nitrocellulose filter The mixed liquor (purchase is in Thermo companies) of compound enzyme solutions (1mL) and luminol/enhancing agent solution (1mL), uniform wet nitre The surface of acid cellulose film, room temperature are taken pictures after being protected from light one minute in gel imaging system (purchase is in GE companies), and knot is left and taken Fruit.

Testing result as it can be seen that antibody B08 and B14 all have preferable specificity, can specific detection human retinol combine Protein.

3. single-chain antibody B08 and B14 is in the evaluation of colloidal gold detection platform

The antibody purified in embodiment 3 is subjected to combinations of pairs, is matched respectively as coated antibody or labelled antibody RBP ELISA (RBP) is detected, detecting step is as follows：

1) B08 or B14 are diluted to 1mg/ml with antibody coating buffer, lined on nitrocellulose filter；

2) use 0.01M PB buffer solutions will be in spray and bonding pad after the B08 of colloid gold label or B14 dilutions；

3) pad pasting shown in attached drawing is pressed, slitting is loaded (specific to prepare referring to embodiment 5)

4) RBP standard items (Recombinant protein expression) are diluted with Sample dilution, until a concentration of 150mg/L, 16mg/L, The two concentration standards and zero standard's product (i.e. Sample dilution) are added in 50ul to colloidal-gold detecting-card respectively Detection card is placed on readout instrument after 10min and reads by (B08 coatings-B14 label or B14 coatings-B08 labels).As a result As shown in the table：

From the above results, it is seen that the double antibody sandwich method that B08 is formed as coated antibody, B14 as labelled antibody Detecting system can be applied to colloidal gold detection platform, carry out the detection of RBP.

The preparation of the colloid gold immune detection card of 5 anti-human RBP ELISA of embodiment

1, solution is prepared

1) prepared by 0.01M PB buffer solutions：Weigh Na₂HPO₄·12H₂O 3.22g, NaH₂PO₄·2H₂O 0.15g add pure Change water 1000ml, rotor is stirred to dissolving, its pH7.4 ± 0.1,0.45um membrane filtrations are measured with pH meter.

2) prepared by 0.01M PBS buffer solution：Weigh Na₂HPO₄1.44g KH₂PO₄0.24g, NaCl8g, KCl0.2g add pure Change water 1000ml, rotor is stirred to dissolving, its pH7.4 ± 0.1,0.45um membrane filtrations are measured with pH meter.

2) prepared by confining liquid：Bovine serum albumin(BSA) 5g is weighed, 0.01M PB solution (pH7.4 ± 0.1) 50ml, rotor is added to stir It mixes to dissolving.

3) prepared by antibody coating buffer：Take 0.05g bovine serum albumin(BSA)s, be added 10ml 0.01M PBS solutions (pH7.4 ± 0.1), rotor stirs 5-10min.

4) gold labeling antibody is redissolved liquid and is prepared：1g bovine serum albumin(BSA)s are weighed, it is molten that 100ml 0.01M PB are added in 5g trehaloses Liquid (pH7.4 ± 0.1), rotor is stirred to dissolving, and 25ul Tween-20 are added, and continues to stir 5-10min with rotor.

5) prepared by Sample dilution：500ml 0.01M PBS solutions (pH7.4 ± 0.1) are taken, 0.5ml is added Proclin300, rotor are stirred to dissolving.

2, prepared by human retinol-binding protein colloidal-gold detecting-card

1) label of colloidal gold

The colloid gold label of antibody B14 (by taking 1ml colloidal gold solutions label as an example)：Use K₂CO₃It is (every to adjust colloidal gold pH value 10ul 0.2M K are added in 1ml colloidal golds₂CO₃), it stirs 5-10 minutes, it is (every that antibody B14 is slowly added into colloidal gold solution 5ug antibody B14 are added in 1ml colloidal golds), stirring at low speed 30 minutes；Confining liquid BSA is added to its final concentration of 10% (quality Percentage), it stirs 20 minutes；12000rpm centrifuges 30min after standing 30min；Supernatant 100ul gold labeling antibodies are gone to redissolve liquid multiple The molten B14 antibody precipitated up to colloid gold label.

2) gold-labelled pad and reaction film preparation

B14 gold labeling antibodies are sprayed in gold-labelled pad 6, drying for standby；

After antibody B08 is diluted to 1.0mg/ml with antibody diluent, it is coated in the T of reaction film 2 (nitrocellulose filter) 5 position of line；After anti-His tag antibodies are diluted to 0.2mg/ml with antibody diluent, it is coated in 2 (nitrocellulose of reaction film Film) 4 position of C lines, reaction film drying for standby.

3) pad pasting, cut film, assembling

Sample pad 1, gold-labelled pad 6, the nitrocellulose filter 2 for being coated with antibody, water absorption pad 3 are set gradually from left to right (as shown in Figure 5), and should contact a little between any two, the T lines 5 of the nitrocellulose filter for being coated with antibody are in left, C lines 4 It is cut on the right side, and according to shell size, is packed into shell, it is standby to complete detection blocking.

4) kit assembles

Assembled detection is blocked, drier is fitted into aluminium foil bag, heat sealing machine sealing, labelling；

Sample dilution is dispensed by 1ml/ pipes, and valve bag, labelling are packed into according to kit specification；

According to trimmed size, by the interior packet of certain number, 1 valve bag containing Sample dilution, 1 part of specification, 1 conjunction Case marker label are packed into packing box, and label is posted outside packing box.

3, human retinol-binding protein colloidal-gold detecting-card application method

1) outer packing is opened, detection card is taken out from sealing aluminium foil bag, is placed on flat table.

2) 10 μ l serum/plasma samples are drawn, is added in Sample dilution A and is sufficiently mixed, therefrom draw 10ul mixed liquors It is added in B pipe Sample dilutions, is sufficiently mixed.

3) samples of 40ul after processing are drawn to be added in the well of detection card, stand 10min at room temperature.

4) detection card is put into immunochromatography quantitative analysis instrument, presses " quickly detection " key and start to detect, instrument will be automatic Detection card is scanned.

5) from reading/printing testing result on the display screen of immunochromatography quantitative analysis instrument.

4, human retinol-binding protein colloidal-gold detecting-card detection result is assessed

1) accuracy：B08 (coating)-B14 (label) detections card is detected 16,150mg/L's by detection card application method Each 10 replications of RBP reference materials calculate detection card precision after rejecting outlier.Experimental result shows three Concentration Testings As a result coefficient of variation CV<15%.

Concentration point (mg/L)	16	150
			CV	11.24%	8.56%

2) detection range：By B08 (coating)-B14 (label) detect card detection various concentration RBP recombinant proteins 5.625, 11.25,22.5,45,90,180mg/L, matched curve and detection range are 8-180mg/L (such as attached drawing 6).

3) range of linearity：High level sample and Sample dilution are configured to 5 series concentration samples according to a certain percentage, used Result and theoretical concentration are carried out regression calculation, sentenced by B08 (coating)-B14 (label) detection card detections, each pattern detection 3 times Break whether linear in the concentration range.The range of linearity is 8-180mg/L (such as attached drawing 7).

4) accuracy：B08 (coating)-B14 (label) detections card is detected 16,150mg/L's by detection card application method Each 3 repetitions of RBP reference materials, calculate the relative deviation of average value and theoretical value, and experimental result shows three Concentration Testing results Relative deviation B<15%.

Concentration point (mg/L)	16	150
			B	9.78%	5.67%

5, accuracy-methodology compares：

Chongqing Zhongyuan Biological Technology Co., Ltd.'s retinol of good prestige is obtained in selection similar product currently on the market Binding protein assay kit (latex enhancing immune turbidimetry) compares product comparison verification.Select 30 parts of clinical patient marks This, by 1 to 30 serial number, the colloidal-gold detecting-card with reference product and B08 to be evaluated (coating)-B14 (label) is same Shi Jinhang is tested, and is measured according to 1,2,3......28,29,30,30,29,28......3,2,1 sample order.Control With the testing result coefficient R of product to be evaluated²=0.99, illustrate that two methods testing result has preferable correlation (such as Attached drawing 8).

5, recipe determination

In addition to above-mentioned optimal preparation example 1, applicant also attempts a variety of preparation methods, for example, several groups of detection blockings below it is standby and Using result such as following table：

Sequence table

<110>Jiangsu Jiangsu Zhonghong Biopharma Institute Inc. of crystalline substance red-face role's object medical sci-tech limited liability company

<120>People RBP colloidal gold immunochromatographimethod quantitative testing test paper cards and its clinical application

<160> 36

<170> SIPOSequenceListing 1.0

<210> 1

<211> 8

<212> PRT

<213> mus musculus

<400> 1

Gly Tyr Ser Phe Thr Arg Tyr Tyr

1 5

<210> 2

<211> 8

<212> PRT

<213> Mus musculus

<400> 2

Ile Phe Pro Gly Ser Gly Asn Thr

1 5

<210> 3

<211> 17

<212> PRT

<213> Mus musculus

<400> 3

Ala Arg Ser Pro Pro Leu Tyr Phe Gly Asn Tyr Glu Gly Ala Met Asp

1 5 10 15

Tyr

<210> 4

<211> 7

<212> PRT

<213> Mus musculus

<400> 4

Ser Ser Val Asn Ser Ser Tyr

1 5

<210> 5

<211> 3

<212> PRT

<213> Mus musculus

<400> 5

Ser Thr Ser

1

<210> 6

<211> 9

<212> PRT

<213> Mus musculus

<400> 6

His Gln Tyr His Arg Ser Pro Leu Thr

1 5

<210> 7

<211> 124

<212> PRT

<213> Mus musculus

<400> 7

Gln Val Gln Leu Gln Gln Ser Gly Pro Glu Leu Val Lys Pro Gly Ala

1 5 10 15

Ser Val Lys Ile Ser Cys Lys Ala Ser Gly Tyr Ser Phe Thr Arg Tyr

20 25 30

Tyr Ile His Trp Val Lys Gln Arg Pro Gly Gln Gly Leu Glu Trp Ile

35 40 45

Gly Trp Ile Phe Pro Gly Ser Gly Asn Thr Glu Tyr Ser Glu Met Phe

50 55 60

Lys Asp Lys Ala Thr Leu Thr Ala Asp Thr Ser Ser Ser Thr Ala Tyr

65 70 75 80

Met Gln Leu Ser Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Phe Cys

85 90 95

Ala Arg Ser Pro Pro Leu Tyr Phe Gly Asn Tyr Glu Gly Ala Met Asp

100 105 110

Tyr Trp Gly Gln Gly Thr Ser Val Thr Val Ser Ala

115 120

<210> 8

<211> 108

<212> PRT

<213> Mus musculus

<400> 8

Gln Ile Val Leu Thr His Ser Pro Pro Ile Met Ser Ala Ser Leu Gly

1 5 10 15

Glu Arg Val Thr Met Thr Cys Thr Ala Asn Ser Ser Val Asn Ser Ser

20 25 30

Tyr Leu His Trp Tyr Gln Gln Lys Pro Gly Ser Ser Pro Lys Leu Trp

35 40 45

Ile Tyr Ser Thr Ser Asn Leu Ala Ser Gly Val Pro Ala Arg Phe Ser

50 55 60

Gly Ser Gly Ser Gly Thr Ser Tyr Ser Leu Thr Ile Thr Ser Met Glu

65 70 75 80

Ala Glu Asp Ala Ala Thr Tyr Tyr Cys His Gln Tyr His Arg Ser Pro

85 90 95

Leu Thr Phe Gly Ala Gly Thr Lys Leu Glu Ile Lys

100 105

<210> 9

<211> 8

<212> PRT

<213> Mus musculus

<400> 9

Gly Tyr Arg Phe Thr Asp Tyr Trp

1 5

<210> 10

<211> 8

<212> PRT

<213> Mus musculus

<400> 10

Ile Asp Gly Tyr Asp Ser Glu Thr

1 5

<210> 11

<211> 14

<212> PRT

<213> Mus musculus

<400> 11

Ala Arg Ser Gly Ala Val Glu Gly Arg Tyr Ser Met Asp Tyr

1 5 10

<210> 12

<211> 10

<212> PRT

<213> Mus musculus

<400> 12

Glu Ser Val His Ser Tyr Gly His Ser Phe

1 5 10

<210> 13

<211> 3

<212> PRT

<213> Mus musculus

<400> 13

Arg Ala Ser

1

<210> 14

<211> 9

<212> PRT

<213> Mus musculus

<400> 14

Gln Gln Ser Asn Glu Asp Pro Arg Thr

1 5

<210> 15

<211> 121

<212> PRT

<213> Mus musculus

<400> 15

Gln Val Gln Leu Gln Gln Pro Gly Ala Glu Leu Val Arg Pro Gly Thr

1 5 10 15

Ser Val Lys Leu Ser Cys Lys Ala Ser Gly Tyr Arg Phe Thr Asp Tyr

20 25 30

Trp Met Asn Trp Val Lys Gln Arg Pro Asp Gln Gly Leu Glu Trp Ile

35 40 45

Gly Arg Ile Asp Gly Tyr Asp Ser Glu Thr His Tyr Thr Gln Tyr Phe

50 55 60

Arg Asp Lys Ala Met Leu Thr Val Asp Lys Ser Ser Ser Thr Ala Tyr

65 70 75 80

Met Gln Leu Ser Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Tyr Cys

85 90 95

Ala Arg Ser Gly Ala Val Glu Gly Arg Tyr Ser Met Asp Tyr Trp Gly

100 105 110

Gln Gly Thr Ser Val Thr Val Ser Ser

115 120

<210> 16

<211> 111

<212> PRT

<213> Mus musculus

<400> 16

Asp Ile Val Leu Thr Gln Ser Pro Ala Ser Leu Ala Val Ser Leu Gly

1 5 10 15

Gln Arg Ala Thr Val Ser Cys Arg Ala Ser Glu Ser Val His Ser Tyr

20 25 30

Gly His Ser Phe Met His Trp Tyr Arg Gln Lys Pro Gly Gln Pro Pro

35 40 45

Lys Leu Leu Ile Tyr Arg Ala Ser Asn Leu Glu Ser Gly Ile Pro Val

50 55 60

Arg Phe Thr Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Asn

65 70 75 80

Pro Val Glu Ala Asp Asp Val Ala Thr Tyr Tyr Cys Gln Gln Ser Asn

85 90 95

Glu Asp Pro Arg Thr Phe Gly Gly Gly Thr Lys Leu Glu Ile Lys

100 105 110

<210> 17

<211> 24

<212> DNA

<213> Mus musculus

<400> 17

ggctacagct tcacaaggta ctat 24

<210> 18

<211> 24

<212> DNA

<213> Mus musculus

<400> 18

atttttcctg gaagtggtaa tact 24

<210> 19

<211> 51

<212> DNA

<213> Mus musculus

<400> 19

gcaagaagcc cccccctcta ctttggtaac tacgaggggg ctatggacta c 51

<210> 20

<211> 21

<212> DNA

<213> Mus musculus

<400> 20

tcaagtgtaa attccagtta c 21

<210> 21

<211> 9

<212> DNA

<213> Mus musculus

<400> 21

agcacatcc 9

<210> 22

<211> 27

<212> DNA

<213> Mus musculus

<400> 22

accagtatca tcgttccccg ctcacgt 27

<210> 23

<211> 372

<212> DNA

<213> Mus musculus

<400> 23

caggtccagc tgcagcagtc tggacctgag ctggtgaagc ctggggcttc agtgaagata 60

tcctgcaagg cttctggcta cagcttcaca aggtactata tacactgggt gaagcagagg 120

cctggacagg gacttgagtg gattggatgg atttttcctg gaagtggtaa tactgagtac 180

agtgagatgt tcaaggacaa ggccacactg acggcagaca catcctccag cacagcctac 240

atgcagctca gcagcctgac atctgaggac tctgcagtct atttctgtgc aagaagcccc 300

cccctctact ttggtaacta cgagggggct atggactact ggggtcaagg aacctcagtc 360

accgtctccg ca 372

<210> 24

<211> 325

<212> DNA

<213> Mus musculus

<400> 24

caaattgttc tcacccattc tccaccaatc atgtctgcat ctctagggga acgggtcacc 60

atgacctgca ctgccaactc aagtgtaaat tccagttact tgcactggta ccagcagaag 120

ccaggatcct cccccaaact ctggatttat agcacatcca acctggcttc tggagtccca 180

gcccgcttca gtggcagtgg gtctgggacc tcttactctc tcacaatcac cagcatggag 240

gctgaagatg ctgccactta ttactgccac cagtatcatc gttccccgct cacgttcggt 300

gctgggacca agctggaaat caaac 325

<210> 25

<211> 24

<212> DNA

<213> Mus musculus

<400> 25

ggctacaggt tcaccgacta ctgg 24

<210> 26

<211> 24

<212> DNA

<213> Mus musculus

<400> 26

attgatggtt acgatagtga aact 24

<210> 27

<211> 42

<212> DNA

<213> Mus musculus

<400> 27

gcaagatctg gggcagtaga agggaggtat tctatggact ac 42

<210> 28

<211> 30

<212> DNA

<213> Mus musculus

<400> 28

gaaagtgttc atagttatgg ccatagtttt 30

<210> 29

<211> 9

<212> DNA

<213> Mus musculus

<400> 29

cgtgcatcc 9

<210> 30

<211> 27

<212> DNA

<213> Mus musculus

<400> 30

aacaaagtaa tgaagatcct cggacgt 27

<210> 31

<211> 363

<212> DNA

<213> Mus musculus

<400> 31

caggtccaac tgcagcagcc tggggctgaa ttggtgaggc ctgggacttc tgtgaaactg 60

tcctgcaagg cttctggcta caggttcacc gactactgga tgaactgggt taagcagagg 120

cctgaccaag gccttgagtg gattggaagg attgatggtt acgatagtga aactcactac 180

actcaatact tcagggacaa ggccatgttg actgtagaca agtcctccag cacagcctac 240

atgcaactca gcagcctgac atctgaggac tctgcggtct attactgtgc aagatctggg 300

gcagtagaag ggaggtattc tatggactac tggggtcaag gaacctcagt cactgtctcc 360

tca 363

<210> 32

<211> 334

<212> DNA

<213> Mus musculus

<400> 32

gacattgtgc tgacccagtc tccagcttct ttggctgtgt ctctagggca gagggccacc 60

gtatcctgca gagccagtga aagtgttcat agttatggcc atagttttat gcactggtac 120

cggcagaaac caggacagcc acccaaactc ctcatctatc gtgcatccaa tcttgaatct 180

gggatccctg tcaggttcac tggcagtggg tctgggacag acttcaccct caccattaat 240

cctgtggagg ctgatgatgt tgcaacctat tactgtcaac aaagtaatga agatcctcgg 300

acgttcggtg gaggcaccaa gttggaaata aaac 334

<210> 33

<211> 247

<212> PRT

<213> Mus musculus

<400> 33

Gln Val Gln Leu Gln Gln Ser Gly Pro Glu Leu Val Lys Pro Gly Ala

1 5 10 15

Ser Val Lys Ile Ser Cys Lys Ala Ser Gly Tyr Ser Phe Thr Arg Tyr

20 25 30

Tyr Ile His Trp Val Lys Gln Arg Pro Gly Gln Gly Leu Glu Trp Ile

35 40 45

Gly Trp Ile Phe Pro Gly Ser Gly Asn Thr Glu Tyr Ser Glu Met Phe

50 55 60

Lys Asp Lys Ala Thr Leu Thr Ala Asp Thr Ser Ser Ser Thr Ala Tyr

65 70 75 80

Met Gln Leu Ser Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Phe Cys

85 90 95

Ala Arg Ser Pro Pro Leu Tyr Phe Gly Asn Tyr Glu Gly Ala Met Asp

100 105 110

Tyr Trp Gly Gln Gly Thr Ser Val Thr Val Ser Ala Gly Gly Gly Gly

115 120 125

Ser Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gln Ile Val Leu Thr

130 135 140

His Ser Pro Pro Ile Met Ser Ala Ser Leu Gly Glu Arg Val Thr Met

145 150 155 160

Thr Cys Thr Ala Asn Ser Ser Val Asn Ser Ser Tyr Leu His Trp Tyr

165 170 175

Gln Gln Lys Pro Gly Ser Ser Pro Lys Leu Trp Ile Tyr Ser Thr Ser

180 185 190

Asn Leu Ala Ser Gly Val Pro Ala Arg Phe Ser Gly Ser Gly Ser Gly

195 200 205

Thr Ser Tyr Ser Leu Thr Ile Thr Ser Met Glu Ala Glu Asp Ala Ala

210 215 220

Thr Tyr Tyr Cys His Gln Tyr His Arg Ser Pro Leu Thr Phe Gly Ala

225 230 235 240

Gly Thr Lys Leu Glu Ile Lys

245

<210> 34

<211> 247

<212> PRT

<213> Mus musculus

<400> 34

Gln Val Gln Leu Gln Gln Pro Gly Ala Glu Leu Val Arg Pro Gly Thr

1 5 10 15

Ser Val Lys Leu Ser Cys Lys Ala Ser Gly Tyr Arg Phe Thr Asp Tyr

20 25 30

Trp Met Asn Trp Val Lys Gln Arg Pro Asp Gln Gly Leu Glu Trp Ile

35 40 45

Gly Arg Ile Asp Gly Tyr Asp Ser Glu Thr His Tyr Thr Gln Tyr Phe

50 55 60

Arg Asp Lys Ala Met Leu Thr Val Asp Lys Ser Ser Ser Thr Ala Tyr

65 70 75 80

Met Gln Leu Ser Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Tyr Cys

85 90 95

Ala Arg Ser Gly Ala Val Glu Gly Arg Tyr Ser Met Asp Tyr Trp Gly

100 105 110

Gln Gly Thr Ser Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly Gly

115 120 125

Gly Gly Ser Gly Gly Gly Gly Ser Asp Ile Val Leu Thr Gln Ser Pro

130 135 140

Ala Ser Leu Ala Val Ser Leu Gly Gln Arg Ala Thr Val Ser Cys Arg

145 150 155 160

Ala Ser Glu Ser Val His Ser Tyr Gly His Ser Phe Met His Trp Tyr

165 170 175

Arg Gln Lys Pro Gly Gln Pro Pro Lys Leu Leu Ile Tyr Arg Ala Ser

180 185 190

Asn Leu Glu Ser Gly Ile Pro Val Arg Phe Thr Gly Ser Gly Ser Gly

195 200 205

Thr Asp Phe Thr Leu Thr Ile Asn Pro Val Glu Ala Asp Asp Val Ala

210 215 220

Thr Tyr Tyr Cys Gln Gln Ser Asn Glu Asp Pro Arg Thr Phe Gly Gly

225 230 235 240

Gly Thr Lys Leu Glu Ile Lys

245

<210> 35

<211> 742

<212> DNA

<213> Mus musculus

<400> 35

caggtccagc tgcagcagtc tggacctgag ctggtgaagc ctggggcttc agtgaagata 60

tcctgcaagg cttctggcta cagcttcaca aggtactata tacactgggt gaagcagagg 120

cctggacagg gacttgagtg gattggatgg atttttcctg gaagtggtaa tactgagtac 180

agtgagatgt tcaaggacaa ggccacactg acggcagaca catcctccag cacagcctac 240

atgcagctca gcagcctgac atctgaggac tctgcagtct atttctgtgc aagaagcccc 300

cccctctact ttggtaacta cgagggggct atggactact ggggtcaagg aacctcagtc 360

accgtctccg caggtggcgg agggtctggt ggcggagggt ccggtggcgg agggtcacaa 420

attgttctca cccattctcc accaatcatg tctgcatctc taggggaacg ggtcaccatg 480

acctgcactg ccaactcaag tgtaaattcc agttacttgc actggtacca gcagaagcca 540

ggatcctccc ccaaactctg gatttatagc acatccaacc tggcttctgg agtcccagcc 600

cgcttcagtg gcagtgggtc tgggacctct tactctctca caatcaccag catggaggct 660

gaagatgctg ccacttatta ctgccaccag tatcatcgtt ccccgctcac gttcggtgct 720

gggaccaagc tggaaatcaa ac 742

<210> 36

<211> 742

<212> DNA

<213> Mus musculus

<400> 36

caggtccaac tgcagcagcc tggggctgaa ttggtgaggc ctgggacttc tgtgaaactg 60

tcctgcaagg cttctggcta caggttcacc gactactgga tgaactgggt taagcagagg 120

cctgaccaag gccttgagtg gattggaagg attgatggtt acgatagtga aactcactac 180

actcaatact tcagggacaa ggccatgttg actgtagaca agtcctccag cacagcctac 240

atgcaactca gcagcctgac atctgaggac tctgcggtct attactgtgc aagatctggg 300

gcagtagaag ggaggtattc tatggactac tggggtcaag gaacctcagt cactgtctcc 360

tcaggtggcg gagggtctgg tggcggaggg tccggtggcg gagggtcaga cattgtgctg 420

acccagtctc cagcttcttt ggctgtgtct ctagggcaga gggccaccgt atcctgcaga 480

gccagtgaaa gtgttcatag ttatggccat agttttatgc actggtaccg gcagaaacca 540

ggacagccac ccaaactcct catctatcgt gcatccaatc ttgaatctgg gatccctgtc 600

aggttcactg gcagtgggtc tgggacagac ttcaccctca ccattaatcc tgtggaggct 660

gatgatgttg caacctatta ctgtcaacaa agtaatgaag atcctcggac gttcggtgga 720

ggcaccaagt tggaaataaa ac 742

Claims

1. human retinol-binding protein colloidal gold immunochromatographimethod quantitative test card, including sample absorption pad, gold-labelled pad, reaction film and Water absorption pad；The gold-labelled pad is coated with the antibody B14 of colloid gold particle label, there is detection band and quality control band on the reaction film, Detection band position is coated with antibody B08,

The antibody B08, heavy chain variable region contain complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：1 Shown in HCDR1, such as sequence SEQ ID NO：HCDR2 shown in 2, and/or such as sequence SEQ ID NO：HCDR3 shown in 3；With And its light-chain variable sequence contains complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：Shown in 4 LCDR1, such as sequence SEQ ID NO：LCDR2 shown in 5, and/or such as sequence SEQ ID NO：LCDR3 shown in 6；

The antibody B14, heavy chain variable region contain complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：9 Shown in HCDR1, such as sequence SEQ ID NO：HCDR2 shown in 10, and/or such as sequence SEQ ID NO：HCDR3 shown in 11； And its light-chain variable sequence contains complementary determining region below：Amino acid sequence such as sequence SEQ ID NO：Shown in 12 LCDR1, such as sequence SEQ ID NO：LCDR2 shown in 13, and/or such as sequence SEQ ID NO：LCDR3 shown in 14.

2. human retinol-binding protein colloidal gold immunochromatographimethod quantitative test card described in claim 1, the antibody B08 heavy chains The amino acid sequence of variable region such as SEQ ID NO:Shown in 7；The amino acid sequence of light chain variable region such as SEQ ID NO:Shown in 8.

3. human retinol-binding protein colloidal gold immunochromatographimethod quantitative test card described in claim 1, the antibody B14 heavy chains The amino acid sequence of variable region such as SEQ ID NO:Shown in 15；The amino acid sequence of light chain variable region such as SEQ ID NO:16 institutes Show.

4. human retinol-binding protein colloidal gold immunochromatographimethod quantitative test card described in claim 1, the antibody B08 is single Chain antibody, amino acid sequence such as SEQ ID NO:Shown in 33.

5. human retinol-binding protein colloidal gold immunochromatographimethod quantitative test card described in claim 1, the antibody B14 is single Chain antibody, amino acid sequence such as SEQ ID NO:Shown in 34.

6. claim 1-5 any one of them human retinol-binding protein colloidal gold immunochromatographimethod quantitative test cards, feature It is：It is the PB buffer solutions that 1~10%BSA is dissolved in 0.01M, pH7.4 ± 0.1 to prepare detection card confining liquid used.

7. according to claim 1-5 any one of them human retinol-binding protein colloidal gold immunochromatographimethod quantitative test cards, It is characterized in that：It is that 1%-10%BSA, 5% trehalose and 0.025% Tween-20 are molten to prepare detection card antibody used to redissolve liquid In the PB buffer solutions of 0.01M, pH7.4 ± 0.1.

8. according to claim 1-5 any one of them human retinol-binding protein colloidal gold immunochromatographimethod quantitative test cards, It is characterized in that：It is the PB buffer solutions that 0.5%BSA is dissolved in 0.01M, pH7.4 ± 0.1 to prepare detection card antibody coating buffer used.

9. according to claim 1-5 any one of them human retinol-binding protein colloidal gold immunochromatographimethod quantitative test cards, It is characterized in that：The Sample dilution of detection is that 0~2.5% BSA, 0.01~0.1% Proclin300 are dissolved in 0.01M's Borate buffer, pH7.4 ± 0.1.

10. claim 1-5 any one of them human retinol-binding protein colloidal gold immunochromatographimethod quantitative test cards are detecting The clinical application of human retinol-binding protein.