CN114075281A

CN114075281A - anti-Inhibin-alpha protein monoclonal antibody, cell line, preparation method and application thereof

Info

Publication number: CN114075281A
Application number: CN202111356411.0A
Authority: CN
Inventors: 李恢波; 吴茂; 王小亚; 邓晓; 黄信超; 李玲玲
Original assignee: Fuzhou Maixin Biotech Co ltd
Current assignee: Fuzhou Maixin Biotech Co ltd
Priority date: 2021-11-16
Filing date: 2021-11-16
Publication date: 2022-02-22
Anticipated expiration: 2041-11-16
Also published as: CN114075281B

Abstract

The invention relates to the field of biological detection, and provides an anti-Inhibin-alpha protein monoclonal antibody, wherein the amino acid sequences of the heavy chain and light chain variable regions are respectively the amino acid sequences shown in SEQ ID NO.2 and SEQ ID NO. 3. The inventor also provides a hybridoma cell line for secreting anti-Inhibin-alpha protein, wherein the cell line is a mouse hybridoma cell line 15E11D5E11 with the preservation number of: CGMCC NO. 22320. The anti-Inhibin-alpha protein monoclonal antibody has high specificity and sensitivity, can specifically identify cells expressing Inhibin-alpha protein, and is suitable for immunological detection, especially immunohistochemical detection.

Description

anti-Inhibin-alpha protein monoclonal antibody, cell line, preparation method and application thereof

Technical Field

The invention relates to the field of biological detection, in particular to an Inhibin-alpha protein resisting monoclonal antibody, a cell line, a preparation method and application thereof.

Background

Inhibin is one of the important hormones regulated by the hypothalamic pituitary gonadal axis system. Inhibin belongs to a member of TGF-beta family, and can inhibit synthesis and secretion of adenohypophysis anterior lobe basic and FSH regulated by gonadotropin-releasing hormone by reducing transcription of follicle stimulating hormone gene and down-regulating gonadotropin-releasing hormone receptor in paracrine and autocrine manner. And has local regulating effect on gonadal steroid production. Inhibin consists essentially of inhibin A and inhibin B, both of which have alpha subunits, differing in the form of beta subunits. The Inhibin-alpha subunit has only one molecular structure, a relative molecular mass of 18000, and is located on human chromosome 2q 33.

Inhibin-alpha is produced by Sertoli cells and ovarian granulosa cells of the testis and inhibits the production and secretion of pituitary gonadotropins. Inhibin-alpha is obviously increased in most ovarian epithelial cancers, is more obviously increased in granulocytoma and mucinous cystadenocarcinoma, has higher expression in the early stage of ovarian malignant tumor, and is commonly used for differential diagnosis of ovarian granulocytoma and cancer. In addition, Inhibina is expressed in normal adrenal cortex, cortical nodular hyperplasia and cortical tumor, mainly expressed in the inner layer of the reticular zone and fasciculate zone of the cortex, and is mainly expressed in the cortical tumor (particularly cortical adenoma) in a diffuse way, thereby being helpful for judging normal or hyperplastic tissue or tumor tissue.

Disclosure of Invention

The inventor provides an anti-Inhibin-alpha protein monoclonal antibody, and the amino acid sequences of heavy chain and light chain variable regions of the monoclonal antibody are respectively shown as SEQ ID NO.2 and SEQ ID NO. 3.

Furthermore, the heavy chain and light chain variable region amino acid sequences of the monoclonal antibody are respectively encoded by the nucleotide sequences shown in SEQ ID NO.4 and SEQ ID NO. 5.

Furthermore, in the preparation process of the monoclonal antibody, an antigen used by an immunized mouse is a recombinant protein which is coded by a nucleotide sequence shown in SEQ ID NO.1 and is expressed by escherichia coli recombination.

Further, the monoclonal antibody specifically recognizes the human Inhibin-alpha protein.

Further, the monoclonal antibody is produced by a hybridoma cell line with the preservation number of CGMCC NO. 22320. The cell line is a mouse hybridoma cell line 15E11D5E11, and is classified and named as: a mouse hybridoma cell line which has been deposited at 29.29.04 in 2021 at the center of China Committee for culture Collection of microorganisms and is addressed to the institute of microorganisms of the national academy of sciences, China, institute of sciences, No.3, West Lu 1, Beijing, Chaoyang, and the quarter.

Further, the anti-Inhibin-alpha protein is a mouse IgG1 subtype monoclonal antibody.

The inventor also provides a preparation method of the anti-Inhibin-alpha protein monoclonal antibody, and an antigen used by an immune mouse is a recombinant protein which is coded by a nucleotide sequence shown in SEQ ID NO.1 and is expressed by escherichia coli recombination.

The inventor also provides a hybridoma cell line for secreting anti-Inhibin-alpha protein, wherein the cell line is a mouse hybridoma cell line 15E11D5E11, the cell line is preserved in China general microbiological culture Collection center with the preservation number of: CGMCC NO. 22320.

The inventor also provides the application of the anti-Inhibin-alpha protein monoclonal antibody in human Inhibin-alpha protein immunoassay.

Further, the immunodetection includes immunohistochemistry, immunoblotting and enzyme-linked immunoassay.

The inventor further provides a human Inhibin-alpha protein immunoassay reagent, and the immunoassay reagent contains any one of the above Inhibin-alpha protein monoclonal antibodies as an effective component.

Different from the prior art, the technical scheme is that according to the structure, antigenicity, hydrophilicity and hydrophobicity of constituent amino acids and a secondary structure of the Inhibin-alpha protein, amino acid fragments from the 128 th site to the 300 th site of the Inhibin-alpha protein and corresponding nucleotide fragments are selected, recombinant expression is carried out through escherichia coli, immunization is carried out on a mouse, cell fusion, screening and cloning are carried out, a monoclonal cell line 15E11D5E11 which efficiently secretes the anti-Inhibin-alpha protein monoclonal antibody is obtained, the monoclonal cell line 15E11D5E11 is cultured in vitro, and the anti-Inhibin-alpha protein monoclonal antibody secreted by the cell line is obtained. The antibody obtained by the scheme has high specificity and sensitivity, can specifically recognize cells expressing Inhibin-alpha protein, and is suitable for immunological detection, particularly immunohistochemical detection.

The above description of the present invention is only an overview of the technical solutions of the present application, and in order to make the technical solutions of the present application more clearly understood by those skilled in the art, the present invention may be further implemented according to the content described in the text and drawings of the present application, and in order to make the above objects, other objects, features, and advantages of the present application more easily understood, the following description is made in conjunction with the detailed description of the present application and the drawings.

Drawings

FIG. 1 is a graph showing the results of electrophoresis of the purified Inhibin-alpha monoclonal antibody of example 3; m: and (4) marking molecular weight.

FIG. 2 immunoblot of detection of human Inhibin-alpha protein by Inhibin-alpha mab.

FIG. 3 is a graph showing immunohistochemical staining results for ovarian solitary stromal tumors.

Detailed Description

In order to explain in detail possible application scenarios, technical principles, practical embodiments, and the like of the present application, the following detailed description is given with reference to the accompanying drawings in conjunction with the listed embodiments. The embodiments described herein are merely for more clearly illustrating the technical solutions of the present application, and therefore, the embodiments are only used as examples, and the scope of the present application is not limited thereby.

Reference herein to "an embodiment" means that a particular feature, structure, or characteristic described in connection with the embodiment can be included in at least one embodiment of the application. The appearances of the phrase "an embodiment" in various places in the specification are not necessarily all referring to the same embodiment, nor are separate or related to other embodiments specifically defined. In principle, in the present application, the technical features mentioned in the embodiments can be combined in any manner to form a corresponding implementable technical solution as long as there is no technical contradiction or conflict.

Unless defined otherwise, technical terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this application belongs; the use of relational terms herein is intended only to describe particular embodiments and is not intended to limit the present application.

In the description of the present application, the term "and/or" is a expression for describing a logical relationship between objects, meaning that three relationships may exist, for example a and/or B, meaning: there are three cases of A, B, and both A and B. In addition, the character "/" herein generally indicates that the former and latter associated objects are in a logical relationship of "or".

In this application, terms such as "first" and "second" are used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions.

Without further limitation, in this application, the use of "including," "comprising," "having," or other similar expressions in phrases and expressions of "including," "comprising," or "having," is intended to cover a non-exclusive inclusion, and such expressions do not exclude the presence of additional elements in a process, method, or article that includes the recited elements, such that a process, method, or article that includes a list of elements may include not only those elements but also other elements not expressly listed or inherent to such process, method, or article.

As is understood in the examination of the guidelines, the terms "greater than", "less than", "more than" and the like in this application are to be understood as excluding the number; the expressions "above", "below", "within" and the like are understood to include the present numbers. In addition, in the description of the embodiments of the present application, "a plurality" means two or more (including two), and expressions related to "a plurality" similar thereto are also understood, for example, "a plurality of groups", "a plurality of times", and the like, unless specifically defined otherwise.

EXAMPLE 1 preparation of recombinant Inhibin-alpha protein fragments

First, antigen fragment selection

The Inhibin-alpha protein sequence with the number P05111 was selected as the standard sequence from the Uniprot database (http:// www.uniprot.org). The invention selects the 128 th to 300 th amino acid segments of human Inhibin-alpha protein as antigen, and designs the specificity upstream Primer 5 'GGATCCTCTGCCCAGCTGTGGTTTCATAC' (SEQ ID NO.6 restriction enzyme site, BamH I) and downstream Primer of the Inhibin-alpha protein by using software Primer 5.0 according to the corresponding base sequence (SEQ ID NO. 1): 5 'TATCTCGAGCGGGATGTGCAGACCAC 3' (SEQ ID NO.7, restriction site, Xho I), reverse transcription amplifying the gene fragment SEQ ID NO.1 encoding amino acids 128 to 300.

And separating the PCR product by agarose gel electrophoresis, recovering, carrying out BamH I and Xho I double enzyme digestion on the recovered target gene and a plasmid vector pET28a for expression, carrying out electrophoresis recovery again, and connecting by using T4 DNA ligase. And transforming the connecting product into an escherichia coli competent cell Rosetta, selecting clone on a plate, inoculating, expanding and culturing, extracting plasmid DNA, and performing PCR identification. The clone with positive target gene shown by PCR is sequenced and analyzed, and the clone with completely correct sequence is used for the next step.

Second, expression and purification of recombinant Inhibin-alpha protein fragment

Take out 100ul of competent cells (Rosetta) preserved at-80 deg.C, thaw, add 5ul of Inhibin-alpha plasmid DNA, and stand on ice for 30 min. After heat shock at 42 ℃ for 90 seconds and ice bath for 5min, 800. mu.L of non-resistant LB medium was added. Recovering and culturing at 37 deg.C for 60min, plating, and culturing overnight. The transformed plate was picked up and single colonies were cultured in 4ml of LB liquid medium overnight at 37 ℃ and 200rpm, and then the cells were maintained.

4ul of the bacterial liquid is taken to be put into 4ml of LB liquid culture medium and cultured overnight for recovery. The cultured bacterial suspension was transferred to 200ml of LB liquid medium, mixed, cultured at 37 ℃ and 200rpm until OD becomes 0.6-0.8, and then IPTG (0.5mM) was added thereto for overnight induction at low temperature. The cells were collected by centrifugation in a 400ml large centrifuge bowl at 4000rpm for 10min and the supernatant was discarded. The pellet was blown off with 20-30ml of 10mM Tris-HCl (pH 7.0) and NaCl at a final concentration of 0.5M, and the cells were disrupted by sonication. After centrifugation at 12000rpm for 20 minutes, the centrifuged supernatant was applied to a Ni-NTA nickel column (QIAGEN) for purification, and then eluted with 10mM Tris-HCl (pH 7.0) (containing 0.5M sodium chloride) containing 50mM imidazole, 250mM imidazole and 500mM imidazole, respectively, to collect protein peaks, followed by electrophoresis for further use.

Example 215 establishment of E11D5E11 hybridoma cell line

Immunization

The Inhibin-alpha protein fusion protein obtained in example 1 was mixed and emulsified with an equal volume of complete Freund's adjuvant (CFA, Sigma) and 18-20g of Balb/c mice (purchased from Wu's laboratory animal, Fuzhou) were immunized by abdominal injection at a dose of 50. mu.g/mouse. Thereafter, the booster was administered every 14 days, and the antigen was emulsified with Freund's incomplete adjuvant (IFA, Sigma Co.) at a dose of 25. mu.g/mouse. The polyclonal titer of the anti-immunogen in the serum of the mice is detected by indirect ELISA (wavelength 450nm) 14 days after the 2 nd boosting immunization, the mice with the highest titer are injected by tail vein for impact immunization, and the antigen is uniformly mixed by PBS solution with the dosage of 50 mu g/mouse.

Secondly, cell fusion:

aseptically preparing mouse spleen cell suspension with qualified immunity, mixing with mouse myeloma cell sp2/0(ATCC) at a ratio of 5:1, centrifuging at 1000rpm for 10min, discarding supernatant, adding 1mL of PEG (Sigma) solution preheated to 37 ℃ from slow to fast within 1 min, and slightly rotating the centrifuge tube during the addition process to make the cells fully contact with PEG. Standing at room temperature for 90s, adding 4mL serum-free DMEM (Hyclone company) medium preheated to 37 deg.C from slow to fast within 2min, adding 10mL preheated serum-free DMEM medium within 2min, adding the rest preheated serum-free DMEM medium within 2min,the volume is fixed to 50mL, the centrifuge tube needs to be slowly shaken in the whole adding process, the uniform mixing is ensured, and the damage to cells is reduced. Standing at room temperature for 10min, centrifuging (1000rpm, 5min), discarding supernatant, resuspending cells in 10-20mLHAT (Sigma) medium, and diluting with HAT medium to final concentration of 0.5X 10⁶cells/mL, all solutions were transferred to 96-well plates at 200. mu.L/well and labeled. The 96-well plates were carefully transferred to 37 ℃ with 5% CO₂Culturing in an incubator. The growth state and potential pollution of cells are regularly checked, and the incubator is opened and closed as little as possible to ensure the stability of the culture environment. On day 5 post-fusion, plates were supplemented with HAT medium at 50. mu.L/well.

Thirdly, cloning and ELISA screening positive hybridoma cells:

when the fused cell diameter is about 1-2mm, 50-200. mu.L of culture supernatant is aspirated for the first cell selection (ELISA, IHC-P and other methods of detection), and HAT medium is added to the culture wells to 200. mu.L. And (3) detecting the culture solution supernatant by ELISA, transferring all cell culture solution in the culture hole with the positive result obtained by detection to a 24-hole culture plate, supplementing HT medium, culturing for 3 days at a concentration of 2 mL/hole.

And repeatedly screening each cell line in the 24-pore plate, and removing the culture well cells which are not positive results to obtain the culture well cells with better positive results. Performing subclone screening on the positive well cells obtained from the 24-well culture plate by limiting dilution method, namely adding cell sap obtained by limiting dilution method into 96-well culture plate, and transferring to CO₂Culturing in an incubator for 11 days, and repeating cell screening when the diameter of the cloned cell is 1-2 mm. According to the detection result, 4 well-grown monoclonal positive culture wells are selected from each subcloned cell line, and transferred to a 24-well plate for continuous culture. After a period of time, a positive clone cell line obtained by cloning in a 24-well plate is screened again, namely a hybridoma cell line 15E11D5E11 secreting a specific monoclonal antibody. The cell line is transferred into a T-75 culture flask to be amplified to a logarithmic growth phase for seed preservation or subsequent experiments are carried out.

EXAMPLE 3 preparation of monoclonal antibodies by in vitro culture

First, in vitro culture

After obtaining the stable hybridoma cell line, obtaining the monoclonal antibody by adopting an in vitro culture method.

The hybridoma cells were cultured in DMEM complete medium containing 10% fetal bovine serum, and then centrifuged at low speed to collect culture supernatant, which was stored at 4 ℃ for further use.

Secondly, purification of monoclonal antibody

Antibody purification using rProtein A sepharose Fast Flow (GE) affinity column: filling a proper amount of purchased ProteinA filler into a gravity chromatographic column, and washing the gravity chromatographic column with an equilibrium buffer solution (a 0.1M Tris solution containing 1.5MNacl, pH7.0) until the equilibrium is reached; secondly, loading, namely adding cell supernatant filtered by a 0.22-micron filter membrane into a packed chromatographic column, and controlling the flow rate to be 1 drop/second; thirdly, balancing, and washing the sample solution to be balanced by using a balancing buffer solution after the sample solution is loaded; eluting, adding an elution buffer solution (0.1M citric acid solution, pH4.5) to wash the column and collecting the eluent; fifthly, regenerating, adding an equilibrium buffer solution to wash the column to be balanced after the elution is finished, washing the column with 2 times of column volume of 20 percent ethanol, and storing the column at 4 ℃. And finally, identifying the purity of the antibody by adopting an SDS-PAGE method. The result is shown in figure 1, the polyacrylamide gel electrophoresis picture of the purified Inhibin-alpha monoclonal antibody has the purity of more than 95 percent, and the concentration of the antibody is measured by an ultraviolet micro-spectrophotometer method and reaches more than 3.0 mg/mL.

EXAMPLE 4 characterization of monoclonal antibodies

Identification of one, two subtypes

The antigen protein was diluted to 1. mu.g/mL coated ELISA plates, 100. mu.L per well, coated overnight at 4 ℃, the liquid was decanted, the plates were washed 3 times with PBS (PBS-T) containing 0.05% Tween, 200. mu.L of blocking solution (PBS-T solution containing 2% BSA) was added per well, and incubated for 1h at 37 ℃. The liquid was decanted and washed 3 times with PBS-T. 0.1mL of culture supernatant of hybridoma cell line diluted 5-fold was added to each well and incubated at 37 ℃ for 1 hour. The liquid was decanted and washed 3 times with PBS-T. Using a confining liquid 1: HRP-labeled goat anti-mouse (kappa, lambda, IgM, IgG1, IgG2a, IgG2b, IgG) diluted 400₃IgA) antibody (Southern Biotech) was added in an amount of 0.1mL per well and incubated at 37 ℃ for 1 hour. The liquid was decanted and washed 3 times with PBS-T. 100 μ L of substrate (A, B volume of mixed solution) per well (Hill Bio-technology Ltd.) was used for visualizationAnd (3) carrying out color reaction for 15min at room temperature, adding 50 mu L of 1N HCl solution into each hole to stop color reaction, and then measuring the OD value at the wavelength of 450nm by using a microplate reader. The results show that the monoclonal antibody of the present invention is a murine monoclonal antibody of the IgG1 type.

Second, determination of affinity constant

Inhibin-alpha protein was coated at 100. mu.g/ml, 100. mu.l/well, coated overnight at 4 ℃ and washed 3 times with PBS-T. Add 200. mu.l of blocking solution to each well and block for 1h at 37 ℃ and wash 3 times with PBS-T. The monoclonal antibody purified in example 4 was diluted to the following concentrations (unit: ng/mL): 2000. 500, 125, 62.5, 31.25, 15.625, 3.125, 0.625, incubation at 37 ℃ for 1h, PBS-T wash 3 times. HRP-labeled goat anti-mouse secondary antibody 1: diluted at 5000, 100. mu.l/well, incubated at 37 ℃ for 1h, and washed 3 times with PBS-T. Mu.l of TMB (Hiroshi, England Biotech Co., Ltd., Huzhou) color developing solution was added to each well, and the reaction was stopped by adding 100. mu.l of 1.0N hydrochloric acid solution for color development for 13 min. And measuring the light absorption value with the wavelength of 450nm by using a microplate reader. The OD values were plotted against the antibody dilution factor to find 1/2 the antibody concentration a corresponding to the "plateau OD value". The affinity constant was calculated to be 6.93X 10 using the following formula⁹。

III, monoclonal antibody reaction specificity and application effect

Selecting immunogen solution, detecting the recognition specificity of the monoclonal antibody of the invention by an immunoblotting method, and carrying out 15% polyacrylamide gel electrophoresis on Inhibin-alpha protein. The gel proteins were transferred to PVDF membrane by conventional wet transfer method. The membrane was placed in a 5% BSA-TBST solution (protein side down) and shaker blocked at 37 ℃ for 1h to eliminate non-specific background. After the blocking is finished, washing off 5% BSA-TBST by using TBST, adding the monoclonal antibody of Inhibin-alpha prepared by the invention, and shaking and incubating for 1h in a decoloring shaking table. After washing the membrane with TBST, the secondary antibody was added and incubated for 1h in a decolorizing shaker to allow the secondary antibody to bind fully to the primary antibody. The membrane was washed again with TBST and ECL color development kit was added. The experimental results are shown in FIG. 2, the immunoblotting of the Inhibin-alpha monoclonal antibody to detect human Inhibin-alpha protein: the band is single and darker, which indicates that the specific reaction between the antibody and the antigen is obvious.

Example 5 tissue chip staining and characterization

First, preparation of tissue wax block

HE section staining was performed on the sample tissue to determine the tumor lesion site. And (5) circling the lesion site and preparing to punch. When the receptor wax block is manufactured, a plastic frame is placed on a mold, melted paraffin (the melting point is 56-58 ℃) is poured into the mold, the tissue block is placed into wax liquid in the mold, then a proper amount of wax liquid is added to enable the tissue block to be completely embedded in the wax liquid, the mold is placed into a refrigerator with the temperature of-20 ℃ for 6min after being cooled to the room temperature, the wax block is taken out of the mold, and the section is sliced or placed into the refrigerator with the temperature of 4 ℃ for storage. After trimming, continuous slicing is carried out, the thickness is determined to be 4 mu m, the continuous slicing is rinsed in 40% alcohol, the slices are naturally unfolded, then the separated slices are transferred to warm water at 45 ℃ for 30 seconds, a glass slide treated by 2% APES acetone solution is used for mounting the slices, the prepared tissue chip is placed into an oven at 60 ℃ for baking for 2 hours, the slices are taken out for cooling at room temperature, and the tissue chip is placed into a refrigerator at-4 ℃ for storage.

Second, IHC staining and analysis

Conventional xylene dewaxing was performed 3 times for 6 minutes each time with 100%, 95%, 85% gradient ethanol hydration for 3 minutes each time and finally tap water rinse. Antigen retrieval was performed and the sections were then placed in a wet box and washed 3 x 3min with PBS. Dropwise adding 3% H₂O₂Incubate for 10min and wash with PBS for 3 × 3 min. The PBS was spun off and the peroxidase blocker was added dropwise and incubated for 10 minutes at room temperature. Spin-drying the slices, dripping primary antibody diluted in a proper proportion (the dilution proportion of the antibody is designed according to the concentration of the antibody in the primary dilution) and incubating for 1 hour at room temperature (25 ℃), washing for 3X 3 minutes by PBS, dripping secondary antibody and incubating for 30 minutes at room temperature, washing for 3X 3 minutes by PBS, throwing off the PBS, and developing for 3-10 minutes by using a freshly prepared DAB developing solution. Hematoxylin counterstain for 20 seconds, PBS turns blue. Dehydration was carried out in a gradient of 85% (3 min), 95% (3 min), 100% (3 min) and 100% (3 min) in order, and finally two times xylene was cleared for 10min, followed by sealing with neutral gum.

The immunohistochemical staining results were divided into: positive and negative. Positive expression must be at a specific antigenic site in cells and tissues to be considered positive. Under the condition that the tissue staining distribution is clear and the cell positioning is accurate, the staining result is further divided according to the difference of staining intensity, which is as follows:

1. the sample is weakly positive; marked "+";

2. the sample is moderately positive; marked "+";

3. the sample is highly positive; marked as "+ + +".

4. The sample was negative and marked "-".

Thirdly, sample detection results:

the results of the detection of the anti-Inhibin-alpha protein monoclonal antibody (15E11D5E11) prepared by the invention in 21 cases of mesothelioma, 25 cases of ovarian interstitial tumor and 1 case of adrenocortical adenoma are shown in the following table:

the results show that the staining of the anti-Inhibin-alpha protein monoclonal antibody (15E11D5E11) is accurate in localization, clear in staining, free of non-specific staining and clean in background, which indicates that the anti-Inhibin-alpha protein monoclonal antibody (15E11D5E11) is strong in specificity. FIG. 3 is a graph showing immunohistochemical staining results for ovarian solitary stromal tumors.

Finally, it should be noted that, although the above embodiments have been described in the text and drawings of the present application, the scope of the patent protection of the present application is not limited thereby. All technical solutions which are generated by replacing or modifying the equivalent structure or the equivalent flow according to the contents described in the text and the drawings of the present application, and which are directly or indirectly implemented in other related technical fields, are included in the scope of protection of the present application.

SEQUENCE LISTING

<110> Fuzhou mai New Biotechnology development Co., Ltd

<120> anti-Inhibin-alpha protein monoclonal antibody, cell line, preparation method and application thereof

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Claims

1. The monoclonal antibody for resisting Inhibin-alpha protein is characterized in that the amino acid sequences of heavy chain and light chain variable regions of the monoclonal antibody are respectively the amino acid sequences shown in SEQ ID NO.2 and SEQ ID NO. 3.

2. The monoclonal antibody of claim 1, wherein the heavy and light chain variable region amino acid sequences of the monoclonal antibody are encoded by the nucleotide sequences set forth in SEQ ID No.4 and SEQ ID No.5, respectively.

3. The monoclonal antibody of claim 1, wherein the antigen used for immunizing a mouse in the preparation process of the monoclonal antibody is a recombinant protein encoded by the nucleotide sequence shown in SEQ ID No.1 and recombinantly expressed by Escherichia coli.

4. The monoclonal antibody of claim 1, which specifically recognizes human Inhibin- α protein.

5. The monoclonal antibody of claim 1, which is produced by a hybridoma cell line having a collection number of CGMCC No. 22320.

6. The monoclonal antibody of claim 1, wherein said anti-Inhibin- α protein is a mouse IgG1 subtype monoclonal antibody.

7. The method for preparing the monoclonal antibody against Inhibin-alpha protein as claimed in any of claims 1 to 6, wherein the antigen used for immunizing the mouse is a recombinant protein encoded by the nucleotide sequence shown in SEQ ID NO.1 and recombinantly expressed in Escherichia coli.

8. A hybridoma cell line for secreting an anti-Inhibin-alpha protein monoclonal antibody, wherein the cell line is a mouse hybridoma cell line 15E11D5E11, and the cell line is preserved in the China general microbiological culture Collection center with the preservation number: CGMCC NO. 22320.

9. Use of the anti-Inhibin- α protein monoclonal antibody of any of claims 1-6 in human Inhibin- α protein immunoassay.

10. An immunoassay reagent for human Inhibin-alpha protein, characterized in that the immunoassay reagent contains the anti-Inhibin-alpha protein monoclonal antibody of any one of claims 1 to 6 as an active ingredient.