CN109810191A - A kind of anti-ovine skeletal muscle Troponin I monoclonal antibody and its application - Google Patents
A kind of anti-ovine skeletal muscle Troponin I monoclonal antibody and its application Download PDFInfo
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- CN109810191A CN109810191A CN201811625597.3A CN201811625597A CN109810191A CN 109810191 A CN109810191 A CN 109810191A CN 201811625597 A CN201811625597 A CN 201811625597A CN 109810191 A CN109810191 A CN 109810191A
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Abstract
The present invention relates to a kind of anti-ovine skeletal muscle Troponin I monoclonal antibody and its applications, belong to immunological technique field and Food Safety Analysis technical field.The anti-monoclonal antibody is secreted by the hybridoma cell strain that deposit number is CCTCC NO:C2018218 to be generated, which is 1:2.56 × 105, hypotype IgM, affinity constant Ka=7.6 × 108L/mol.The monoclonal antibody can be used for preparing the enzyme linked immunological kit of ovine skeletal muscle Troponin I and colloidal gold examination chromatograph test strip in detection fresh meat and its product, to achieve the purpose that quick and delicately mutton derived component detection in detection animal derived food.
Description
Technical field
The present invention relates to a kind of anti-ovine skeletal muscle Troponin I monoclonal antibody, generate the hybridoma of the monoclonal antibody
The application of cell strain and the antibody on detection ovine skeletal muscle Troponin I, belongs to immunological technique field and food safety
Analysis technical field.
Background technique
In meat product, due to price, religion, health etc., it is true that many countries formulate laws and regulations requirement food labelling
It is real clearly to mark meat sources, forbid adulterated behavior, to protect the interests of consumer, but obscures meat kind in the market
Phenomenon is still very universal, and adulterated mode includes the means such as mixing, being mixed into, extracting, palming off, especially with beef or mutton product
Doping, adulterated behavior are most commonly seen, these adulterated behaviors greatly compromise the interests of consumer.
Currently, many laboratories all use the derived component in Protocols in Molecular Biology means detection meat products both at home and abroad,
DNA detection method means multiplicity, predominantly nucleic acid probe hybridization, DNA fingerprint analysis, PCR specific amplified, PCR-RFLP etc..This
A little methods have certain sensitivity, however, there are also it is at high cost, height, heavy workload, Bu Nengxian are required to test object
, there is very big uncertainty in the disadvantages of field detecting especially for cooked meat product detection, because this is largely dependent upon cold cuts
The treatment process of product, the diversity of production process result in the different Degradation Levels of genetic stew.Furthermore this method can only be examined
Survey the possibility source of animal DNA, it is necessary to the moment prevents cross contamination, milk, blood, fat be likely to be DNA source.Cause
This, needs other methods mutually to confirm come its testing result with him.Immunological method have high sensitivity, specificity it is good,
The features such as at low cost, easy to operate, is suitable for batch samples and screens, and wherein enzyme linked immunosorbent assay and colloidal gold strip are most
Common method.
However cooked meat product will generally pass through high temperature, HIGH PRESSURE TREATMENT, many albumen are all become in this process
Property, antigenicity and water solubility are lost, this just brings difficulty to the foundation of immunological method.To Immunological Method is applied to
The detection of animal derived materials, it is necessary to find a specific heat-staple protein as marker antigen, then develop
Out for the monoclonal antibody of the specificity of this antigen.Troponin I (TnI) in animals skeletal muscle has kind specificity,
It can be used as a kind of heat-resisting type marker protein, distinguish the meat type source of different genera life, cooked meat product.With ovine skeletal muscle flesh
Calcium protein I (skTnI) is target detection thing, is able to achieve the foundation of mutton derived component immunology detection authentication technique.Therefore, resist
The preparation of ovine skeletal muscle Troponin I monoclonal antibody has the immunological test identification work for carrying out mutton meat derived components
Important practical significance and social effect.
Summary of the invention
The technical problem to be solved by the present invention is to overcome existing meat source property detection technique defect, a kind of anti-sheep bone bone is provided
Flesh Troponin I monoclonal antibody, the monoclonal antibody have specificity, the anti-monoclonal to ovine skeletal muscle Troponin I
Antibody is generated by the hybridoma cell strain skTnI-3D3 that deposit number is CCTCC NO:C2018218.Further, the present invention will
The monoclonal antibody is applied to detection ovine skeletal muscle Troponin I.
Technical problem of the present invention is realized by the following technical solutions.
A kind of anti-ovine skeletal muscle Troponin I monoclonal antibody, the monoclonal antibody are CCTCC NO by deposit number:
The hybridoma cell strain of C2018218 generates.The hybridoma cell strain is named as hybridoma cell strain skTnI-3D3, in 2018
On December 20, in delivers China typical culture collection center (CCTCC) preservation.
Above-mentioned anti-ovine skeletal muscle Troponin I monoclonal antibody can be specifically bound with ovine skeletal muscle Troponin I, potency
For 1:2.56 × 105, hypotype IgM, affinity constant Ka=7.6 × 108L/mol。
Above-mentioned ovine skeletal muscle Troponin I monoclonal antibody is for preparing the sheep bone bone in detection fresh meat and meat products
Application in the non-diagnostic purpose testing product of flesh Troponin I.
Above-mentioned application, the non-diagnostic purpose testing product are enzyme-linked immunologic detecting kit or colloid gold chromatographic test paper
Item.
Further, a kind of enzyme linked immunological kit detecting ovine skeletal muscle Troponin I, containing described in the kit
Anti- ovine skeletal muscle Troponin I monoclonal antibody.
A kind of colloid gold chromatographic test paper strip detecting ovine skeletal muscle Troponin I, the anti-sheep is contained in the test strips
The monoclonal antibody of skeletal troponin I.
A method of above-mentioned ovine skeletal muscle Troponin I monoclonal antibody is prepared, is included the following steps:
(1) preparation of antigen
Take sheep skeletal muscle remove fat and connective tissue, be ground, weigh 40g be added 0.15M NaCL solution (1:
2w/v)；After further mixing, ultrasonic extraction 5min (50W, 20KHz), then with after boiling water heating 20min, 2000g is centrifuged
30min；Removal precipitating takes after half supernatant liquid filtering as treatment fluid 1.The other half supernatant 121 DEG C of high pressures 30min, 5000g
After being centrifuged 30min, with Whatman No. 1 filter paper filtering, 90% ethyl alcohol (1:3.74v/v) is added in filtrate, take mixed liquor 7000g from
Heart 20min is treatment fluid 2 after taking 37 DEG C of drying of precipitating, physiological saline to redissolve.Treatment fluid 1 and treatment fluid 2 are through SDS-PAGE electrophoresis
After identification, skTnI electrophoretic band is ground, with after normal saline dilution respectively as detection antigen and immunizing antigen.
(2) ovine skeletal muscle Troponin I monoclonal antibody is prepared:
(a) animal immune: the female Balb/c mouse of 6-8 week old is immunized in the immunizing antigen of selective extraction, and interval is exempted from for 2 weeks
Epidemic disease 1 time, 3 times it is immune after docking take hematometry potency and inhibiting rate, select the optimal mouse of immune result to prepare fusion；
(b) cell fusion: the splenocyte and mouse myeloma SP2/0 cell for the mouse for taking step (a) selected are merged,
Indirect elisa method measures supernatant and chooses positive high hole, is subcloned by limiting dilution assay to positive hole, until establishing
Generate the hybridoma cell strain of the monoclonal antibody of single anti-ovine skeletal muscle Troponin I；
(c) a large amount of preparations of monoclonal antibody: choosing the biggish female Balb/c mouse of individual, induces ascites using internal
Method largely prepares ascites, and purifies ascites by octanoic acid-ammonium sulfate precipitation, is divided into tubule, and -20 DEG C of preservations obtain ovine skeletal muscle
Troponin I monoclonal antibody.
A method of it identifying above-mentioned ovine skeletal muscle Troponin I monoclonal antibody characteristic, includes the following steps:
(a) titration
Will test antigen diluent with the carbonate buffer solution of pH9.6 is that 5 μ g/ml are coated with detection plate, by Dan Ke after purification
Grand antibody carries out 1:2000, and 1:4000,1:8000 ... ... 1:1024000 dilution are added in ELISA Plate hole, are added after reaction
The sheep anti mouse secondary antibody of HRP label, is finally developed the color with TMB, the results show that ovine skeletal muscle Troponin I monoclonal after purification is anti-
Potency when bulk concentration is 1mg/mL reaches 1:2.56 × 105。
(b) hypotype measures
Hypotype measurement is carried out using the mouse source monoclonal antibody hypotype identification kit purchased from Sigma company, the results show that sheep bone bone
Flesh Troponin I monoclonal antibody hypotype is IgM.
(c) affinity determination
It is affine as the result is shown using the affinity costant of indirect elisa method measurement ovine skeletal muscle Troponin I monoclonal antibody
Constant Ka=7.6 × 108L/mol。
(d) specific assay
With the cross reaction of indirect ELISA measurement monoclonal antibody and the skeletal muscle extract of sheep, ox, chicken, duck, pig.Knot
Fruit shows that the potency of sheep skTnI-3D3 and ruminant (sheep, sheep) skeletal muscle extract is 1:100 ten thousand, with chicken, duck, pig bone bone
The potency of flesh extract is lower than 1:1 ten thousand, and specificity is preferably.
Monoclonal antibody provided by the invention can be applied to ovine skeletal muscle Troponin I in test sample, mainly by it
Applied to the enzyme-linked immunologic detecting kit and colloid gold test strip paper for preparing the detection of ovine skeletal muscle Troponin I.The present invention provides
The quality of anti-ovine skeletal muscle Troponin I monoclonal antibody there is very strong controllability and repeatability, and as to obtained by
The preliminary analysis and identification of antibody characteristic provide reality for the further foundation and application of special, sensitive method of immunity
Test foundation.
Detailed description of the invention
Fig. 1 extraction ovine skeletal muscle Troponin I SDS-PAGE qualification figure of the present invention, Fig. 1 a cromogram, Fig. 1 b black and white
Figure
Fig. 2 ovine skeletal muscle Troponin I antibody titer measurement chart of the present invention
Fig. 3 ovine skeletal muscle Troponin I monoclonal antibody hypotype measurement chart of the present invention
Fig. 4 ovine skeletal muscle Troponin I monoclonal antibody specificity measurement chart of the present invention
The hybridoma cell strain skTnI-3D3 of anti-ovine skeletal muscle Troponin I monoclonal antibody of the present invention, in
Deliver China typical culture collection center (abbreviation CCTCC, address: Wuhan University, Chinese Typical Representative culture on December 20th, 2018
Object collection, postcode: 430072) preservation, deposit number CCTCC NO:C2018218.
Specific embodiment
Invention is further described in detail With reference to embodiment, and cited embodiment is not to the present invention
Content and protection scope constitute any restrictions.
The materials, reagents and the like used in the following examples is commercially available unless otherwise specified.
The preparation of the ovine skeletal muscle Troponin I antigen of the present invention of embodiment one
Take sheep skeletal muscle remove fat and connective tissue, be ground, weigh 40g be added 0.15M NaCL solution (1:
2w/v)；After further mixing, ultrasonic extraction 5min (50W, 20KHz), then with after boiling water heating 20min, 2000g is centrifuged
30min；Removal precipitating takes after half supernatant liquid filtering as treatment fluid 1.The other half supernatant 121 DEG C of high pressures 30min, 5000g
After being centrifuged 30min, with Whatman No. 1 filter paper filtering, 90% ethyl alcohol (1:3.74v/v) is added in filtrate, take mixed liquor 7000g from
Heart 20min is treatment fluid 2 after taking 37 DEG C of drying of precipitating, physiological saline to redissolve.Treatment fluid 1 and treatment fluid 2 are through SDS-PAGE electrophoresis
After identification, qualification result is shown in Fig. 1, the results showed that, treatment fluid 1 and treatment fluid 2 have protein band in 21~22kD, with document report
21~24kD of molecular weight of skTnI be consistent.SkTnI electrophoretic band is ground, with after normal saline dilution respectively as detection
Antigen and immunizing antigen.
The preparation of the ovine skeletal muscle Troponin I monoclonal antibody of the present invention of embodiment two
(1) animal immune: the female Balb/c mouse of 6-8 week old being immunized with the immunizing antigen of preparation, is spaced 2 weeks immune 1
Secondary, immune process is shown in Table 1, three exempt from after docking take hematometry potency and inhibiting rate, select the optimal mouse of immune result to prepare to melt
It closes；
Flow chart is immunized in table 1
(2) cell fusion: fusion mouse plucks eyeball bloodletting, using serum as positive control, takes off aseptic condition after neck is put to death
Lower taking-up spleen, prepares splenocyte, is merged in the ratio of 5:1 by PEG with SP2/0 cell, fused cell suspension is added
96 orifice plates for entering to be covered with feeder cells, are put into 37 DEG C, 5%CO2Incubator in cultivate；
(3) screening of positive hybridoma cell strain: fused cell, next day check for polluting, the 10th day after fusion
Use HT culture medium instead.It changes after liquid 2-3d and carries out positive hole screening with indirect ELISA, pick out strong positive, single clone, thin as far as possible
The good hole of born of the same parents' state, is subcloned by limiting dilution assay, while being expanded culture, being frozen, until establishing single secretion
The monoclonal cell strain of antibody.
(4) a large amount of preparations of monoclonal antibody: using the method for inducing ascites in Mice Body, the Balb/c female of health is taken
Mouse adjusts cloning positive hybridoma cell 10 after every mouse internal injection paraffin oil 0.5mL, 7d6/ mL, every mouse
1mL is injected intraperitoneally, takes within 7-9 days ascites, fat is abandoned in centrifugation, is purified through octanoic acid-ammonium sulfate, and -20 DEG C of preservations after freeze-drying obtain sheep bone
Bone flesh Troponin I monoclonal antibody.
The ovine skeletal muscle Troponin I monoclonal antibody CHARACTERISTICS IDENTIFICATION of the present invention of embodiment three
(1) titration uses indirect elisa method, the specific steps are as follows:
Coating: being coated with carbonate buffer solution dilution as far as concentration is 5 μ g/mL, 96 hole elisa Plates, 100 hole μ L/, 4 DEG C of mistakes
Night；
Washing: coating plate restores to room temperature, and coating buffer of inclining, every hole adds 300 μ L of washing lotion, stands l min, washing 3 every time
It is secondary, it pats dry for the last time；
Closing: every hole adds washing lotion of the 200 μ L containing 10% calf serum, 37 DEG C of 1h；Incline deblocking liquid, washs 3 times, pats dry；
Add primary antibody: monoclonal antibody being started into doubling dilution with 1:2000 times with washing lotion, 100 μ L are added in every hole, and blank pair is arranged
According to hole (PBS) and negative control (negative serum), 37 DEG C of placement 45min；Incline primary antibody, washs 3 times, pats dry；
Add ELIAS secondary antibody: the mountain sheep anti-mouse igg of the diluted HRP enzyme label of l:10000 times of 100 μ L of every hole addition, 37 DEG C
Place 30min；Incline secondary antibody, washs 3 times, pats dry；Colour developing: every hole adds 100 μ L of substrate developing solution, and 37 DEG C are protected from light 15min；
Terminate: 50 μ L terminate liquids are added in every hole, terminate reaction；
Detection: measurement wavelength is the absorbance value (A450nm) at 450nm.
Result judgement: (A sample well-A blank control)/(A negative control-A blank control)≤2.1, and negative control
A450nm less than 0.2 when, the extension rate of antibody is antibody titer at this time.As a result see Fig. 2, anti-ovine skeletal muscle troponin
Potency when I monoclonal antibody 3D3 concentration is 1mg/ml reaches 1:2.56 × 105。
(2) hypotype measures
Hypotype measurement is carried out using the mouse source monoclonal antibody hypotype identification kit purchased from Sigma company.Hybridoma secretion
The secondary antibody colour developings of monoclonal antibody and different subclass have notable difference, wherein the A450nm value highest with Ig M secondary antibody, with Ig
The secondary antibody colour developing of G1 is faint, and hardly develops the color with Ig G2a, Ig G2b, Ig G3 and Ig A secondary antibody, as a result as shown in figure 3,
The Antibody types of 3D3 secretion are based on IgM.
(3) affinity determination
Affinity costant (Ka) is measured using non-competing ELISA method.Specific step is as follows:
Coating: being coated with carbonate buffer solution dilution as far as concentration is 1,0.5,0.1,0.05 μ g/mL, 96 hole elisa Plates
100 holes μ L/ are coated with respectively, and 4 DEG C overnight；Incline coating buffer, washs 3 times, pat dry；
Closing: every hole adds washing lotion of the 200 μ L containing 10% calf serum, 37 DEG C of 1h；Incline deblocking liquid, washs 3 times, pats dry；
Add monoclonal antibody: monoclonal antibody being started into doubling dilution with 100 μ g/mL with washing lotion, 100 μ L, 37 DEG C of heat and moisture preservings are added in every hole
45min；Incline primary antibody, washs 3 times, pats dry；
Add ELIAS secondary antibody: the mountain sheep anti-mouse igg of the l:10000 times of diluted HRP enzyme label of every hole addition 100uL, 37 DEG C
Place 30min；Incline secondary antibody, washs 3 times, pats dry；
Colour developing: every hole adds 100 μ L of substrate developing solution, and 37 DEG C are protected from light 15min；
Terminate: 50 μ L terminate liquids are added in every hole, terminate reaction；
Detection: measurement wavelength is the absorbance value (A450nm) at 450nm.Ka is calculated according to the following formula
Ka=(n-1)/2 (n Ab '-Ab)
In formula: Ab is antigen concentration when being Ag, generates the antibody concentration of half absorbance value；Ab ' is that antigen concentration is Ag '
When, generate the antibody concentration of half absorbance value；Extension rate of the n between Ag and Ag ' is surveyed using non-competing enzyme-linked immunization
Determine the affinity costant of antibody, after measured ovine skeletal muscle Troponin I monoclonal antibody affinity costant Ka=7.6 × 108L/mol。
(4) specific assay
Using indirect competitive ELISA method, the specific steps are as follows:
Coating: extremely with carbonate buffer solution dilution coating antigen (sheep, sheep, chicken, duck, Animal muscles Troponin I extract)
Concentration is 5 μ g/mL, and 96 hole elisa Plates, 100 hole μ L/, 4 DEG C overnight；Incline coating buffer, washs 3 times, pat dry；
Closing: every hole adds washing lotion of the 200 μ L containing 10% calf serum, 37 DEG C of 1h；Incline deblocking liquid, washs 3 times, pats dry；
Add primary antibody: monoclonal antibody being started into doubling dilution with 1:2000 times with washing lotion, 100 μ L are added in every hole, and blank pair is arranged
According to hole (PBS) and negative control (negative serum), 37 DEG C of placement 45min；Incline primary antibody, washs 3 times, pats dry；
Add ELIAS secondary antibody: the mountain sheep anti-mouse igg of the diluted HRP enzyme label of l:10000 times of 100 μ L of every hole addition, 37 DEG C
Place 30min；Incline secondary antibody, washs 3 times, pats dry；
Colour developing: every hole adds 100 μ L of substrate developing solution, and 37 DEG C are protected from light 15min；
Terminate: 50 μ L terminate liquids are added in every hole, terminate reaction；
Detection: measurement wavelength is the absorbance value (A450nm) at 450nm.
Result judgement: (A sample well-A blank control)/(A negative control-A blank control)≤2.1, and negative control
A450nm less than 0.2 when, the extension rate of antibody is antibody titer at this time.As a result see Fig. 4, sheep skTnI-3D3 with ruminate
Animal sheep, ovine skeletal muscle extract potency 1:25 ten thousand, be lower than 1:1 ten thousand with the potency of chicken, duck, Animal muscles extract, specifically
The application of the preferable example IV ovine skeletal muscle Troponin I monoclonal antibody of the present invention of property
The present embodiment is that ovine skeletal muscle Troponin I monoclonal antibody of the present invention is establishing detection ovine skeletal muscle troponin
The enzyme-linked immunologic detecting kit or the applicating example after colloid gold chromatographic test paper strip method of I, can be used for fresh meat and its system
The detection of ovine skeletal muscle Troponin I in product.
(1) sample pre-treatments
Fresh meat removal fat and connective tissue, meat processing food remove casing, and the NaCL for weighing 1g addition 0.15M is molten
Liquid 2ml (1:2w/v), heats 20min with boiling water after homogenate, and 2000g is centrifuged 30min；Removal precipitating, supernatant is with Whatman 1
Filter paper filtering collects filtrate for detecting.
(2) antibody is detected applied to enzyme-linked immunologic detecting kit method
The testing principle of kit is double crush syndrome method in the present invention.It is coated with microplate with antibody (3D3),
Solid-phase capture antibody is made, sequentially adds standard items or sample into the micropore of coating monoclonal antibody, then with horseradish peroxidase mark
The detection antibody (3A8) of note combines, and forms antibody-antigene-hrp-antibody complex, TMB is added to develop the color, blue, in the work of acid
With lower finally in yellow, shade is positively correlated with bovine muscle Troponin I content in sample.
Detection: ovine skeletal muscle Troponin I monoclonal antibody does 1:1000 dilution, 100 holes μ L/, 4 DEG C of coatings with carbonate buffer solution
Overnight；Washing, pats dry；It is closed with the PBS containing 1% gelatin, 200 holes μ L/, 37 DEG C of incubation 2h；Washing, pats dry；Be added to
Sample product, 37 DEG C of incubation 1h；Washing, pats dry；It is added the ox skTnI-3A8 monoclonal antibody of diluted HRP label, 100 holes μ L/, 37 DEG C
Incubate 1h；Washing, pats dry；100 hole μ L/ of developing solution is added, develop the color 15min, and 50 hole μ L/ of terminate liquid, measurement is then added.
Result judgement:
(a) quantitative analysis: calculating separately the mean absorbance values of standard items and sample to be tested, standard items or sample to be tested
Absorbance value (B) is ordinate, and the logarithm of normal concentration is abscissa, draws standard curve；By the absorbance value of sample to be tested
Standard curve is substituted into, corresponding concentration can be found out, be the content of sample multiplied by extension rate.
(b) it qualitative analysis: is compared with the mean absorbance values of sample to be tested with the absorbance value of standard items, you can get it
The concentration range of sample to be tested.
(3) antibody is detected applied to colloid gold chromatographic test paper strip method
Reaction principle carries out qualitative detection, sheep present in sample to ovine skeletal muscle Troponin I using double-antibody method
Skeletal troponin I is first in conjunction with the antibody of gold particle label during moving up along test strips, forms golden labelled antibody-sheep
Skeletal troponin I compound, the ovine skeletal muscle Troponin I captured in antibody and compound being fixed on NC film carry out
In conjunction with the colour developing of T location (detection line) is strong and weak directly proportional to the content of ovine skeletal muscle Troponin I in sample.
Detection: taking out ovine skeletal muscle Troponin I colloid gold chromatographic test paper strip, and sample end is inserted into analyte sample fluid,
Insertion depth is no more than mark line, and about 10-20 seconds taking-up test strip is horizontally arranged, and observation in 3-5 minutes determines detection knot
Fruit, result is invalid after 10 minutes.
Result judgement: one reddish brown colo(u)r streak of corresponding quality control region location of C (nature controlling line) display on coated film, detection zone T
It sets and does not show reddish brown colo(u)r streak, indicate that testing result is feminine gender, illustrate in sample to be tested without containing ovine skeletal muscle Troponin I；
T, location of C show two reddish brown colo(u)r streaks on coated film, indicate that result is the positive, illustrate in sample to be tested containing ovine skeletal muscle
Troponin I；Test paper whether quality control region C does not show brownish red band, then no matter detection zone T shows brownish red band
It is invalid to be judged to.
The technical concept and advantage of above-described embodiment only to illustrate the invention, the present invention also can have other forms and become
Change, as well known to the skilled person, above-described embodiment is functioned only as to the exemplary role in foregoing invention protection scope, right
For those of ordinary skill in the art, there are also many conventional deformations and other implementations in the protection scope defined by the present invention
Example, these deformations and embodiment all will be within the pending protection scopes of the present invention.
Claims (7)
1. a kind of anti-ovine skeletal muscle Troponin I monoclonal antibody, which is characterized in that the monoclonal antibody is by deposit number
The hybridoma cell strain skTnI-3D3 of CCTCC NO:C2018218 is generated.
2. anti-ovine skeletal muscle Troponin I monoclonal antibody according to claim 1, which is characterized in that the antibody titer
For 1:2.56 × 105, hypotype IgM, affinity constant Ka=7.6 × 108L/mol。
3. a kind of hybridoma cell strain for generating anti-ovine skeletal muscle Troponin I monoclonal antibody as claimed in claim 1 or 2
SkTnI-3D3, which is characterized in that it is preserved in China typical culture collection center, deposit number CCTCC NO:
C2018218, the deposit date is on December 20th, 2018.
4. anti-ovine skeletal muscle Troponin I monoclonal antibody as claimed in claim 1 or 2 is for preparing detection biological sample
In ovine skeletal muscle protein I non-diagnostic purpose testing product in application.
5. application according to claim 4, which is characterized in that the non-diagnostic purpose testing product is ELISA reagent
Box or colloid gold chromatographic test paper strip.
6. a kind of enzyme linked immunological kit for detecting ovine skeletal muscle Troponin I, which is characterized in that containing as weighed in the kit
Benefit require 1 or 2 described in anti-ovine skeletal muscle Troponin I monoclonal antibody.
7. a kind of colloid gold chromatographic test paper strip for detecting ovine skeletal muscle Troponin I, which is characterized in that containing such as in the test strips
The monoclonal antibody of anti-ovine skeletal muscle Troponin I of any of claims 1 or 2.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109709338A (en) * | 2018-12-28 | 2019-05-03 | 河北省科学院生物研究所 | Detect ox or the enzyme linked immunological kit of ovine skeletal muscle Troponin I and the preparation method and application thereof |
| CN109709339A (en) * | 2018-12-28 | 2019-05-03 | 河北省科学院生物研究所 | Detect colloidal gold immuno-chromatography test paper strip and the application of ox or ovine skeletal muscle Troponin I |
| CN113402608A (en) * | 2021-06-24 | 2021-09-17 | 河北省科学院生物研究所 | Hybridoma cell strain, monoclonal antibody secreted by hybridoma cell strain and application of monoclonal antibody |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN109709338A (en) * | 2018-12-28 | 2019-05-03 | 河北省科学院生物研究所 | Detect ox or the enzyme linked immunological kit of ovine skeletal muscle Troponin I and the preparation method and application thereof |
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| CN109709339B (en) * | 2018-12-28 | 2022-03-15 | 河北省科学院生物研究所 | Colloidal gold immunochromatographic test strip for detecting skeletal muscle troponin I of cattle or sheep and application thereof |
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| CN113402608A (en) * | 2021-06-24 | 2021-09-17 | 河北省科学院生物研究所 | Hybridoma cell strain, monoclonal antibody secreted by hybridoma cell strain and application of monoclonal antibody |
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