CN108845138A - ELISA kit based on IgM antibody detection food allergen - Google Patents
ELISA kit based on IgM antibody detection food allergen Download PDFInfo
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- CN108845138A CN108845138A CN201810413987.8A CN201810413987A CN108845138A CN 108845138 A CN108845138 A CN 108845138A CN 201810413987 A CN201810413987 A CN 201810413987A CN 108845138 A CN108845138 A CN 108845138A
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6854—Immunoglobulins
Abstract
ELISA kit provided by the invention based on IgM antibody detection food allergen, belongs to food allergen detection technique field.The kit includes following reagent, is coated with the detection plate of food allergen；Washing buffer；Sample diluting liquid；Standard items or positive quality control product；The anti-human IgM antibodies of biotin labeling；The avidin solution of enzyme label；Substrate developing solution；Terminate liquid.The characteristics of present invention selects IgM for the first time to detect food allergen, and is the ELISA kit based on indirect method preparation, has detection sensitivity strong, and accuracy is high, favorable reproducibility, and being capable of the large batch of sample of single treatment.Embodiment proves that kit detection sensitivity provided by the invention reaches 10ng/ml.
Description
Technical field
The present invention relates to food allergen detection technique fields, and in particular to based on IgM antibody detection food allergen
Kit, i.e. food allergen specificity IgM detection kit.
Background technique
Anaphylactia disease incidence accounts for 30% of total world population or more, is classified as the four big of 21 century by the World Health Organization
One of noninfectious disease.The disease incidence of anaphylactia significantly rises in recent years, becomes the public health problem of global concern,
Guo Jia et al. is to anaphylactia epidemiological survey the results show that there is 22% people to suffer from anaphylaxis disease in 1,200,000,000 total populations
Disease, such as allergic rhinitis, asthma, conjunctivitis, eczema, food hypersenstivity, drug allergy and serious allergic reaction etc., serious shadow
Ring people's lives quality and life security.
Food allergen such as egg product, peanut, milk, soya bean, wheat, tree nuts, fish and crust group food, are main
Food allergen.Wherein in crust group food, shrimp allergen is concerned, it was reported that 0.6%~2.8% anaphylactia is suffered from
Person's prawn allergy；People detect at least 13 kinds of IgE binding proteins in shrimp, but tropomyosin is accredited as only master
Anaphylactogen is wanted, relative molecular mass is between 34000~39000；It is reported that tropomyosin is shrimp, crab, oyster, cuttlefish
The important antigen of equal invertebrates, has highly conserved amino acid sequence.In egg allergy, albumen is easier to cause than yolk
Allergy, ovomucoid are main allergen；Its positive rate is up to 35% in children's food hypersenstivity, and adult allergy is also up to
12%.Due to the seriousness and frequently-occurring of peanut allergy reaction, which causes the extensive concern of medical institutions, it was reported that food
In the allergic reaction of object induction, peanut allergy accounts for 10%~47%.Such disease is increasing in recent years, becomes common disease, more
Morbidity is China's health and the significant problem that economic development field needs to solve.
Currently, patent CN1620504A is disclosed with based on the information design obtained by a part of gene of predetermined substance
Primer carries out PCR, for measuring the method in food whether there is or not predetermined substance, micro constitutent and identification contained in detection food
It is excellent in terms of harmful predetermined substance anaphylactogen, but this method relies on the primer of known detectable substance, but PCR method is multiple
Miscellaneous, detection time is long, at high cost；Patent CN101285840A discloses a kind of detection method of anaphylactogen in food, although should
Method can quickly and easily obtain testing result but not disclose relevant detection antibody type hypotype in the patent, not have simultaneously
There are the detection sensitivity and accuracy of open this method detection food allergen.In addition, with the molecular weight peaks and figure of flight mass spectrum
Spectral shape is the protein site that basic parameter carrys out identification mark.By the feature of diagnosis allergy original albumen to anaphylactogen in food into
Row Testing and appraisal, but need special large-scale precision instrument, testing cost is high, analyze it is difficult need special testing staff and
Analysis personnel
Although all there is detection speed in conclusion there are many method for the related food allergen detection studied at present
Slowly, at high cost, the problem of being not suitable for batch detection, and also it is machine-readable to need specific analysis instrument to carry out, and constrains mistake in food
The development of quick former detection.
Summary of the invention
In view of this, it is an object of the invention to the kit based on IgM detection food allergen there is the kit
Stronger specificity and higher sensitivity.
In order to achieve the above-mentioned object of the invention, the present invention provides following technical scheme：
The present invention provides the ELISA kits based on IgM antibody detection food allergen, including following components：
It is coated with the detection plate of food allergen；
Washing buffer；
Sample diluting liquid；
Standard items or positive quality control product；
The anti-human IgM antibodies of biotin labeling；
The avidin solution of enzyme label；
Substrate developing solution；
Terminate liquid.
Preferably, the peridium concentration of the food allergen is 0.1~2000 μ g/ml.
Preferably, the type for being coated with food allergen in the detection plate of food allergen includes aquatic products category, poultry
Birds, egg-milk, greengrocery, fruits, cereals or nut fruits.
Preferably, the washing buffer is PBS buffer solution.
Preferably, the mass concentration of the anti-human IgM antibodies of the biotin labeling is 0.01~8000 μ g/ml.
Preferably, the substrate developing solution is tetramethyl benzidine substrates solution or 2, and 2- hydrazine-bis- -3- ethyl is stupid and thiophene
Oxazoline -6- sulfonic acid substrate solution.
Preferably, the sample diluting liquid is PBS buffer solution.
Preferably, the PBS buffer solution comprises the following components in parts by weight：8.0 parts of NaCl, 0.20 part of KCl, 1.16 parts
Na2HPO4, 0.20 part of KH2PO4With 1000 parts of water；The pH value of the PBS buffer solution is 7.0~7.6.
Preferably, the hydrogen-oxygen that the sulfuric acid solution or mass concentration that the terminate liquid is 0.5~2mol/L are 30%~40%
Change sodium solution.
Preferably, the concentration of the avidin solution of the enzyme label is 1~5000 times of working solution when using.
ELISA kit provided by the invention based on IgM antibody detection food allergen, including following reagent, coating
There is the detection plate of food allergen；Washing buffer；Sample diluting liquid；Standard items or positive quality control product；Biotin labeling resists
Human IgM antibody；The avidin solution of enzyme label；Substrate developing solution；Terminate liquid.The present invention selects IgM to detect food allergen,
And the characteristics of ELISA kit prepared based on indirect method has detection sensitivity strong, and accuracy is high, favorable reproducibility, and energy
Enough large batch of samples of single treatment.Embodiment proves that kit detection sensitivity provided by the invention reaches 10ng/ml.
Further, it is provided by the invention based on IgM antibody detection food allergen ELISA kit, standard items or
Positive quality control product is people's IgM albumen, and food allergen albumen coated elisa plate can detecte oral in the liquid such as blood plasma, serum
The allergen specificity IgM that any food-induced body of feed generates, has the type of detection food allergen more, using model
Enclose wide feature.The sensitivity of testing result can be effectively improved using biotin-avidin system.
Detailed description of the invention
Fig. 1 is that kit of the present invention makes and uses flow chart；
Fig. 2 is the standard curve for the ELISA kit that IgM antibody detects food allergen in embodiment 1.
Specific embodiment
The present invention provides the ELISA kits based on IgM antibody detection food allergen, including following reagent：
It is coated with the detection plate of food allergen；
Washing buffer；
Sample diluting liquid；
Standard items or positive quality control product；
The anti-human IgM antibodies of biotin labeling；
The avidin solution of enzyme label；
Substrate developing solution；
Terminate liquid.
ELISA kit provided by the invention includes being coated with the detection plate of food allergen.The food allergen
Peridium concentration is preferably 0.1~2000 μ g/ml, more preferably 0.1~100 μ g/ml.It is described to be coated with food mistake in the present invention
The type of food allergen includes aquatic products category, fowl poultry kind, egg-milk, greengrocery, fruits, cereals in the detection plate of quick original
Or nut fruits.The aquatic products category includes fish, shrimp, crab, shellfish and clam etc..The fowl poultry kind includes pork, chicken, beef and sheep
Meat.Egg-milk includes egg and milk etc..The vegetables include radish, mushroom, celery, capsicum and green pepper.The fruits include
Citrus, orange, banana, apple, Kiwi berry, mango, grape, pineapple and tomato.The cereals include wheat, oat, rice,
Corn, soya bean and pea.The nut fruits include pine nut, peanut, fibert, walnut and American pistachios.
In the present invention, the type of the detection plate is preferably transparent polystyrene board and opaque white polyphenyl second
Alkene plate.The transparent polystyrene board is used for quantitative detection；The opaque white polystyrene plate is used for qualitative detection.
ELISA kit provided by the invention includes washing buffer.In the present invention, the washing buffer is preferably
PBS buffer solution.The solute of the PBS buffer solution preferably includes component 8.0 parts of NaCl, the 0.20 part of KCl of following parts by weight,
1.16 part Na2HPO4With 0.20 part of KH2PO4With 1000 parts of water；The pH value of the PBS solution is 7.0~7.6.
In the present invention, the ELISA kit includes sample diluting liquid.The sample diluting liquid is that pH value is 7.0~7.6
PBS buffer solution.The solute of the PBS buffer solution preferably includes component 8.0 parts of NaCl, the 0.20 part of KCl of following parts by weight,
1.16 part Na2HPO4, 0.20 part of KH2PO4With 1000 parts of water；The pH value of the PBS solution is 7.0~7.6.
ELISA kit provided by the invention includes the anti-human IgM antibodies of biotin labeling.The biotin labeling resists
The mass concentration of human IgM antibody is preferably 0.01~8000 μ g/ml.The addition body of the anti-human IgM antibodies of the biotin labeling
Product is preferably the hole 0.02~0.2ml/.In the present invention, the anti-human IgM antibodies are preferably the monoclonal antibody of anti-human IgM.
ELISA kit provided by the invention includes standard items or positive quality control product.The standard items or positive quality control product
For people IgM.The mass concentration of the positive quality control product is preferably 0.01~1000 μ g/ml；The additive amount of the positive quality control product
The hole preferably 0.02~0.2ml/.
ELISA kit provided by the invention includes enzyme label avidin solution.In the present invention, the enzyme marks Avidin
Solution is 1~5000 times of working solution when using.The present invention is not particularly limited the source of enzyme label Avidin, uses
Enzyme well-known to those skilled in the art marks avidin solution.
ELISA kit provided by the invention includes substrate developing solution.The substrate developing solution is tetramethyl benzidine bottom
Object solution or 2,2- hydrazine-bis- -3- ethyl is stupid and thiazoline -6- sulfonic acid substrate solution.The quality of the tetramethyl benzidine is dense
Degree preferably 0.02~0.05%；The 2,2- hydrazine-bis- -3- ethyl is stupid and the mass concentration of thiazoline -6- sulfonic acid is preferably
0.05~0.1mg/ml.
ELISA kit provided by the invention includes terminate liquid.The terminate liquid is preferably the sulfuric acid of 0.5~2.0mol/L
The sodium hydroxide solution that solution or mass concentration are 30%~40%, the more preferably sulfuric acid solution of 1.0mol/L or mass concentration
For 35% sodium hydroxide solution.
In the present invention, the preparation method of the ELISA kit based on IgM antibody detection food allergen, preferably
Preparation method including being coated with the detection plate of food allergen.
In the present invention, the preparation method of the detection plate for being coated with food allergen preferably includes following steps：
1) food allergen is diluted with coating buffer, obtains food allergen coating buffer；
2) the food allergen coating buffer that the step 1) obtains is added in the reacting hole of detection plate, 4 DEG C overnight；
3) next day adds confining liquid, washes again after incubation in step 2) described in once washing after overnight detection plate hole
It washs, obtains the detection plate for being coated with food allergen.
The present invention coating buffer dilution food allergen and people's IgM albumen, obtain coating buffer.It is described in the present invention
Diluted method is not particularly limited, using diluted technical solution well-known to those skilled in the art.In the present invention,
The coating buffer is preferably carbonate buffer solution.The concentration of the carbonate buffer solution is preferably 0.01~0.2mol/L.
The pH value of the carbonate buffer solution is preferably 8.5~9.5.
After obtaining coating buffer, the coating buffer is added in the reacting hole of detection plate by the present invention, and 4 DEG C overnight.The present invention
In, the volume of coating buffer is preferably the hole 0.02~0.2ml/ in each reacting hole.
In the present invention, described 4 DEG C preferably carry out under conditions of standing overnight, are coated on conducive to what food allergen consolidated
In detection plate.
Next day after overnight detection plate hole described in once washing, adds confining liquid, washs again after incubation.The present invention couple
There is no limit using the technical solution of washing well-known to those skilled in the art for the method for the once washing.This hair
In bright, the additive amount of the washing buffer is preferably at least the volume of coating buffer；The number of the once washing is preferably 2~
6 times；The incubation time of the single wash is preferably every time 0~5min (similarly hereinafter).
After the once washing, confining liquid is added in the detection plate after once washing by the present invention, is washed again after incubation.This
In invention, the confining liquid is preferably the balf serum albumin PBS buffer solution that mass concentration is 1%~5%.The confining liquid
Additive amount be preferably at least the volume of coating buffer.In the present invention, the time of the incubation is preferably 10~200min.It is described
The temperature of incubation is preferably 10~40 DEG C, and more preferably 15~35 DEG C.
After the incubation, the present invention will test plate and be washed again, in the present invention, the method washed again with
The method of once washing described in above-mentioned technical proposal is identical, and details are not described herein.
It is described wash again after, after the present invention preferably drains the moisture in detection plate naturally, with vacuum bag sealing detection plate,
Obtain the detection plate for being coated with food allergen.
In the present invention, the concentration of the anti-human IgM antibodies of the biotin labeling is preferably 0.01~8000 μ g/ml, more excellent
It is selected as 0.1~1000 μ g/ml, most preferably 0.1~100 μ g/ml.
The detection method of ELISA kit based on IgM antibody detection food allergen, includes the following steps：
1) sample to be tested is added in the detection plate hole for being coated with food allergen, PBS is added to coating someone IgM
In the detection plate hole of albumen, carry out carrying out first time washing after being once incubated for；
2) anti-human IgM antibodies of biotin labeling, secondary incubation are added in the detection plate into the step 1) after washing
It carries out washing for second afterwards；
3) avidin solution that enzyme marks or the strepto- that enzyme marks are added in the detection plate into the step 2) after washing
Avidin solution carries out third time washing after being incubated for three times；
4) to addition substrate developing solution in washing detection plate will be obtained in the step 3), after four times are incubated for, to detection plate
Middle addition terminate liquid, the detection plate to be developed the color；
5) the color developing detection plate obtained according to the step 4), obtains qualitative or quantitative result.
Sample to be tested is added in the detection plate for being coated with food allergen by the present invention, carries out for the first time after primary incubation
Washing.In the present invention, the sample to be tested includes the liquid containing IgM antibody such as serum, blood plasma.The addition of the sample to be tested
Amount is preferably the hole every 0.02~0.2ml/ of hole.The dilution of the liquid such as the serum or blood plasma is 1~32000 times.
In the present invention, in order to keep testing result accurately credible, blank control wells, negative control hole, standard are preferably also set up
Sample wells or positive quality control hole, and guarantee that the amount of liquid of each reacting hole addition is consistent.It is preferably carbonic acid in the blank control wells
PBS buffer solution is added as sample in the coated ELISA Plate hole of salt buffer；It is preferably food allergen in the negative control hole
The fluid samples such as serum or the blood plasma without allergies crowd are added in coated ELISA Plate hole；The standard sample wells or positive quality control
Hole, which is preferably used, is added PBS buffer solution as sample in the coated ELISA Plate hole of the carbonate buffer solution of the albumen of IgM containing people.
In the present invention, the temperature being once incubated for is preferably 10~40 DEG C, and more preferably 15~35 DEG C.It is described once to incubate
The time educated is preferably 10~200min.
In the present invention, the first time wash temperature is preferably 10~40 DEG C, and more preferably 15~35 DEG C；The washing is slow
The additive amount of fliud flushing is preferably at least the volume of coating buffer；The number of the once washing is preferably 2~6 times；The single is washed
The incubation time washed is preferably every time 0~5min (similarly hereinafter)
The anti-human IgM antibodies of biotin labeling are added into the detection plate after first time washing, secondary incubation is laggard
Second of washing of row.
In the present invention, the temperature of the secondary incubation is preferably 10~40 DEG C, and more preferably 15~35 DEG C.It is described secondary to incubate
The time educated is preferably 10~200min.
In the present invention, the method for second of washing is not particularly limited, and use is well-known to those skilled in the art
Washing methods.
After described second is washed, the avidin solution of enzyme label is added into the detection plate after the washing by the present invention,
Third time washing is carried out after being incubated for three times.
In the present invention, the avidin solution of enzyme label is diluted before use, and the diluted multiple preferably 1~
5000 times.In the present invention, the additive amount of the enzyme label avidin solution is preferably the hole 0.02~0.2ml/, more preferably
The hole 0.03~0.16ml/.
In the present invention, the temperature being incubated for three times is preferably 10~40 DEG C, and more preferably 15~35 DEG C.It is described to incubate three times
The time educated is preferably 10~200min.
In the present invention, the method for the third time washing is not particularly limited, and use is well-known to those skilled in the art
Washing methods.
After washing three times, substrate developing solution is added into obtained detection plate by the present invention, after four times are incubated for, into detection plate
Add terminate liquid, the detection plate to be developed the color.
In the present invention, the additive amount of the substrate developing solution is preferably the hole 0.02~0.2ml/, more preferably 0.03~
The hole 0.16ml/.
In the present invention, the temperature of four incubations is preferably 10~40 DEG C, and more preferably 15~35 DEG C.The incubation
Time is preferably 1~45min, more preferably 10~30min.
In the present invention, sulfuric acid solution or mass concentration 30% that the concentration of the terminate liquid is 0.5~2.0mol/L~
40% sodium hydroxide solution.The additive amount of the terminate liquid is preferably the hole 0.02~0.2ml/, more preferably 0.03~
The hole 0.16ml/.
The detection plate of the colour developing obtained described in observation or detection, obtains qualitative or quantitative result.
In the present invention, the qualitative results are colors in the reacting hole for observe by the naked eye detection plate, in blank well and yin
Property control wells do not develop the color, positive quality control hole develop the color in the case where, sample well colour developing is so judged as measuring samples for the positive；Instead
It, in the case where blank well and negative control hole do not develop the color the colour developing of positive quality control hole, sample well does not develop the color, then to be checked
Sample is feminine gender.
In the present invention, the quantitative result is judged by the OD value of solution in detection detection plate reacting hole, with blank
The OD value in each hole is surveyed after control wells zeroing, and carries out quantitative detection based on standard curve.It is described detection preferably when with
ABTS colour developing, then Detection wavelength is set as 405nm；When TMB colour developing, then Detection wavelength is set as 450nm.
In the present invention, standard curve is drawn using this field conventional scheme.Standard curve obtains straight line fitting equation:Y=A
+B×X；Wherein A=0.26718；B=0.00166；R2=0.99994.The ELISA reagent of IgM antibody detection food allergen
Box detection range is 10~1000ng/ml.
The kit provided by the invention based on IgM detection food allergen is carried out specifically below with reference to embodiment
It is bright, but they cannot be interpreted as limiting the scope of the present invention.
Embodiment 1
Coating：Egg white, wheat and milk foodstuff anaphylactogen are diluted to total protein mass concentration with carbonate buffer solution
For the food allergen coating buffer of 10 μ g/ml；Standard items coating buffer (albumen is obtained with carbonate buffer solution dilution people IgM albumen
1) concentration is shown in Table, 0.05ml coating buffer is separately added into each reacting hole of polystyrene board, 4 DEG C overnight.Next day discards in hole
0.35ml washing buffer is added in solution, every hole, washs 3 times, is incubated for 30s (referred to as washing, similarly hereinafter) every time；
Closing：PBS buffer solution (the closing containing 2% balf serum albumin of 0.05ml is separately added into each reacting hole
Liquid), pH：7.2,15~35 DEG C of incubation 120min, discard solution in hole, washing is same as above；
Sample is added：Suspicious egg, Wheat Dood Allergy patients serum and milk allergy patients serum (test serum), normal person
Serum (negative control hole) PBS buffer solution dilutes 100 times, and the serum after 0.05ml dilution is added in corresponding anaphylactogen in every hole
In coated ELISA Plate hole；Standard sample wells/positive quality control hole, the every hole of blank control wells are added 0.05ml PBS, and 15~35 DEG C
It is incubated for 60min, is washed out；
Add detection antibody：It is even that the biotin that the mass concentration of 0.05ml is 0.5 μ g/ml is added into each reacting hole by IgM
Anti-human IgM antibodies' solution of connection washs after 15~35 DEG C of incubation 60min；
The avidin solution of enzyme label：The Avidin that every hole is separately added into 0.05ml horseradish peroxidase-labeled is molten
Liquid, 15~35 DEG C of incubation 30min, is washed out；
Substrate solution is added to develop the color：Every hole is separately added into the tmb substrate solution 0.05ml of Fresh, and 15~35 DEG C are protected from light incubation
15min；
Terminate reaction：Every hole is separately added into 2mol/L sulfuric acid solution 0.05ml；
Detect OD value：ELISA Plate is placed in microplate reader, the absorbance value (OD at Detection wavelength 450nm450), with blank
The OD in each hole is surveyed after control wells zeroing450It is worth (table 1), and draws standard curve (attached drawing 2), food mistake is calculated according to standard curve
The concentration (table 2) of quick original specific IgM antibodies.The each Kong Jun of this experiment does multiple holes, and experiment is repeated 3 times.
1 human IgM antibody of table detects the standard concentration and its OD of the ELISA kit of food allergen450Value
| Serial number | People IgM protein concentration (ng/ml) | OD450It is worth (mean value) |
| 1 | 1000.0 | 1.9319 |
| 2 | 300.0 | 0.7743 |
| 3 | 100.0 | 0.4361 |
| 4 | 30.0 | 0.3228 |
| 5 | 10.0 | 0.2768 |
| 6 | 3.0 | 0.2454 |
| 7 | 1.0 | 0.2532 |
| 8 | 0 | 0.2569 |
Standard curve is drawn according to the OD Value Data of serial number 1,2,3,4,5 and 8 to be obtained directly such as attached drawing 2 according to standard curve
Line fit equation:Y=A+B × X；Wherein 0.26718；B=0.00166；R2=0.99994.It is available by embodiment 1：(1)
The ELISA kit detection range that IgM antibody detects food allergen is 10~1000ng/ml；(2) IgM antibody detects food
The sensitivity of the ELISA kit of anaphylactogen is 10ng/ml.
2 human IgM antibody of table detects the case where suspected allergies patients serum food allergen specificity IgM antibody
As seen from the above embodiment, the ELISA kit provided by the invention based on IgM antibody detection food allergen,
IgM is selected to detect food allergen, and the ELISA kit based on indirect method preparation, has detection sensitivity strong, accurately
The characteristics of degree is high, favorable reproducibility, and being capable of the large batch of sample of single treatment.Embodiment proves kit inspection provided by the invention
It surveys sensitivity and reaches 10ng/ml.Type with detection food allergen is more, the characteristics of having a wide range of application.
The above is only a preferred embodiment of the present invention, it is noted that for the ordinary skill people of the art
For member, various improvements and modifications may be made without departing from the principle of the present invention, these improvements and modifications are also answered
It is considered as protection scope of the present invention.
Claims (10)
1. the ELISA kit based on IgM antibody detection food allergen, which is characterized in that including following components：
It is coated with the detection plate of food allergen；
Washing buffer；
Sample diluting liquid；
Standard items or positive quality control product；
The anti-human IgM antibodies of biotin labeling；
The avidin solution of enzyme label；
Substrate developing solution；
Terminate liquid.
2. kit according to claim 1, which is characterized in that the peridium concentration of the food allergen be 0.1~
2000μg/ml。
3. kit according to claim 1, which is characterized in that described to be coated with food in the detection plate of food allergen
The type of anaphylactogen includes aquatic products category, fowl poultry kind, egg-milk, greengrocery, fruits, cereals or nut fruits.
4. kit according to claim 1, which is characterized in that the washing buffer is PBS buffer solution.
5. kit according to claim 1, which is characterized in that the quality of the anti-human IgM antibodies of the biotin labeling
Concentration is 0.1~2000 μ g/ml.
6. kit according to claim 1, which is characterized in that the substrate developing solution is that tetramethyl benzidine substrates are molten
Liquid or 2,2- hydrazine-bis- -3- ethyl is stupid and thiazoline -6- sulfonic acid substrate solution.
7. kit according to claim 1, which is characterized in that the sample diluting liquid is PBS buffer solution.
8. the kit according to claim 4 or 7, which is characterized in that the PBS buffer solution includes the group of following parts by weight
Point：8.0 parts of NaCl, 0.20 part of KCl, 1.16 parts of Na2HPO4, 0.20 part of KH2PO4With 1000 parts of water；The pH of the PBS buffer solution
Value is 7.0~7.6.
9. kit according to claim 1, which is characterized in that the terminate liquid is that the sulfuric acid of 0.5~2.0mol/L is molten
The sodium hydroxide solution that liquid or mass concentration are 30%~40%.
10. kit according to claim 1, which is characterized in that the concentration of the avidin solution of the enzyme label is to make
1~5000 times of used time working solution.
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| Application Number | Priority Date | Filing Date | Title |
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| CN201810413987.8A CN108845138A (en) | 2018-05-03 | 2018-05-03 | ELISA kit based on IgM antibody detection food allergen |
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| Application Number | Priority Date | Filing Date | Title |
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| CN201810413987.8A CN108845138A (en) | 2018-05-03 | 2018-05-03 | ELISA kit based on IgM antibody detection food allergen |
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Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009082798A1 (en) * | 2008-01-02 | 2009-07-09 | Fundação De Amparo À Pesquisa Do Estado De Minas Gerais - Fapemig | Method and kit for quantifying of allergen-especific human igg subclasses for the control and attendance of specific immunotherapy |
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2018
- 2018-05-03 CN CN201810413987.8A patent/CN108845138A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009082798A1 (en) * | 2008-01-02 | 2009-07-09 | Fundação De Amparo À Pesquisa Do Estado De Minas Gerais - Fapemig | Method and kit for quantifying of allergen-especific human igg subclasses for the control and attendance of specific immunotherapy |
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| Title |
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| ARISTO VOJDANI: "Detection of IgE,IgG,IgA and IgM antibodies against raw and processed food antigens", 《NUTRITION & METABOLISM》 * |
| J.H.FINE ET AL: "Immunomodulation by Gastrointestinal Carbon Black Nanoparticle Exposure in Ovalbumin T Cell Receptor Transgenic Mice", 《NANOTOXICOLOGY》 * |
| PATRICIA MACCHIAVERNI: "Early Exposure to Respiratory Allergens by Placental Transfer and Breastfeeding", 《PLOS ONE》 * |
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