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Mycoplasma Hyopneumoniae (MHP) Mycoplasma Test Kit Antibody ELISA 96 Wells/Kit

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Shenzhen Wensidun Technology Co., Ltd.

Mycoplasma Hyopneumoniae (MHP) Mycoplasma Test Kit Antibody ELISA 96 Wells/Kit

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Product Details

Mycoplasma Hyopneumoniae (MHP) Antibody ELISA Kit 96 Wells/Kit

 

1. Usage


The Mycoplasma hyopneumoniae (MHP) Antibody ELISA test kit is used for the detection of the MHP antibody in swine serum; assessment the immunity conditions against MHP virus, serological diagnosis of pig infection in the pig farms and investigation of the epidemiology of the MHP virus.


2. Principle


This kit use indirect ELISA method, MHP antigen is pre-coated on enzyme micro-well strips. When testing, add diluted serum sample, after incubation, if there is MHP specific antibody, it will combine with the pre-coated antigen, discard the uncombined antibody and other components with washing; then add enzyme labled anti-MHP antibody, combine with the antigen-antibody complex on the plate; discard the uncombined enzyme conjugate with washing; Add TMB substrate in micro-wells, blue product formed enzymatically, after adding stop solution to stop the reaction, use ELISA reader at 450nm wavelength to measure the absorbance A value in reaction wells.


3. The kit components

 

CodeItemSpec.CodeItemSpec.
1

MHP-AgCoatedplates

96 wells

1/2 plates7Negativecontrol2 ml
2EnzymeConjugate11/22 ml8Positive control1.6 ml
310X Concentrated washing buffer100 ml9Serum dilution plate1/2 pieces
4Substrate11/22 ml10Adhesive Foil2/4 pieces
5Sample diluent100 ml11Instruction sheet1 piece
6Stop solution15 ml   

 

4. Materials Required But Not Provided


1) Micropipettors: 0.5μL~10μL,10μL~100μL,100μL~1000μL
2) Disposable pipette tips
3) Measuring cylinder: 500 ml
4) 96 wells microplate reader
5) Distilled water or deionied water
6) Bottle or microplate washing machine


5. Samplepreparation


Take animal whole blood, get serum by using regular method, the serum should bright and no hemolysis.


6. Washing buffer preparation


Return 10X Concentrated washing buffer into room temperature before use, if there is salt crystals, shake to make it dissolved, then dilute it at 10 times with distilled water or deionized water. The diluted washing buffer can store at 4℃for about 1 week.


7. Sample dilution


At serum dilution plate, dilute serum at 1:100 with sample diluent.
Notice: Negative control and Positive control do not need dilute. Exchange tip after taking sample every time, record the situation of the sample on plate accurately. Shake the sample evenly before adding it.


8. Notes


1) All reagents should be adjusted to the room temperature and shake evenly before using, store at 2-8 ℃after using
2) Do not exchange the reagents from the kits of different lot numbers to use. Avoid reagent pollution when using.
3) Substrate and stop solution may have excitant to skin and eyes, pay attention when using.
4) Do not expose TMB (Substrate) to light and avoid it contact with antioxidants.
5) The wells should avoid damp or touching water after unsealing (Put the un-using microtiter strips back to bag with dehydrator in 2~8 ℃soon )
6) Deal all waste reasonable before dumping to avoid pollution.
7) Strictly adhere to instruction to get best result. All procedure including pipetting, timing and washing etc. must be accurate.
8) Serum dilution plate is disposable, do not use for second time; the MAX volume of it is 300μL/well.


9. TestProcedure


1) Take pre-coated microtiter strips (Can unseal for several time use as per sample quantity), add 100μL diluted serum to test well, meanwhile set 1 well for Negative control, 2 wells for Positive control separately. Add 100 μL Negative/Positive control to its well. Shake gently, do not overflow.
2) Cover andincubate at 37℃ for 30 min.
3) Pour the liquid out of the wells, add 250 μL diluted washing solution to each well, pour out. Repeat 4-6 times, at last pat to dry on absorbent paper.
4) Add 100 μL Enzyme Conjugate to each well, cover andincubate at 37℃ for 30 min.
5) Repeat the step 3(washing). Remember pat to dry on absorbent paper at last.
6) Add 100 μL substrate to each well, mix properly, cover andreact for 10 min at 37℃ at dark.
7) Add 50 μL stop solution in each well, and measure the result within 10 min.


10. Results


Read the OD value with ELISA reader at 450nm(630nm as reference)
For the assay to be valid:
OD Value of Negative control (N)< 0.2, meanwhile average OD value of Positive control (P)>0.4.
Calculation method:
Sample OD value / Positive control OD Average value= S/P value
The result is judged by S/P value:
If S/P≥0.5, it is positive; If S/P< 0.5, it is negative.


Expiry date:12 months.
Storage:Store at 2~8℃, in the dark.
Production Date:On outer-packing of the test kit.

 

 

 

 

 

 

 

Q1: How long will it take for you to ship?
A1: Usually ships within 7 working days.

 

Q2: Do you support OEM/ODM?
A2: can be supported. We can customize according to your specific needs and specific quantities.

 

Q3: How is your factory doing in terms of quality control?
A3: We have ISO9001 certification and ISO13485 certification, so far all the production process, we have standard rules, we comply with the relevant behavior and laws of the government.

 

Q4: Is after-sales service guaranteed?
A4: We provide professional online technical after-sales service. If the product fails during the experiment, we can provide
one-to-one guidance through telephone, video and other forms.

 

Q5: What is your minimum order quantity?
A5: 1Kit.

 

Q6: What is the shipping method?
A6: Usually by air, we will choose the best shipping method for you, and we can also ship according to the shipping method you require.

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