null

Bird Flu (H9N1) Antibody Elisa Test Kit | LSY-30018

(No reviews yet) Write a Review
SKU:
767-LSY-30018
Method:
Elisa
Size:
96 Wells/kit
Species:
Poultry
Specimen:
Serum
€377.00
Frequently bought together:

Description

Green Spring Bird Flu (H9N1) Antibody Elisa Test Kit - LSY-30018 from Shenzhen Lvshiyuan Biotechnology Co.,Ltd.

Bird Flu subtype H9 antibody ELISA test kit   

Catalog No. LSY-30018

1. Usage

This kit is used to detect Bird Flu subtype H9 antibody in chicken serum, to assess antibody condition by Bird Flu subtype H9 vaccine in chicken farm and assist diagnosis of serological infected chicken.

2. Principle

The Bird Flu subtype H9 antibody ELISA kit is based on an indirect enzymatic immunoassay (Indirect ELISA).The antigen is coated on plates. When a sample serum contains specific antibodies against virus, they will bind to the antigen on plates. Wash the unbound antibodies and other components. Then add a specific enzyme conjugate. After incubation and washing, add the TMB substrate. A colorimetric reaction will appear, measured by a spectrophotometer (450 nm).

3. Reagents

1

H9 antigen coated microplate

1/2 plate of 96 wells

7

Negative control 

0.8/1.6ml

2

Enzyme conjugate 

11/22 ml

8

Positivecontrol

0.8/1.6ml

3

10×concentrated washing buffer

100ml

9

Serum dilution plate

1/2 piece

4

Substrate solution

11/22 ml

10

Adhesive film

2/4 pieces

5

Sample dilution

100ml

11

Instruction

1 piece

6

Stopping solution

11/22ml

12

 

 

4.Materials required but not provided

1) Micropipettors and disposable tips: 0.5μL~10μL、10μL~100μL、100μL~1000μL

2) 37 ℃ Incubator

3) 96 wells microplate reader

4) Distilled water or deionied water

5) Bottle or microplate washing machine 

5. Sample preparation

Take animal whole blood, make serum according to regular methods, the serum should be clear, have no hemolysis.

6. Preparation of washing buffer

Return washing solution to room temperature before use, if there is salty crystals, shake to make the crystals dissolve, then use distilled water or deionized water to dilute it at 10 times. The diluted washing solution can store for 1 week at 4 ℃.

7. Sample dilution

At serum dilution plate, dilute serum at 1:100 with sample dilution (for example: 495μL sample dilution + 5μL serum)

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 B) to light and avoid it contact with antioxidants.

5) The wells should avoid damp or touching water after unsealing (Put the un-using microplate 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. ELISA procedure

1) Take pre-coated microplate (Can unseal for several time use as per sample quantity), add 100μL diluted serum to sample wells, meanwhile set 1 well for Negative control, 2 wells for Positive control separately. Add 100 μL Negative/Positive control to its wells. Shake softly (do not spill), cover and incubate at 37℃ for 30 min.

2) Pour the liquid out of the wells, add 250μL diluted washing solution to each well, pour out. Repeat 5 times, then pat to dry on absorbent paper.

3) Add 100 μL Enzyme Conjugate to each well, cover andincubate at 37℃ for 30 min.

4) Repeat the step 2(washing). Remember pat to dry on absorbent paper at last.

5) Add 100μL substrate solution to each well, mix properly,react for 10 min at 37℃ in dark.

6) Add 50 μL stop solution in each well, and measure the result within 10 min.

10. Results

Read the OD value with microplate-reader at 450nm (630nm as reference).

For the test to be valid:

OD value of Negative control (N) < 0.15, meanwhile OD value of Positive control (P)〉0.4.

Calculation method:

OD value of samples/ Average OD value of Positive control = S/P value

Result judge:

S/P≥0.25, Positive.

S/P < 0.25, Negative;

Specifications: 96 or 96*2 wells/kit.

Expiry date:12 months.

Storage: Storing at 2-8℃, in the dark.

View AllClose

0 Reviews

View AllClose