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产品名称:瘦素(LEP)ELISA试剂盒瘦素(LEP)ELISA试剂盒
![]()  | 1.Add 100 μL of standard or sample to each well.  | 
![]()  | ![]() 2.Remove the liquid.  | 
![]()  | ![]() 3.Add 100 μL Biotinylated Detection Ab. Incubate 1 hour at 37℃.Aspirate and wash 3 times.  | 
![]()  | ![]() 4.Add 100 μL HRP Conjugate. Incubate 30 min at 37℃.Aspirate and wash 5 times.  | 
![]()  | ![]() 5.Add 90 μL of Substrate Reagent. Incubate for 15 min at 37℃.  | 
![]()  | ![]() 6.Add 50 μL of Stop Solution.  | 
![]()  | ![]() 7.Read the OD at 450 nm immediately. Calculation of the results.  | 

1.Add 100 μL of standard or sample to each well.


2.Remove the liquid.


3.Add 100 μL Biotinylated Detection Ab. Incubate 1 hour at 37℃.Aspirate and wash 3 times.


4.Add 100 μL HRP Conjugate. Incubate 30 min at 37℃.Aspirate and wash 5 times.


5.Add 90 μL of Substrate Reagent. Incubate for 15 min at 37℃.


6.Add 50 μL of Stop Solution.


7.Read the OD at 450 nm immediately. Calculation of the results.

1.Add 100 μL of standard or sample to each well.


1.Add 100 μL of standard or sample to each well.
1.Add 100 μL of standard or sample to each well.
1.Add 100 μL of standard or sample to each well.

2.Remove the liquid.



2.Remove the liquid.

2.Remove the liquid.
2.Remove the liquid.

3.Add 100 μL Biotinylated Detection Ab. Incubate 1 hour at 37℃.Aspirate and wash 3 times.



3.Add 100 μL Biotinylated Detection Ab. Incubate 1 hour at 37℃.Aspirate and wash 3 times.

3.Add 100 μL Biotinylated Detection Ab. Incubate 1 hour at 37℃.Aspirate and wash 3 times.
3.Add 100 μL Biotinylated Detection Ab. Incubate 1 hour at 37℃.Aspirate and wash 3 times.

4.Add 100 μL HRP Conjugate. Incubate 30 min at 37℃.Aspirate and wash 5 times.



4.Add 100 μL HRP Conjugate. Incubate 30 min at 37℃.Aspirate and wash 5 times.

4.Add 100 μL HRP Conjugate. Incubate 30 min at 37℃.Aspirate and wash 5 times.
4.Add 100 μL HRP Conjugate. Incubate 30 min at 37℃.Aspirate and wash 5 times.

5.Add 90 μL of Substrate Reagent. Incubate for 15 min at 37℃.



5.Add 90 μL of Substrate Reagent. Incubate for 15 min at 37℃.

5.Add 90 μL of Substrate Reagent. Incubate for 15 min at 37℃.
5.Add 90 μL of Substrate Reagent. Incubate for 15 min at 37℃.

6.Add 50 μL of Stop Solution.



6.Add 50 μL of Stop Solution.

6.Add 50 μL of Stop Solution.
6.Add 50 μL of Stop Solution.

7.Read the OD at 450 nm immediately. Calculation of the results.



7.Read the OD at 450 nm immediately. Calculation of the results.

7.Read the OD at 450 nm immediately. Calculation of the results.
7.Read the OD at 450 nm immediately. Calculation of the results.
