HBeAg ELISA Kit (Elisa equipment)

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Quick Details
Pathological Analysis Equipments
Brand Name:
Place of Origin:
Jiangsu, China
Shelf Time:
2 years
Packaging & Delivery
Packaging Details
Shanghai port
Lead Time :
after payment within 30days


Elisa equipment
1.easy to use
2.easy to read
3.High accuracy
4.High speed


Elisa equipment



Product Description

This HBeAg ELISA is a qualitative enzyme immunoassay for the in vitro detection of Hepatitis B E Antigen (HBeAg)
in human serum or plasma. It is intended to use in medical laboratories for diagnosis and management of patients
related to infection with hepatitis B virus.
1. Microplate           96 wells
2. Negative Control         1 mL ×1
3. Positive Control         1 mL ×1
4. Conjugate           6 mL ×1
5. Washing Buffer (20×)        20 mL ×1
6. Substrate Solution A         6 mL ×1
7. Substrate Solution B         6 mL ×1
8. Stop Solution          6 mL ×1
9. Plate Cover          2 pieces
10. Insert            1 copy 


1. Prepare Reagents: Dilute 1 volume of Concentrated Washing Buffer  (20×)with 19 volumes of distilled water,
mix well.
2. Add Samples and Conjugate: Open the foil pouch and remove the Microplate. Set up 1 well as Blank, 2 wells
as negative control, 2 wells as positive control. After dispensing 50µL Samples and 50µL Negative Control or
Positive Control to the respective wells, add 50μl of Conjugate into each well except the blank. Gently
vibrating the plate. 
3. Incubate: Cover the Microplate with Plate Cover  and incubate the Microplate in a thermostat-controlled
water-bath or microplate incubator at 37°C for 30 minutes.
4. Wash the Plate: Remove the plate cover. Aspirate the contents of all wells. Fill the wells with the diluted
washing buffer ( 10~20 seconds to soak) then aspirate again. Repeat the procedure for 5 times. Make sure
that the rest volume is minimal, by tapping plate onto absorbent paper.
5. Add Substrate: Add 50µL of Substrate Solution A and 50µL of Substrate Solution B to each well, mix well.
Cover and incubate at 37°C for 10 minutes.
6. Stop reaction: Add 50µL Stop Solution to each well, mix well.
7. Read the absorbance at 450 nm. If a dual wavelength measurement is used, the reference wavelength should
be selected from 620nm to 690nm.





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