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Model Number: ELISA HBsAg Standard
Key Specifications/Special Features:
INSTRUCTIONS FOR USEHBsAg ELISAASSAY PROCEDURE1. 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 wellsas negative control, 2 wells as positive control. After dispensing 50L Samples and 50L Negative Control orPositive Control to the respective wells, add 50μl of Conjugate into each well except the blank . Gentlyvibrating the plate.3. Incubate: Cover the Microplate with Plate Cover and incubate the Microplate in a thermostat-controlledwater-bath or microplate incubator at 37℃ for 30 minutes.4. Wash the Plate: Remove the plate cover. Aspirate the contents of all wells. Fill the wells with the dilutedwashing buffer ( 10~20 seconds to soak) then aspirate again. Repeat the procedure for 5 times. Make surethat the rest volume is minimal, by tapping plate onto absorbent paper.5. Add Substrate: Add 50L of Substrate Solution A and 50L of Substrate Solution B to each well, mix well.Cover and incubate at 37℃ for 10 minutes.6. Stop reaction: Add 50L 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.
RESULTS
1. For the assay to be valid, the mean OD value of negative controls must be less than or equal to 0.1 and the
mean OD value of positive controls must be greater than or equal to 0.8.
2. Cut off value = 2.1 × NC
NC= the mean absorbance value for two negative controls
Important: If the NC is lower than 0.05, take it as 0.05.
3. OD value of the sample ≥ cut off value, it is positive for HBsAg.
OD value of the sample < cut off value, it is negative for HBsAg.
PRECAUTIONS
1. Allow all kit components to reach room temperature before use.
2. Follow the direction insert to control the reaction temperature and time strictly.
3. Do not mix components of different lot numbers to use.
4. The kit should be store at 2-8℃. Do not use kit components beyond their expiration date.
7. Read the absorbance at 450 nm. If a dual wavelength measurement is used, the reference wavelength should
be selected from 620nm to 690nm.
RESULTS
1. For the assay to be valid, the mean OD value of negative controls must be less than or equal to 0.1 and the
mean OD value of positive controls must be greater than or equal to 0.8.
2. Cut off value = 2.1 × NC
NC= the mean absorbance value for two negative controls
Important: If the NC is lower than 0.05, take it as 0.05.
3. OD value of the sample ≥ cut off value, it is positive for HBsAg.
OD value of the sample < cut off value, it is negative for HBsAg.
PRECAUTIONS
1. Allow all kit components to reach room temperature before use.
2. Follow the direction insert to control the reaction temperature and time strictly.
3. Do not mix components of different lot numbers to use.
4. The kit should be store at 2-8℃. Do not use kit components beyond their expiration date.
Shipping Information:
- FOB Port: Shanghai
- Lead Time: 20 - 25 days
Main Export Markets:
- Asia
- Australasia
- Central/South America
- Eastern Europe
- Mid East/Africa
- North America
- Western Europe