Bovine α1 acid glycoprotein (α1-AGP) elisa kit instruction manual
Elisa kit specifications: 48-well configuration / 96-well configuration
Standard diluent: 1.5ml × 1 bottle
Enzyme label reagent: 3 ml × 1 bottle (48) / 6 ml × 1 bottle (96)
[Bovine α1 Acid Glycoprotein (α1-AGP) elisa kit] This reagent is for research use only
Calculation:
Taking the concentration of the standard as the abscissa and the OD value as the ordinate, draw a standard curve on the coordinate paper, and find the corresponding concentration from the standard curve according to the OD value of the sample; then multiply by the dilution factor; Calculate the linear regression equation of the standard curve with the OD value, substitute the OD value of the sample into the equation, calculate the sample concentration, and multiply it by the dilution factor to obtain the actual concentration of the sample.
Kit composition:
Sealing film: 2 pieces (48) / 2 pieces (96)
Instructions: 1 copy
Sealed bag: 1
Standard product: 2700ng / L 0.5ml × 1 bottle 0.5ml × 1 bottle Store at 2-8 ℃
Enzyme-coated plate: 1 × 48 1 × 96 2-8 ℃
Sample diluent: 3ml × 1 bottle 6ml × 1 bottle Store at 2-8 ℃
Developer A solution: 3ml × 1 bottle 6 ml × 1 bottle Store at 2-8 ℃
Developer B: 3ml × 1 bottle 6 ml × 1 bottle Store at 2-8 ℃
Stop solution: 3ml × 1 bottle 6ml × 1 bottle Store at 2-8 ℃
Concentrated washing solution: (20ml × 20 times) × 1 bottle (20ml × 30 times) × 1 bottle Store at 2-8 ℃
ã€Bovine α1 Acid Glycoprotein (α1-AGP) elisa kit】 Precautions:
1. The kit should be equilibrated at room temperature for 15-30 minutes before being taken out of the refrigerated environment. If the enzyme label coated plate is unopened, the strip should be stored in a sealed bag.
2. Crystals may be precipitated in the concentrated washing liquid, which can be heated and dissolved in a water bath during dilution, and the results will not be affected during washing.
3. The sampler should be used at each step of sample addition, and the accuracy should be regularly checked to avoid test errors. It is best to control the sampling time within 5 minutes. If there are many specimens, it is recommended to use a volley gun to add samples.
4. Please make a standard curve at the same time of each measurement, it is best to make a double hole. If the content of the test substance in the specimen is too high (the OD value of the sample is greater than the OD value of the first well of the standard well), please first dilute it with a certain multiple (n times) of the sample diluent and then determine it. When calculating, please multiply the total dilution Multiple (× n × 5).
5. The sealing film is limited to one-time use to avoid cross-contamination.
6. Please keep the substrate away from light.
7. Strictly follow the instructions, and the test results must be determined by the microplate reader.
8. All samples, washing liquids and various wastes should be treated as infectious agents.
9. The components of different batches of this reagent shall not be mixed.
10. If there is any difference with the English manual, the English manual shall prevail.
Kit performance:
1. The correlation coefficient R between the linear regression of the sample and the expected concentration is above 0.95.
2. The batch and approval shall be less than 9% and 11% respectively
examination range:
0.2IU / L-6IU / L
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