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Hepatitis E virus IgG antibody diagnostic kit
(Enzyme-linked immunosorbent assay) Manual
[Name]:Hepatitis E virus IgG antibody diagnostic kit (enzyme-linked immunosorbent assay)
[Generic name:The hepatitis E virus IgG antibody diagnostic kit (enzyme-linked immunosorbent assay)
[Name]:
[Name]:Anti-HEV IgG ELISA Kit
[Packaging specifications:The 96 people were / box; 48 people were / box;
[Expected] uses:qualitative detection in human serum or plasma hepatitis E virus IgG antibody
Principle [test]
The kit used genetic engineering recombinant expression of high-grade,high-activity HEV virus-specific antigen (ORF2,ORF3) coated ELISA plates,horseradish peroxidase (HRP) labeled anti-mouse IgG (r chain) Monoclonal antibody tracer,TMB color system,indirect ELISA for detection in human serum or plasma in the hepatitis E virus IgG antibodies,applicable to the diagnosis of hepatitis E and hepatitis E virus infection of the epidemiological investigation.
[Kit comprising:
Kit packaging specifications 96T/48T
1,measured by the HEV-IgG-board 96-/ 48 -
2,on a diluted specimen bottles (12 ml/6ml)
3,of a combination of bottles (12 ml/6ml)
4,washing liquid (20 x) 1 bottle (50 ml/25ml)
5,a bottle of liquid substrate (6 ml/3ml)
6,the termination of a bottle (6 ml/3ml)
7,a bottle of negative control (0.5 ml/0.3ml)
8,a bottle of positive control (0.5 ml/0.3ml)
9,in a statement
10,a Plastic Bag
11,formwork two closures
[Specimen collection and preservation]
By conventional methods serum samples collected from the vein.Plasma samples can be conventional dosage of anticoagulant heparin or sodium citrate.Determination within five days of the specimens can be placed in the preservation of -20 ℃ at least three months.Specimens avoid hemolysis or repeated freeze solution.Turbid or sediment samples should be clarified after centrifugation or filtration detection.The serum must be kept in the collection,preservation should pay attention to the process of aseptic operation.
[Steps]
1,for a blank hole,without any liquids (2 hole for each of the negative control,2 Kongyang of control).Diluted liquid samples from 100 μ l Add reaction hole,using sample of the 3rd Army blending more than 37 ℃ for 30 minutes.
2,washed with distilled water will be diluted by 20 times after plate washer.Abandoning a previous rejection reaction solution,in each hole by adding diluted washing liquid 300 μ l,still 30 seconds.Rejection of disposable washing liquid,so repeatedly washed five times,the last in the shoot dry absorbent paper.
3,each hole by adding enzyme conjugate 100 μ l,and 37 ℃ for 30 minutes.
4,plate washer five times,with two steps.
5,followed by adding at the end of each hole of A,B of the 50 μ l,37 ℃ dark color for 10 minutes.
6,the termination of each hole by adding 50 μ l,blending termination reaction.Determination within 30 minutes OD value.
[Results] found
Meibiaoyi a wavelength of 450.Stay in the gaps with air-conditioning,and then read the hole OD value.
Critical value (Cutoff) = 0.10 + average OD value of the negative control (negative control average OD value
1年前
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