Antigen HP Analysis Reagent Rapid Detection Kit

Antigen HP Analysis Reagent Rapid Detection Kit

The complete ELISA kit contains the following components: (1) Solid phase carrier (immunosorbent) coated with antigen or antibody; (2) Enzyme-labeled antigen or antibody (conjugate); (3) Substrate of enzyme; (4) Negative control substance and positive control substance (in qualitative determination), reference standard substance and control serum (in quantitative determination); (5) Diluent of conjugate and specimen; (6) Washing solution. In plate ELISA, the commonly used diluent is phosphate buffered saline containing 0.05% Tween 20; (7) Enzyme reaction termination solution. The commonly used HRP reaction termination solution is sulfuric acid, and its concentration varies according to the added amount and the final volume of the colorimetric solution. In plate ELISA, 3mol/L is generally used.
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Description
Technical Parameters

DIRECTIONS FOR USE Allow the test, specimen, extraction buffer to equilibrate to room temperature (15-30°C)prior to testing. 1.Remove the test device from the sealed foil pouch and use it as soon as possible. Place the test device on a clean and level surface. Best results will be obtained if the assay is performed immediately after opening the foil pouch. 2. Take out the Extraction Tube. 3. Take out 1 bottle of Sample Extraction Buffer, remove the bottle cap, add all the extraction buffer into the extraction tube. 4.Place the sterilized swab specimen in the sample extraction buffer. Rotate the swab for approximately 10 seconds while pressing the head against the inside of the tube to release the antigen in the swab. 5.Remove the sterilized swab while squeezing the sterilized swab head against the inside of Buffer as you remove it to expel as much liquid as possible from the swab. Discard the sterilized swab in accordance with your biohazard waste disposal protocol. 6. Screw on and tighten the Nozzle with Filter onto the specimen collection tube, then shake the specimen collection tube vigorously to mix the specimen and the sample extraction buffer 7.Add 3 drops of the solution (approx.80ul) to each sample well and then start the timer. Read the result at 10~20 minutes. Don't interpret the result after 20 minutes

Specification

Antigen

Positive

Negative

Total



Positive

255

32

287


Negative

45

968

1013


Total

300

1000

1300


2 - 3

20210223101403beb2a041193d4e33981b89ff85c1b1f8

20210223101403eab28216a59745f79d148003f4813a58

20210223101410da008638d3b241a49fa59e8309f5734f

20210223101415d80a8fe993fc492fb30a1e62ca644bd0

20210223101423a7cb0bc2dc02489ca15dccdf6f4bae4e

20210223101425700201f374e044b6a69258b8eb151f99

   

    

    

    

    

    

    

    


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