Reagent kit and use based on antigen-antibody reaction
An antigen-antibody and kit technology, which is applied in the direction of chemical reaction of materials for analysis, biological testing, and material analysis by observing the influence of chemical indicators The number of detectors is reduced, the detection time is reduced and the detection comparability is improved.
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example 1
[0015] Example 1, preparation of rapid screening kit for blood donors
[0016]The kit in this example can be used for rapid screening of blood donors. The production of the kit probe board is to mix the HBsAg-immunized rabbit anti-HBsAg, HCV fusion antigen, HIV fusion antigen, and syphilis fusion antigen according to the optimal concentration and ratio, and then coat it on a 96-well microtiter plate. Bovine serum albumin blocked and then dried. The labeling system of the kit is composed of markers and substrates (substrate chromogenic solutions A and B). The markers use antigens and antibodies that are different from the coated antigen antibody and paired with the coated antigen antibody: anti-HBsAg, HCV Fusion protein antigen of HIV1+2, syphilis antigen. These antigens and antibodies used in the labeling system are enzyme-labeled separately or mixed at a determined concentration and ratio, and then used for later use. The auxiliary parts of the kit in this example include ...
example 2
[0017] Example 2, the preparation example of blood transfusion chip kit
[0018] In this example, the preparation of the probe board of the kit uses the activated glass slide as the carrier, and the probes used include anti-HBsAg, HCV antigen, HIV1+2 antigen, syphilis antigen, HTLV1+2 antigen, manual spotting, each antigen Point 6 sample points with the determined optimal concentration, each sample point diameter is 200um. After spotting, the blank carrier surface was blocked with bovine serum albumin and dried. The labeling system of the kit in this example uses antigens and antibodies that are different from the original coated antigen antibody paired with the coated antigen antibody: anti-HBsAg, fusion protein antigen of HCV, fusion protein antigen of HIV1+2, syphilis antigen , HTLV1+2 antigen. These antigens and antibodies are labeled with rhodamine at the determined optimal concentration and ratio for later use, or these antigens and antibodies can be respectively label...
example 3
[0019] Example 3: Application of Rapid Screening Kit for Blood Donors
[0020] This example uses the 96-well plate kit prepared in Example 1, with 3 wells of negative control, 2 wells of positive control, 1 well of blank control, and 8 known test samples (the positive and negative antigen-antibody reactions have been determined by ELISA method, see table one). During the test, except for the blank, add diluent, negative and positive controls and tested samples according to different wells. After the reaction is completed, add enzyme-labeled paired antigen and antibody, chromogenic reagent, and stop solution. Then use microplate reader to measure, and its result is as follows:
[0021] Table 1. Rapid Screening Results of Blood Donors
[0022] Sample HBsAg HCV HIV Syphilis HTLV This kit
[0023] 1 + - - - - 0.249
[0024] 2 - + - - - 0.253
[0025] 3 - - + - - 0.328
[0026] 4 - - - + - 0.225
[0027] 5 - - - - + 0.214
[0028] 6 + + - - - 0.265
[0029] 7 - - + + - 0.3...
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