ELISA detection method for detecting human serum candida glabrata enolase IgG antibody
The technology of a fungal enolase and a detection method, applied in the biological field, can solve the problems of insufficient research investment in the detection of non-albicans Candida infection, and achieve the effects of good batch-to-batch stability and high sensitivity
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[0033] The present invention will be further described below in conjunction with embodiment.
[0034] An ELISA detection method for detecting human serum Candida glabrata enolase IgG antibody, using indirect ELISA detection method to detect human serum Candida glabrata enolase Cg-Eno IgG antibody, during the detection process, using a special ELISA kit to detect Cg -Eno IgG antibody.
[0035] The ELISA kit includes enzyme-labeled plate, enzyme-labeled antibody, washing solution, substrate chromogenic solution, sample diluent, stop solution, positive control solution and negative control solution, and the enzyme-labeled plate utilizes purified Cg-Eno to recombine The protein antigen is coated to make a coated enzyme-linked plate. The specifications of each reagent are as follows:
[0036] The coating process of the microtiter plate is as follows: the purified Cg-Eno recombinant protein antigen is diluted to 1 μg / mL with pH 9.5, 0.05 mol / L carbonate buffer, and added to the 96...
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