Enzyme-linked immunoassay (ELISA) method of grass carp interleukin 10
An enzyme-linked immunosorbent assay and interleukin technology, which is applied in the direction of interleukin, anti-cytokine/lymphokine/interferon immunoglobulin, cytokine/lymphokine/interferon, etc., can solve the bottleneck of fine identification, No establishment, lack of IL-10 secretion detection and function, etc., to achieve rapid and efficient detection methods and low cost effects
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[0023] Below, the present invention will be described in detail in conjunction with the accompanying drawings and specific embodiments. Unless otherwise specified, the technical means used in the embodiments are conventional means well known to those skilled in the art.
[0024] One: Reagents:
[0025] Maleimide-activated horseradish peroxidase kit was purchased from Thermo Scientific
[0026] Tetramethylbenzidine (TMB) was purchased from Tiangen Biotechnology Company
[0027] Other reagents are analytical reagents
[0028] Two: Steps:
[0029] 1. Preparation of immunogen: Cloning grass carp IL-10 cDNA sequence into prokaryotic expression vector pET-30a(+), constructing recombinant prokaryotic expression vector, and transforming this vector into Escherichia coli BL21(DE3), induced by 1mM IPTG Express recombinant protein IL-10, which is mainly expressed in soluble form, using Ni 2+ The recombinant grass carp IL-10 protein was purified by affinity chromatography and gel fil...
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