1. Principle
This test kit is based on the competitive enzyme immunoassay for the detection of Gentamicin in the sample. The coupling antigen is pre-coated on the micro-well stripes. The Gentamicin in the sample and pre-coated coupling antigen on the micro-well stripes compete for the anti-Gentamicin antibody. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the sample has a negative correlation with the Gentamicin in it. The value is compared to the standard curve and the Gentamicin concentration is subsequently obtained.
1. Principle
This test kit is based on the competitive enzyme immunoassay for the detection of Florfenicol in samples. The coupling antigens are pre-coated on the micro-well stripes. The Florfenicol in the sample and the conjugate antigens pre-coated on the micro-well stripes compete for the anti-Florfenicol antibodies. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value has a negative correlation with the Florfenicol concentration in the sample. This value is compared to the standard curve and the Florfenicol concentration is subsequently obtained.
1. Principle
This test kit is based on the competitive enzyme immunoassay for the detection of Tylosin in the sample. The coupling antigens are pre-coated on the micro-well stripes. The Tylosin in the sample and the coupling antigens pre-coated on the micro-well stripes compete for the anti-Tylosin antibody. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the sample has a negative correlation with the Tylosin in it. This value is compared to the standard curve and the Tylosin concentration is subsequently obtained.
The kit uses a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) to assay the level of Human
Androgen in samples. Add Androgen to monoclonal antibody Enzyme well which is pre-coated with Human
Androgenmonoclonal antibody, incubation; then, add Androgenantibodies labeled with biotin, and combined with
Streptavidin-HRP to form immune complex; then carry out incubation and washing again to remove the uncombined enzyme.
Then add Chromogen Solution A, B, the color of the liquid changes into the blue, And at the effect of acid, the color finally
becomes yellow. The chroma of color and the concentration of the Human Substance Androgen of sample were positively
correlated.
Standard; 128nmol/L.
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1. Principle
This test kit is based on the competitive enzyme immunoassay for the detection of chloramphenicol in the tissue (chicken, pork), honey, milk, fish, shrimp and egg. The coupling antigen is pre-coated on the micro-well stripes. The chloramphenicol in the testing sample competes with the coupling antigen pre-coated on the micro-well stripes for the antibody against chloramphenicol. After the addition of the enzyme conjugate, the tmb substrate is added for coloration. The optical density (od) value of the testing sample has a negative correlation with the content of chloramphenicol in it. This value is compared to the standard curve and the content of the corresponding chloramphenicol is subsequently obtained.
Size 96 wells/Plate
Format Indirect
Incubation Time 30 + 30 + 5 + 10 + 1
Sample Type Serum
Storage 2-8 C
Cat No STGS-R
The Scrub Typhus Detectâ?¢ IgG ELISA test for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA assay system for the detection of IgG antibodies in human serum to OT-derived recombinant antigen. For research use only. Not for use in diagnostic procedures.
The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
