QuickDetect™ IL-6 (Human) ELISA Kit

QuickDetect™ IL-6 (Human) ELISA Kitis available at Gentaur for Next week Delivery.

A rapid sandwich ELISA kit for the quantitative measurement of IL-6 in human serum, plasma, cell culture supernatnat and other biological fluids.

Description:

Interleukin-6 (IL-6) is a cytokine with a wide variety of biological functions. It is a potent inducer of the acute phase response. Plays an essential role in the final differentiation of B-cells into Ig-secreting cells Involved in lymphocyte and monocyte differentiation. Acts on B-cells, T-cells, hepatocytes, hematopoietic progenitor cells and cells of the CNS. Required for the generation of T(H)17 cells. Also acts as a myokine. It is discharged into the bloodstream after muscle contraction and acts to increase the breakdown of fats and to improve insulin resistance. It induces myeloma and plasmacytoma growth and induces nerve cells differentiation. BioVision’s QuickDetect™ IL-6 ELISA kit is a sandwich ELISA assay for measuring the quantity of human IL-6 in serum, plasma and cell culture and other biological fluid. The entire process can be performed within 90 minutes with fewer incubation and wash steps respectively, resulting less errors and more consistent results.

Applications: This ELISA kit is used for quantitative measurement of IL-6 in human serum, plasma, cell culture supernatant and other biological fluids.

Sample Typ:e Human serum, plasma, cell culture supernatant, tissue homogenate and other biological fluids.

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Features and Benefits:

Easy, convenient and time-saving method to measure the level of IL-6 in human serum, plasma, culture supernatants and other biological fluids. The entire assay can be performed within 90 minutes with with fewer incubation and wash step respectively, resulting in less errors and more consistent results. Detection Range: 1 – 70 pg/ml Sensitivity: < 0.1 pg/ml Assay Precision: Intra-Assay: CV < 10%; Inter-Assay: CV < 12% (CV (%) = SD/mean X 100) Cross Reactivity: No significant cross-reactivity or interference between this analyte and its analogues was observed.