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Human cxcl1 gro alpha elisa kit

Manufactured by R&D Systems
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The Human CXCL1/GRO alpha ELISA Kit is an enzyme-linked immunosorbent assay designed for the quantitative detection of human CXCL1/GRO alpha in biological samples such as cell culture supernatants, serum, and plasma.

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Lab products found in correlation

Mouse cxcl1 elisa kit, by R&D Systems (1 mentions) Mouse cxcl1 kc elisa kit, by R&D Systems (1 mentions) Infinite m1000 pro, by Tecan (1 mentions)

Close spelling variants of this product

Human CXCL1/GRO alpha Quantikine ELISA Kit CXCL1 ELISA kit CXCL1 Human kits ELISAs

2 protocols using human cxcl1 gro alpha elisa kit

1

CXCL1 Quantification via ELISA

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The CXCL1 concentrations in the cell supernatants were measured via ELISA according to the manufacturer’s instructions. The following ELISA kits were used in this study: mouse CXCL1 ELISA kit (R&D Systems) and human CXCL1/GRO alpha ELISA kit (R&D Systems).
Liang M., Sun Z., Chen X., Wang L., Wang H., Qin L., Zhao W, & Geng B. (2023). E3 ligase TRIM28 promotes anti-PD-1 resistance in non-small cell lung cancer by enhancing the recruitment of myeloid-derived suppressor cells. Journal of Experimental & Clinical Cancer Research : CR, 42, 275.
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2

Cytokine Profiling in Cell Culture

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Cells were cultured for 24 or 72 h. The cytokine concentrations in the cell supernatants were measured via ELISAs or human cytokine array, according to the manufacturer’s instructions. Infinite® M1000 Pro (Tecan) was used to measure absorbance. The following ELISA kits were used in this study: mouse MCP-1/CCL2 ELISA kit (88-7391-22, Invitrogen), mouse CXCL1/KC ELISA kit (DY453, R&D Systems), human CXCL1/GRO alpha ELISA kit (DY275, R&D Systems), and human CXCL8 ELISA kit (88-8086-88, Invitrogen). The human cytokine array (ARY005) was from R&D Systems (Minneapolis, MN).
Yang Z., Xu G., Wang B., Liu Y., Zhang L., Jing T., Tang M., Xu X., Jiao K., Xiang L., Fu Y., Tang D., Zhang X., Jin W., Zhuang G., Zhao X, & Liu Y. (2021). USP12 downregulation orchestrates a protumourigenic microenvironment and enhances lung tumour resistance to PD-1 blockade. Nature Communications, 12, 4852.
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