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Human CXCL5/ENA-78 PicoKine ELISA Kit standard curve
Human CXCL5/ENA-78 PicoKine ELISA Kit standard curve
Human CXCL5/ENA-78 PicoKine ELISA Kit standard curve

Human CXCL5/LIX/ENA-78 ELISA Kit PicoKine(r)

EK0728
Boster Bio
Product group Assays
96 wells
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Human CXCL5/ENA-78 PicoKine ELISA Kit
  • Delivery Days Customer
    9
  • Applications
    ELISA
  • Applications Supplier
    ELI
  • Assay Detection Range
    31.2 pg/ml - 2,000 pg/ml
  • Assay Sensitivity
    <10 pg/ml
  • Assay Time
    20-25
  • Certification
    Research Use Only
  • Scientific Description
    Human CXCL5/LIX/ENA-78 ELISA Kit PicoKine® (96 Tests). Quantitate Human CXCL5 in cell culture supernatants, serum and plasma (heparin, EDTA, citrate). Sensitivity: 10pg/ml. The brand Picokine indicates this is a premium quality ELISA kit. Each Picokine kit delivers precise quantification, high sensitivity, and excellent reproducibility. Only our most reliable and effective kits qualify as Picokine, guaranteeing top-tier results for your assays.
  • Reactivity Supplier
    Human CXCL5
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116158

References

  • Xu Y, Xiang Z, E W, et al. Single-cell transcriptomes reveal a molecular link between diabetic kidney and retinal lesions. Commun Biol. 2023,6(1):912. doi: 10.1038/s42003-023-05300-4
    Read this paper
  • Zhang C, Wang XY, Zhang P, et al. Cancer-derived exosomal HSPC111 promotes colorectal cancer liver metastasis by reprogramming lipid metabolism in cancer-associated fibroblasts. Cell Death Dis. 2022,13(1):57. doi: 10.1038/s41419-022-04506-4
    Read this paper
  • Qi Y, Zhao W, Li M, et al. High C-X-C motif chemokine 5 expression is associated with malignant phenotypes of prostate cancer cells via autocrine and paracrine pathways. Int J Oncol. 2018,53(1):358-370. doi: 10.3892/ijo.2018.4388
    Read this paper
  • Yang Y, Hou J, Shao M, et al. CXCL5 as an autocrine or paracrine cytokine is associated with proliferation and migration of hepatoblastoma HepG2 cells. Oncol Lett. 2017,14(6):7977-7985. doi: 10.3892/ol.2017.7236
    Read this paper