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Mouse SAA PicoKine ELISA Kit standard curve
Mouse SAA PicoKine ELISA Kit standard curve
Mouse SAA PicoKine ELISA Kit standard curve

Mouse SAA/SAA1 ELISA Kit PicoKine(r)

EK1190
Boster Bio
Product group Assays
96 wells
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Mouse SAA PicoKine ELISA Kit
  • Delivery Days Customer
    9
  • Applications
    ELISA
  • Applications Supplier
    ELI
  • Assay Detection Range
    156 pg/ml - 10,000 pg/ml
  • Assay Sensitivity
    <20 pg/ml
  • Assay Time
    15-20
  • Certification
    Research Use Only
  • Scientific Description
    Mouse SAA/SAA1 ELISA Kit PicoKine® (96 Tests). Quantitate Mouse Saa1 in cell culture supernatants, serum, plasma (heparin, EDTA) and urine. Sensitivity: 150pg/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
    mouse SAA
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116158

References

  • You K, Wang Y, Chen X, et al. Neutralizing serum amyloid a protects against sinusoidal endothelial cell damage and platelet aggregation during acetaminophen-induced liver injury. Biochem Biophys Res Commun. 2023,639:20-28. doi: 10.1016/j.bbrc.2022.11.079
    Read this paper
  • Huang J, Qi Z, Chen M, et al. Serum amyloid A1 as a biomarker for radiation dose estimation and lethality prediction in irradiated mouse. Ann Transl Med. 2019,7(23):715. doi: 10.21037/atm.2019.12.27
    Read this paper
  • Burgueño JF, Lang JK, Santander AM, et al. Fluid supplementation accelerates epithelial repair during chemical colitis. PLoS One. 2019,14(4):e0215387. doi: 10.1371/journal.pone.0215387
    Read this paper
  • Gurzeler E, Aavik E, Laine A, et al. Therapeutic effects of rosuvastatin in hypercholesterolemic prediabetic mice in the absence of low density lipoprotein receptor. Biochim Biophys Acta Gen Subj. 2019,1863(2):481-490. doi: 10.1016/j.bbagen.2018.11.012
    Read this paper