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Immunohistochemistry analysis in human bone marrow and duodenum tissues using Anti-S100A8 antibody. Corresponding S100A8 RNA-seq data are presented for the same tissues.
Immunohistochemistry analysis in human bone marrow and duodenum tissues using Anti-S100A8 antibody. Corresponding S100A8 RNA-seq data are presented for the same tissues.
Immunohistochemistry analysis in human bone marrow and duodenum tissues using Anti-S100A8 antibody. Corresponding S100A8 RNA-seq data are presented for the same tissues.

Anti-S100A8 Antibody

HPA024372
Atlas Antibodies
ApplicationsWestern Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetS100A8
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Overview

  • Supplier
    Atlas Antibodies
  • Product Name
    Anti-S100A8
  • Delivery Days Customer
    4
  • Applications
    Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID6279
  • Target name
    S100A8
  • Target description
    S100 calcium binding protein A8
  • Target synonyms
    60B8AG, CAGA, CFAG, CGLA, CP-10, L1Ag, MA387, MIF, MRP8, NIF, P8, S100-A8, protein S100-A8, calgranulin A, calprotectin L1L subunit, cystic fibrosis antigen, leukocyte L1 complex light chain, migration inhibitory factor-related protein 8, urinary stone protein band A
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP05109
  • Protein Name
    Protein S100-A8
  • Scientific Description
    Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence
  • Reactivity
    Human
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    41116161

Datasheet

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MSDS

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K562 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 0.1% PBST for 20 min at room temperature, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with S100A8 Polyclonal Antibody(bs-2696R)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
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