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FACS analysis of human peripheral blood monocytes using GTX43517 CD68 antibody [Ki-M7] (FITC).
FACS analysis of human peripheral blood monocytes using GTX43517 CD68 antibody [Ki-M7] (FITC).
FACS analysis of human peripheral blood monocytes using GTX43517 CD68 antibody [Ki-M7] (FITC).

CD68 antibody [Ki-M7] (FITC)

GTX43517
GeneTex
ApplicationsFlow Cytometry
Product group Antibodies
TargetCD68
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Overview

  • Supplier
    GeneTex
  • Product Name
    CD68 antibody [Ki-M7] (FITC)
  • Delivery Days Customer
    9
  • Applications
    Flow Cytometry
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    Ki-M7
  • Conjugate
    FITC
  • Gene ID968
  • Target name
    CD68
  • Target description
    CD68 molecule
  • Target synonyms
    CD68 antigen; GP110; LAMP4; macrophage antigen CD68; macrosialin; SCARD1; scavenger receptor class D, member 1
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP34810
  • Protein Name
    Macrosialin
  • Scientific Description
    This gene encodes a 110-kD transmembrane glycoprotein that is highly expressed by human monocytes and tissue macrophages. It is a member of the lysosomal/endosomal-associated membrane glycoprotein (LAMP) family. The protein primarily localizes to lysosomes and endosomes with a smaller fraction circulating to the cell surface. It is a type I integral membrane protein with a heavily glycosylated extracellular domain and binds to tissue- and organ-specific lectins or selectins. The protein is also a member of the scavenger receptor family. Scavenger receptors typically function to clear cellular debris, promote phagocytosis, and mediate the recruitment and activation of macrophages. Alternative splicing results in multiple transcripts encoding different isoforms. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. IHC analysis of CD68 using anti-CD68 antibody (A00602-1). CD68 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 microg/ml rabbit anti-CD68 Antibody (A00602-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.
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