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ICC/IF analysis of HUVEC cells using GTX87430 Dematin antibody. The picture on the right is blocked with the synthesized peptide.
ICC/IF analysis of HUVEC cells using GTX87430 Dematin antibody. The picture on the right is blocked with the synthesized peptide.
ICC/IF analysis of HUVEC cells using GTX87430 Dematin antibody. The picture on the right is blocked with the synthesized peptide.

Dematin antibody

GTX87430
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetDMTN
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Overview

  • Supplier
    GeneTex
  • Product Name
    Dematin antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500~1:1000. ICC/IF: 1:100~1:500. IHC-P: 1:50~1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID2039
  • Target name
    DMTN
  • Target description
    dematin actin binding protein
  • Target synonyms
    dematin; DMT; EPB49; erythrocyte membrane protein band 4.9 (dematin)
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ08495
  • Protein Name
    Dematin
  • Scientific Description
    The protein encoded by this gene is an actin binding and bundling protein that plays a structural role in erythrocytes, by stabilizing and attaching the spectrin/actin cytoskeleton to the erythrocyte membrane in a phosphorylation-dependent manner. This protein contains a core domain in the N-terminus, and a headpiece domain in the C-terminus that binds F-actin. When purified from erythrocytes, this protein exists as a trimer composed of two 48 kDa polypeptides and a 52 kDa polypeptide. The different subunits arise from alternative splicing in the 3 coding region, where the headpiece domain is located. Disruption of this gene has been correlated with the autosomal dominant Marie Unna hereditary hypotrichosis disease, while loss of heterozygosity of this gene is thought to play a role in prostate cancer progression. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2014]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203