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ICC/IF analysis of GH3 cells using GTX54865 TRPM7 antibody. Panel A : Primary antibody Panel B : DNA dye Hoechst 33342 Panel C : Live intact GH3 cells Dilution : 1:100
ICC/IF analysis of GH3 cells using GTX54865 TRPM7 antibody. Panel A : Primary antibody Panel B : DNA dye Hoechst 33342 Panel C : Live intact GH3 cells Dilution : 1:100
ICC/IF analysis of GH3 cells using GTX54865 TRPM7 antibody. Panel A : Primary antibody Panel B : DNA dye Hoechst 33342 Panel C : Live intact GH3 cells Dilution : 1:100

TRPM7 antibody

GTX54865
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetTRPM7
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Overview

  • Supplier
    GeneTex
  • Product Name
    TRPM7 antibody
  • Delivery Days Customer
    7
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.8 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID54822
  • Target name
    TRPM7
  • Target description
    transient receptor potential cation channel subfamily M member 7
  • Target synonyms
    ALSPDC; CHAK; CHAK1; channel-kinase 1; long transient receptor potential channel 7; LTRPC ion channel family member 7; LTRPC7; LTrpC-7; transient receptor potential cation channel subfamily M member 7; transient receptor potential-phospholipase C-interacting kinase; TRP-PLIK
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ96QT4
  • Protein Name
    Transient receptor potential cation channel subfamily M member 7
  • Scientific Description
    This gene belongs to the melastatin subfamily of transient receptor potential family of ion channels. The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. The encoded protein is involved in cytoskeletal organization, cell adhesion, cell migration and organogenesis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. The gene may also be associated with defects of cardiac function. [provided by RefSeq, Aug 2017]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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