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FACS analysis of HeLa cells using GTX57543 Calmodulin antibody. Cell Number: 1 x 10? cells Red: Primary antibody Antibody amount: 2-5 microg
FACS analysis of HeLa cells using GTX57543 Calmodulin antibody. Cell Number: 1 x 10? cells Red: Primary antibody Antibody amount: 2-5 microg
FACS analysis of HeLa cells using GTX57543 Calmodulin antibody. Cell Number: 1 x 10? cells Red: Primary antibody Antibody amount: 2-5 microg

Calmodulin antibody [J4D8]

GTX57543
GeneTex
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman, Mouse
TargetCALM1
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Overview

  • Supplier
    GeneTex
  • Product Name
    Calmodulin antibody [J4D8]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    J4D8
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID801
  • Target name
    CALM1
  • Target description
    calmodulin 1
  • Target synonyms
    CALML2; calmodulin 1 (phosphorylase kinase, delta); calmodulin-1; Calmodulin-2; Calmodulin-3; caM; CAM2; CAM3; CAMB; CAMC; CAMI; CAMIII; CPVT4; DD132; LQT14; PHKD; phosphorylase kinase subunit delta; phosphorylase kinase, delta subunit; prepro-calmodulin 1
  • Host
    Mouse
  • Isotype
    IgG2a
  • Protein IDP0DP23
  • Protein Name
    Calmodulin-1
  • Scientific Description
    This gene is a member of the calmodulin gene family. There are three distinct calmodulin genes dispersed throughout the genome that encode the identical protein, but differ at the nucleotide level. Calmodulin is a calcium binding protein that plays a role in signaling pathways, cell cycle progression and proliferation. Several infants with severe forms of long-QT syndrome (LQTS) who displayed life-threatening ventricular arrhythmias together with delayed neurodevelopment and epilepsy were found to have mutations in either this gene or another member of the calmodulin gene family (PMID:23388215). Mutations in this gene have also been identified in patients with less severe forms of LQTS (PMID:24917665), while mutations in another calmodulin gene family member have been associated with catecholaminergic polymorphic ventricular tachycardia (CPVT)(PMID:23040497), a rare disorder thought to be the cause of a significant fraction of sudden cardiac deaths in young individuals. Pseudogenes of this gene are found on chromosomes 10, 13, and 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203