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CSRP3 antibody

Research Use Only
GTX110536
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetCSRP3
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Overview

  • Supplier
    GeneTex
  • Product Name
    CSRP3 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *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
  • Concentration
    0.55 mg/ml
  • Conjugate
    Unconjugated
  • Formulation
    Liquid
  • Gene ID8048
  • Target name
    CSRP3
  • Target description
    cysteine and glycine rich protein 3
  • Target synonyms
    cardiac LIM domain protein; CLP; CMD1M; CMH12; CRP3; cysteine and glycine-rich protein 3; cysteine and glycine-rich protein 3 (cardiac LIM protein); LIM domain only 4; LMO4; MLP
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP50461
  • Protein Name
    Cysteine and glycine-rich protein 3
  • Scientific Description
    This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5 UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability. Olie CS et al., 2020 Oct 19, Sci Rep
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