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CSRP3 antibody (AA 91-119)

The Rabbit Polyclonal anti-CSRP3 antibody has been validated for WB. It is suitable to detect CSRP3 in samples from Human.
Catalog No. ABIN1538690

Quick Overview for CSRP3 antibody (AA 91-119) (ABIN1538690)

Target

See all CSRP3 Antibodies
CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))

Reactivity

  • 32
  • 20
  • 9
  • 5
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Human

Host

  • 29
  • 2
  • 1
Rabbit

Clonality

  • 30
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Polyclonal

Conjugate

  • 20
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CSRP3 antibody is un-conjugated

Application

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Western Blotting (WB)

Clone

RB36750
  • Binding Specificity

    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 91-119

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This CSRP3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 91-119 amino acids from the Central region of human CSRP3.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    CSRP3 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))

    Alternative Name

    CSRP3

    Background

    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.

    Molecular Weight

    20969

    Gene ID

    8048

    NCBI Accession

    NP_003467

    UniProt

    P50461
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