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GJC2 antibody (N-Term)

This anti-GJC2 antibody is a Mouse Monoclonal antibody detecting GJC2 in WB. Suitable for Human.
Catalog No. ABIN1538736

Quick Overview for GJC2 antibody (N-Term) (ABIN1538736)

Target

See all GJC2 Antibodies
GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))

Reactivity

  • 19
  • 12
  • 11
  • 2
  • 1
  • 1
Human

Host

  • 17
  • 5
Mouse

Clonality

  • 17
  • 5
Monoclonal

Conjugate

  • 15
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GJC2 antibody is un-conjugated

Application

  • 15
  • 5
  • 4
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

391CT6-4-3
  • Binding Specificity

    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 53-78, N-Term

    Predicted Reactivity

    B, C, Ha, Zf, M, Pig, Rat, X

    Purification

    Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.

    Immunogen

    This GJC2 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 53-78 amino acids from the N-terminal region of human GJC2.

    Isotype

    IgM
  • Application Notes

    WB: 1:100~8000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Mouse monoclonal antibody supplied in crude ascites 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

    GJC2 Antibody (N-term)(Ascites) 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

    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))

    Alternative Name

    GJC2

    Background

    GJC2 is a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.

    Molecular Weight

    47002

    Gene ID

    57165

    NCBI Accession

    NP_065168

    UniProt

    Q5T442
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