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GJB2 antibody (AA 80-130)

The Rabbit Polyclonal anti-GJB2 antibody has been validated for WB and ELISA. It is suitable to detect GJB2 in samples from Human.
Catalog No. ABIN6992084

Quick Overview for GJB2 antibody (AA 80-130) (ABIN6992084)

Target

See all GJB2 Antibodies
GJB2 (Gap Junction Protein, beta 2, 26kDa (GJB2))

Reactivity

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  • 23
  • 5
  • 2
  • 2
  • 2
  • 1
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
This GJB2 antibody is un-conjugated

Application

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  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

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    AA 80-130

    Specificity

    GJB2 antibody is human specific.

    Purification

    GJB2 antibody is affinity chromatography purified via peptide column.

    Immunogen

    GJB2 antibody was raised against a 16 amino acid peptide near the center of human GJB2. The immunogen is located within amino acids 80 - 130 of GJB2.

    Isotype

    IgG
  • Application Notes

    GJB2 antibody can be used for detection of GJB2 by Western blot at 1 - 2 μ,g/mL.

    Antibody validated: Western Blot in human samples. All other applications and species not yet tested.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    GJB2 antibody is supplied in PBS containing 0.02 % 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

    -20 °C,4 °C

    Storage Comment

    GJB2 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.
  • Target

    GJB2 (Gap Junction Protein, beta 2, 26kDa (GJB2))

    Alternative Name

    GJB2

    Background

    The Gap junction beta-2 protein (GJB2), also known as Connexin 26, is member of the gap junction protein family which form structures that were shown to consist of cell-to-cell channels that facilitate the transfer of ions and small molecules between cells (1). Mutations in the GJB2 gene are thought to be responsible for as much as 35-45 % of congenital sensorineural hearing loss in some populations (2). Other mutations in this gene have also been linked to a wide array of skin diseases (3).

    Molecular Weight

    Predicted: 25 kDa

    Observed: 26 kDa

    Gene ID

    2706

    NCBI Accession

    NP_003995

    UniProt

    P29033

    Pathways

    Sensory Perception of Sound, Cell-Cell Junction Organization
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