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COCH antibody

This Rabbit Polyclonal antibody specifically detects COCH in IHC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7262425

Quick Overview for COCH antibody (ABIN7262425)

Target

See all COCH Antibodies
COCH (Cochlin (COCH))

Reactivity

  • 39
  • 13
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 37
  • 2
Rabbit

Clonality

  • 39
Polyclonal

Conjugate

  • 21
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This COCH antibody is un-conjugated

Application

  • 29
  • 18
  • 11
  • 10
  • 2
  • 2
  • 2
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human COCH (NP_001128530.1).

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:100 IF 1:50-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    COCH (Cochlin (COCH))

    Alternative Name

    COCH

    Background

    The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94 % and 79 % amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated.

    Gene ID

    1690

    UniProt

    O43405

    Pathways

    Sensory Perception of Sound
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