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CDH23 antibody

This Rabbit Polyclonal antibody specifically detects CDH23 in WB, ELISA and IHC. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7112149

Quick Overview for CDH23 antibody (ABIN7112149)

Target

See all CDH23 Antibodies
CDH23 (Cadherin 23 (CDH23))

Reactivity

  • 45
  • 24
  • 17
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 43
  • 1
  • 1
Rabbit

Clonality

  • 45
Polyclonal

Conjugate

  • 17
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CDH23 antibody is un-conjugated

Application

  • 13
  • 13
  • 12
  • 10
  • 7
  • 7
  • 6
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Purpose

    CDH23 antibody

    Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    cadherin-like 23

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:100 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months

    Expiry Date

    12 months
  • Target

    CDH23 (Cadherin 23 (CDH23))

    Alternative Name

    CDH23

    Background

    Synonyms: Cadherin-23|Otocadherin|CDH23|KIAA1774|KIAA1812

    Background: This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described.

    Molecular Weight

    59 kDa

    Gene ID

    64072

    UniProt

    Q9H251

    Pathways

    Sensory Perception of Sound
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