CDH23 antibody (Internal Region)

Catalog No. ABIN375183

The Goat Polyclonal anti-CDH23 antibody (ABIN375183) specifically detects CDH23 in WB and EIA. The antibody is reactive with Human samples.

Quick Overview for CDH23 antibody (Internal Region) (ABIN375183)

Target: CDH23 (Cadherin 23 (CDH23))

Reactivity: Human

Host: Goat

Clonality: Polyclonal

Conjugate: This CDH23 antibody is un-conjugated

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Product Details anti-CDH23 Antibody

Binding Specificity: Internal Region

Specificity: This antibody reacts to CDH23 / USH1D.

Purification: Affinity chromatography

Immunogen: Peptide with sequence C-YNISLYENVTVGTS, from the internal region of the protein sequence

Application Details

Application Notes: Peptide ELISA: 1/1000. Western Blot: 1 - 3 μg/mL.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Handling

Concentration: 0,5 mg/mL

Buffer: Tris saline, 0.02 % sodium azide, pH 7.3 with 0.5 % bovine serum albumin

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 freezing and thawing.

Storage: 4 °C/-20 °C

Storage Comment: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Target Details for CDH23

Target: CDH23 (Cadherin 23 (CDH23))

Alternative Name: Cadherin-23

Background: Cadherin like 23 (or Cadherin 23) is, like other members of the cadherin family, a calcium-dependent cell adhesion glycoprotein that preferentially interacts with itself in connecting cells. It is a single pass type I membrane protein that contains 27 cadherin domains. Cadherin like 23 is expressed in the neurosensory epithelium, where it is thought to be involved in stereocilia organisation and hair bundle formation. Defects in the gene encoding Cadherin like 23 are a cause of Usher syndrome, which is characterised by profound congenital sensorineural deafness and eventual blindness. Mutations in this gene are also a cause of non-syndromic sensorineural deafness autosomal recessive type 12 (DFNB12). Cadherin like 23 has also been associated with age-related hearing loss.Synonyms: CDH23, KIAA1774, KIAA1812

Gene ID: 64072

NCBI Accession: NP_001165401

UniProt: Q9H251

Pathways: Sensory Perception of Sound