Product Description

CDH23 Polyclonal Antibody

Product: Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Catalogue Numbers: BS7438-50, BS7438-100

Sizes: 50µl, 100µl

Swiss-Prot: Q9H251

Host: Rabbit

Reactivity: Human, Mouse, Rat

Applications: WB, IHC

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. Alternative splice variants encoding different isoforms have been described.

Product: Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Purification and Purity: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).

Specificity: CDH23 polyclonal antibody detects endogenous levels of CDH23 protein.

Note: For research use only, not for use in diagnostic procedure.

Extra Notes: Immunohistochemistry (IHC) analysis of CDH23 polyclonal antibody

Storage and Stability: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Alternative Name: Age related hearing loss 1;
Ahl 1;
Ahl;
Ahl1;
Bob;
Bobby;
Bus;
Bustling;
Cadherin 23;
Cadherin23;
CDH 23;
Mdfw;
Modifier of deaf waddler;
nmf112;
nmf181;
nmf252;
Otocadherin;
USH 1D;
USH1 D;
USH1D;
Waltzer;

Immunogen: Recombinant full length Human CDH23.

Conjugate: Unconjugated

Modification: Unmodified