CDH23 anticorps (AA 61-110)

N° du produit ABIN1534291

L’anticorps anti-CDH23 Polyclonal Lapin est utilisé pour la détection de CDH23 dans des échantillons de Humain, Souris et Rat. Il a été validé pour ELISA et IF.

Aperçu rapide pour CDH23 anticorps (AA 61-110) (ABIN1534291)

Antigène: CDH23 (Cadherin 23 (CDH23))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CDH23 est non-conjugé

Application: ELISA, Immunofluorescence (IF)

Détail du produit anti-CDH23 anticorps

Épitope: AA 61-110

Fonction: Cadherin-23 Antibody

Specificité: Cadherin-23 Polyclonal Antibody detects endogenous levels of Cadherin-23 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Pureté: > 95 %

Immunogène: The antiserum was produced against synthesized peptide derived from human CDH23. AA range:61-110

Isotype: IgG

Information d'application

Indications d'application: IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur CDH23

Antigène: CDH23 (Cadherin 23 (CDH23))

Autre désignation: CDH23

Sujet:

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

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. [provided by RefSeq, May 2013],

Gene Name: CDH23

Protein Name: Cadherin-23

Poids moléculaire: 369 kDa

ID gène: 64072

OMIM: 276900

UniProt: Q9H251

Pathways: Sensory Perception of Sound