PCDH15 anticorps

N° du produit ABIN2463319

Détail du produit anti-PCDH15 anticorps

Antigène: PCDH15 (Protocadherin-15 (PCDH15))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PCDH15 est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PCDH15.

Information d'application

Indications d'application: PCDH15 antibody can be used for detection of PCDH15 by ELISA at 1:62500. PCDH15 antibody can be used for detection of PCDH15 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store PCDH15 antibody at -20 °C.

Détails sur PCDH15

Antigène: PCDH15 (Protocadherin-15 (PCDH15))

Autre désignation: PCDH15 (PCDH15 Produits)

Synonymes: anticorps CDHR15, anticorps DFNB23, anticorps USH1F, anticorps BB078305, anticorps ENSMUSG00000046980, anticorps Gm9815, anticorps Ush1f, anticorps av, anticorps nmf19, anticorps protocadherin-15, anticorps protocadherin related 15, anticorps protocadherin-15, anticorps protocadherin 15, anticorps PCDH15, anticorps CpipJ_CPIJ005081, anticorps Pcdh15

Sujet: PCDH15 is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. PCDH15 consists of a signal peptide, 11 extracellular calcium-binding domains, a transmembrane domain and a unique cytoplasmic domain. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene have been associated with hearing loss, which is consistent with its location at the Usher syndrome type 1F (USH1F) critical region on chromosome 10.

Poids moléculaire: 80 kDa

ID gène: 65217

UniProt: A2A3E5

Pathways: Sensory Perception of Sound