CDH23 Antikörper (AA 61-110)

Produktnummer ABIN1534291

Der Kaninchen Polyklonal anti-CDH23 Antikörper wird verwendet zum Nachweis von CDH23 in Proben von Human, Maus und Ratte. Er wurde validiert für ELISA und IF.

Kurzübersicht für CDH23 Antikörper (AA 61-110) (ABIN1534291)

Target: CDH23 (Cadherin 23 (CDH23))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CDH23 Antikörper ist unkonjugiert

Applikation: ELISA, Immunofluorescence (IF)

Produktdetails anti-CDH23 Antikörper

Bindungsspezifität: AA 61-110

Verwendungszweck: Cadherin-23 Antibody

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

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

Reinheit: > 95 %

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C/1 year

Haltbarkeit: 12 months

Details zu CDH23

Target: CDH23 (Cadherin 23 (CDH23))

Andere Bezeichnung: CDH23

Hintergrund:

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

Molekulargewicht: 369 kDa

Gen-ID: 64072

OMIM: 276900

UniProt: Q9H251

Pathways: Sensory Perception of Sound