DFNA5 Antikörper (AA 200-280)

Produktnummer ABIN7217644

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch DFNA5 in WB und ELISA. Es zeigt Reaktivität gegenüber Proben von Human und Ratte.

Kurzübersicht für DFNA5 Antikörper (AA 200-280) (ABIN7217644)

Target: DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))

Reaktivität: Human, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DFNA5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-DFNA5 Antikörper

Bindungsspezifität: AA 200-280

Verwendungszweck: Rabbit Anti-DFNA5 Polyclonal Antibody

Spezifität: DFNA5 Polyclonal Antibody detects endogenous levels of DFNA5 protein.

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

Immunogen: Synthesized peptide derived from the Internal region of human DFNA5 at AA range: 200-280

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,ELISA 1:40000,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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Haltbarkeit: 12 months

Details zu DFNA5

Target: DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))

Andere Bezeichnung: DFNA5

Hintergrund: DFNA5, ICERE1, Non-syndromic hearing impairment protein 5, Inversely correlated with estrogen receptor expression 1, ICERE-1Hearing impairment is a heterogeneous condition with over 40 loci described. Non-syndromic hearing impairment protein 5 encoded by DFNA5 is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.

Molekulargewicht: 54kD

Gen-ID: 1687

UniProt: O60443

Pathways: Sensory Perception of Sound