DFNB31 Antikörper (Middle Region)

Produktnummer ABIN955575

Dieses Anti-DFNB31-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von DFNB31 in WB, IHC (p) und EIA. Geeignet für Human.

Kurzübersicht für DFNB31 Antikörper (Middle Region) (ABIN955575)

Target: DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DFNB31 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Produktdetails anti-DFNB31 Antikörper

Bindungsspezifität: AA 385-413, Middle Region

Spezifität: This antibody recognizes Human Whirlin (Center).

Aufreinigung: Affinity Chromatography on Protein A

Immunogen: KLH conjugated synthetic peptide between 385-413 amino acids from the Central region of Human Whirlin. Genename: WHRN

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS, 0.09 % Sodium Azide

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu DFNB31

Target: DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))

Andere Bezeichnung: Whirlin

Hintergrund: This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.Synonyms: Autosomal recessive deafness type 31 protein, DFNB31, KIAA1526, WHRN

Molekulargewicht: 96586 Da

Gen-ID: 25861

NCBI Accession: NP_001077354

Pathways: Sensory Perception of Sound