DFNB31 Antikörper (Middle Region)

Produktnummer ABIN955575

Produktdetails anti-DFNB31 Antikörper

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

Bindungsspezifität: AA 385-413, Middle Region

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)

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 (DFNB31 Produkte)

Synonyme: DFNB31 antikoerper, CIP98 antikoerper, PDZD7B antikoerper, USH2D antikoerper, WHRN antikoerper, WI antikoerper, Cip98 antikoerper, Whrn antikoerper, 1110035G07Rik antikoerper, AW122018 antikoerper, AW742671 antikoerper, C430046P22Rik antikoerper, Dfnb31 antikoerper, wi antikoerper, whirlin antikoerper, WHRN antikoerper, LOC100555508 antikoerper, Whrn antikoerper

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