DFNB31 Antikörper (AA 378-406)

Produktnummer ABIN5532540

Produktdetails anti-DFNB31 Antikörper

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

Bindungsspezifität: AA 378-406

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DFNB31 Antikörper ist unkonjugiert

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

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This DFNB31 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 378-406 amino acids from the Central region of human DFNB31.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Details zu DFNB31

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

Andere Bezeichnung: DFNB31 (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.

Molekulargewicht: 97 kDa

Gen-ID: 25861

UniProt: Q9P202

Pathways: Sensory Perception of Sound