USH1G Antikörper (AA 1-300) (Biotin)

Produktnummer ABIN7175155

Produktdetails anti-USH1G Antikörper (Biotin)

Target: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Bindungsspezifität: AA 1-300

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser USH1G Antikörper ist konjugiert mit Biotin

Applikation: ELISA

Kreuzreaktivität: Human

Aufreinigung: >95%, Protein G purified

Immunogen: Recombinant Human Usher syndrome type-1G protein (1-300AA)

Isotyp: IgG

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Preservative: 0.03 % Proclin 300
Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

Konservierungsmittel: ProClin

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

Lagerung: -20 °C,-80 °C

Informationen zur Lagerung: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Details zu USH1G

Target: USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))

Andere Bezeichnung: USH1G (USH1G Produkte)

Hintergrund:

Background: Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.

Aliases: ANKS 4A antibody, ANKS4A antibody, FLJ33924 antibody, SANS antibody, Scaffold protein containing ankyrin repeats and SAM domain antibody, USH 1G antibody, USH1G antibody, USH1G_HUMAN antibody, Usher syndrome 1G (autosomal recessive) antibody, Usher syndrome type 1G protein antibody, Usher syndrome type-1G protein antibody

UniProt: Q495M9

Pathways: Sensory Perception of Sound