LHFPL5 Antikörper (C-Term)

Produktnummer ABIN654373

Produktdetails anti-LHFPL5 Antikörper

Target: LHFPL5 (Lipoma HMGIC Fusion Partner-Like 5 (LHFPL5))

Bindungsspezifität: AA 186-214, C-Term

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser LHFPL5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Homologie: Rat

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

Immunogen: This LHFPL5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 186-214 amino acids from the C-terminal region of human LHFPL5.

Klon: RB28242

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody 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: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Haltbarkeit: 6 months

Details zu LHFPL5

Target: LHFPL5 (Lipoma HMGIC Fusion Partner-Like 5 (LHFPL5))

Andere Bezeichnung: LHFPL5 (LHFPL5 Produkte)

Synonyme: DFNB67 antikoerper, TMHS antikoerper, dJ510O8.8 antikoerper, 9330179O15Rik antikoerper, Tmhs antikoerper, hscy antikoerper, PMP22A antikoerper, lhfpl5 antikoerper, zgc:171589 antikoerper, LHFPL tetraspan subfamily member 5 antikoerper, lipoma HMGIC fusion partner-like 5 antikoerper, LHFPL tetraspan subfamily member 5b antikoerper, LHFPL5 antikoerper, Lhfpl5 antikoerper, lhfpl5b antikoerper

Hintergrund: This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis.

Molekulargewicht: 24201

Gen-ID: 222662

NCBI Accession: NP_872354

UniProt: Q8TAF8

Pathways: Sensory Perception of Sound