LHFPL5 Antikörper (C-Term)

Produktnummer ABIN5539148

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)

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.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

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 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: 24 kDa

Gen-ID: 222662

UniProt: Q8TAF8

Pathways: Sensory Perception of Sound