COL4a6 Antikörper (AA 830-859)

Produktnummer ABIN1538653

Produktdetails anti-COL4a6 Antikörper

Target: COL4a6 (Collagen, Type IV, alpha 6 (COL4a6))

Bindungsspezifität: AA 830-859

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser COL4a6 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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

Immunogen: This COL4A6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 830-859 amino acids from the Central region of human COL4A6.

Klon: RB36723

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: COL4A6 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu COL4a6

Target: COL4a6 (Collagen, Type IV, alpha 6 (COL4a6))

Andere Bezeichnung: COL4A6 (COL4a6 Produkte)

Synonyme: CXDELq22.3 antikoerper, DELXq22.3 antikoerper, BB116301 antikoerper, collagen type IV alpha 6 chain antikoerper, collagen, type IV, alpha 6 antikoerper, COL4A6 antikoerper, Col4a6 antikoerper, col4a6 antikoerper

Hintergrund: This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Two splice variants have been identified for this gene.

Molekulargewicht: 163807

Gen-ID: 1288

NCBI Accession: NP_001838, NP_378667

UniProt: Q14031