COL6 Antikörper

Produktnummer ABIN7880481

Der Kaninchen Monoklonal anti-COL6 Antikörper wird verwendet zum Nachweis von COL6 in Proben von Human, Maus und Ratte. Er wurde validiert für WB.

Kurzübersicht für COL6 Antikörper (ABIN7880481)

Target: COL6 (Collagen, Type VI (COL6))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser COL6 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: HGG-3

Produktdetails anti-COL6 Antikörper

Verwendungszweck: Collagen VI Antibody / COL6A1

Aufreinigung: Affinity purified

Immunogen: A synthetic peptide specific to human Collagen VI / COL6A1 was used as the immunogen for the Collagen VI antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the Collagen VI antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Antibody in PBS with 0.02 % sodium azide, 50 % glycerol and 0.4-0.5 mg/mL BSA

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store the Collagen VI antibody at -20oC.

Details zu COL6

Target: COL6 (Collagen, Type VI (COL6))

Andere Bezeichnung: Collagen VI

Hintergrund: The collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple-helical domain as their common structural element. Collagen VI is a major structural component of microfibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha1(VI), alpha2(VI), and alpha3(VI) chains. The alpha2(VI) and alpha3(VI) chains are encoded by the COL6A2 and COL6A3 genes, respectively. The protein encoded by this gene is the alpha 1 subunit of type VI collagen (alpha1(VI) chain). Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder, Bethlem myopathy. [RefSeq]

UniProt: P12109