COL17A1 Antikörper

Produktnummer ABIN7244681

Produktdetails anti-COL17A1 Antikörper

Target: COL17A1 (Collagen, Type XVII, alpha 1 (COL17A1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser COL17A1 Antikörper ist unkonjugiert

Applikation: ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Synthetic peptide of human COL17A1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.6 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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 at -20°C. Avoid freeze / thaw cycles.

Details zu COL17A1

Target: COL17A1 (Collagen, Type XVII, alpha 1 (COL17A1))

Andere Bezeichnung: COL17A1 (COL17A1 Produkte)

Synonyme: col17a1 antikoerper, fk89a06 antikoerper, si:ch211-223p8.6 antikoerper, wu:fk89a06 antikoerper, COL17A1 antikoerper, BA16H23.2 antikoerper, BP180 antikoerper, BPA-2 antikoerper, BPAG2 antikoerper, LAD-1 antikoerper, Bpag antikoerper, Bpag2 antikoerper, collagen type XVII alpha 1 chain antikoerper, collagen, type XVII, alpha 1b antikoerper, collagen, type XVII, alpha 1 antikoerper, Col17a1 antikoerper, col17a1b antikoerper, COL17A1 antikoerper

Hintergrund: COL17A1 (Collagen Type XVII Alpha 1 Chain) is a Protein Coding gene. Diseases associated with COL17A1 include Epidermolysis Bullosa, Junctional, Non-Herlitz Type and Epithelial Recurrent Erosion Dystrophy. Among its related pathways are Collagen chain trimerization and Phospholipase-C Pathway. An important paralog of this gene is COL6A1.This gene encodes the alpha chain of type XVII collagen. Unlike most collagens, collagen XVII is a transmembrane protein. Collagen XVII is a structural component of hemidesmosomes, multiprotein complexes at the dermal-epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane. Mutations in this gene are associated with both generalized atrophic benign and junctional epidermolysis bullosa. Two homotrimeric forms of type XVII collagen exist. The full length form is the transmembrane protein. A soluble form, referred to as either ectodomain or LAD-1, is generated by proteolytic processing of the full length form.

UniProt: Q9UMD9