COL1A2 Antikörper

Produktnummer ABIN7234801

Produktdetails anti-COL1A2 Antikörper

Target: COL1A2 (Collagen, Type I, alpha 2 (COL1A2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser COL1A2 Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC), ELISA

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human COL1A2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:100-1:300

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.1 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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 COL1A2

Target: COL1A2 (Collagen, Type I, alpha 2 (COL1A2))

Andere Bezeichnung: COL1A2 (COL1A2 Produkte)

Synonyme: AA960264 antikoerper, AI325291 antikoerper, Col1a-2 antikoerper, Cola-2 antikoerper, Cola2 antikoerper, oim antikoerper, OI4 antikoerper, Gas-6 antikoerper, alpha2(I) antikoerper, hm:zehn2357 antikoerper, wu:fa98d05 antikoerper, wu:fa99g10 antikoerper, wu:fb04c08 antikoerper, wu:fb11d06 antikoerper, zehn2357 antikoerper, coagulation factor II, thrombin antikoerper, collagen, type I, alpha 2 antikoerper, collagen type I alpha 2 chain antikoerper, collagen type I alpha 2 L homeolog antikoerper, growth arrest specific 6 antikoerper, F2 antikoerper, Col1a2 antikoerper, col1a2.L antikoerper, COL1A2 antikoerper, Gas6 antikoerper, col1a2 antikoerper

Hintergrund: This gene encodes the pro-alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.

UniProt: P08123