COL1A2 Antikörper (AA 23-79)

Produktnummer ABIN7193541

Produktdetails anti-COL1A2 Antikörper

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

Bindungsspezifität: AA 23-79

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser COL1A2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)

Aufreinigung: purified

Immunogen: Purified recombinant fragment of human COL1A2 (AA: 23-79) expressed in E. coli.

Klon: 4D1A7

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise: WB:1:500 - 1:2000, ICC:1:200 - 1:1000, FCM:1:200 - 1:400, ELISA:1:10000,

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: Purified antibody in PBS with 0.05 % 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: 4°C, -20°C for long term storage

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:

Description: 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.

Aliases: OI4, EDSCV, EDSARTH2

Molekulargewicht: 129 kDa

Gen-ID: 1278