COMP Antikörper

Produktnummer ABIN702535

Produktdetails anti-COMP Antikörper

Target: COMP (Cartilage Oligomeric Matrix Protein (COMP))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser COMP Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human COMP

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB(1:100-1000), IHC-P(1:100-500), IF(IHC-P)(1:50-200)

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % 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: -20 °C

Informationen zur Lagerung: Store at -20°C for 12 months.

Haltbarkeit: 12 months

Details zu COMP

Target: COMP (Cartilage Oligomeric Matrix Protein (COMP))

Andere Bezeichnung: Comp/Epd1/Thbs5 (COMP Produkte)

Synonyme: COMP antikoerper, EDM1 antikoerper, EPD1 antikoerper, MED antikoerper, PSACH antikoerper, THBS5 antikoerper, TSP5 antikoerper, cartilage oligomeric matrix protein antikoerper, COMP antikoerper, sce3551 antikoerper, CJA_1292 antikoerper, Comp antikoerper

Hintergrund:

Synonyms: Cartilage oligomeric matrix protein, Cartilage oligomeric matrix protein precursor, EDM 1, EDM1, EPD 1, EPD1, Epiphyseal dysplasia 1, Epiphyseal dysplasia 1 multiple, Epiphyseal dysplasia multiple 1, MED, MGC13181, MGC149768, PSACH, Pseudoachondroplasia, THBS 5, THBS5, Thrombospondin 5, Thrombospondin5.

Background: The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Mutations can cause the osteochondrodysplasias pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). [provided by RefSeq, Jul 2008].

Gen-ID: 1311