Size :50ul
Clone Number:
Aliases:cartilage oligomeric matrix protein (pseudoachondroplasia; epiphyseal dysplasia 1; multiple) antibody; Cartilage oligomeric matrix protein antibody; Cartilage oligomeric matrix protein precursor antibody; COMP antibody; COMP_HUMAN antibody; EDM 1 antibody; EDM1 antibody; EPD 1 antibody; EPD1 antibody; Epiphyseal dysplasia 1 antibody; Epiphyseal dysplasia 1 multiple antibody; Epiphyseal dysplasia multiple 1 antibody; MED antibody; MGC13181 antibody; MGC149768 antibody; PSACH antibody; pseudoachondroplasia (epiphyseal dysplasia 1; multiple) antibody; Pseudoachondroplasia antibody; THBS 5 antibody; THBS5 antibody; Thrombospondin 5 antibody; Thrombospondin-5 antibody; Thrombospondin5 antibody; TSP5 antibody
Product Type:Polyclonal Antibody
Immunogen Species:Homo sapiens (Human)
UniProt ID:P49747
Immunogen:Fusion protein of Human COMP
Raised in:Rabbit
Species Reactivity:Human, Mouse, Rat
Tested Applications:ELISA, IHC; ELISA:1:2000-1:10000, IHC:1:100-1:300
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).
Clonality:Polyclonal
Isotype:IgG
Purification Method:Antigen affinity purification
Conjugate:Non-conjugated
Buffer:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Form:Liquid
Stroage:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Target Names:COMP
Research Areas:Cell biology;Signal transduction?Stem cells