Product Description
COMP Polyclonal Antibody | E-AB-11095 | Elabscience
Type: Polyclonal Antibody
Synonyms: cartilage oligomeric matrix protein (pseudoachondroplasia, epiphyseal dysplasia 1, multiple), Cartilage oligomeric matrix protein, Cartilage oligomeric matrix protein precursor, COMP, COMP, EDM 1, EDM1, EPD 1, EPD1, Epiphyseal dysplasia 1, Epiphyseal dysplasia 1 multiple, Epiphyseal dysplasia multiple 1, MED, MGC13181, MGC149768, PSACH, pseudoachondroplasia (epiphyseal dysplasia 1, multiple), Pseudoachondroplasia, THBS 5, THBS5, Thrombospondin 5, Thrombospondin-5, Thrombospondin5, TSP5
Application: WB, IHC, ELISA
Reactivity: Human, Mouse, Rat
Host: Rabbit
Isotype: IgG
Reserch Areas: Cancer, Cell Biology, Signal Transduction, Stem Cells
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).
Concentration: 0.3 mg/mL
Storage: Store at -20°C. Avoid freeze / thaw cycles.
Immunogen: Recombinant protein of human COMP
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method: Affinity purification
Dilution: WB 1:500-1:2000, IHC 1:50-1:200
Clone: N/A
Conjugation: Unconjugated
Molecular Weight(Calculated): 83 kDa
Molecular Weight(Observed): N/A