epitope corresponding to amino acids 21-110 mapping near the N-terminus of Thrombospondin 5 of human origin
Modification Notes
Thrombospondin 5 (also designated THBS5, cartilage oligomeric matrix protein or COMP) is the fifth member of the Thrombospondin family of extracellular matrix proteins. The Thrombospondin family share overall homology, with significant homology in their carboxy-terminal globular domains. They all contain type 2 (epidermal growth factor-like) and type 3 (calmodulin-like) repeats in their central domains. The human COMP/THBS5 gene maps to chromosome 19p13.1. Thrombospondin 5 is expressed in all types of cartilage, tendon and vascular smooth muscle. Its localization in cartilage is developmentally regulated to the chondrocyte territorial and interterritorial matrix. Thrombospondin 5 also binds to Collagen Type I, II and IX in a zinc-dependent manner. Mutations in the COMP/THBS5 gene are associated with the human genetic disorders pseudoachondroplasia (PSACH) and some types of multiple epiphyseal dysplasia (MED). PSACH and MED are autosomal dominant chondrodysplasias, which cause mild to severe short-limb dwarfism and early-onset osteoarthritis.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of Thrombospondin 5 (also designated COMP) of mouse, rat and human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 21-110 mapping near the N-terminus of Thrombospondin 5 of human origin
Tissue Specificity
epitope corresponding to amino acids 21-110 mapping near the N-terminus of Thrombospondin 5 of human origin