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| Cat.No | ACP12509 | Target Name | SOST |
|---|---|---|---|
| Target Synonyms | BEER; CDD; Cortical hyperostosis with syndactyly; Sclerosteosis; Sclerostin; Sost; SOST_HUMAN; SOST1; UNQ2976/PRO7455/PRO7476; VBCH | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Expression Range | 24-213 |
| Protein Length | Full Length of Mature Protein | Purity | >85% (SDS-PAGE) |
| Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q9BQB4 |
|---|
Uniprot Id
Q9BQB4
Target Species
Human
Target Name
SOST
Target Full Name
Sclerostin
Target Function
Negative regulator of bone growth that acts through inhibition of Wnt signaling and bone formation.
Target Involvement
Sclerosteosis 1 (SOST1); Van Buchem disease (VBCH); Craniodiaphyseal dysplasia autosomal dominant (CDD)
Target Subcellular Location
Secreted, extracellular space, extracellular matrix.
Target Protein Families
Sclerostin family
Target Tissue Specificity
Widely expressed at low levels with highest levels in bone, cartilage, kidney, liver, bone marrow and primary osteoblasts differentiated for 21 days. Detected in the subendothelial layer of the aortic intima (at protein level).
Target Research Area
Signal Transduction
Target Synonyms
BEER; CDD; Cortical hyperostosis with syndactyly; Sclerosteosis; Sclerostin; Sost; SOST_HUMAN; SOST1; UNQ2976/PRO7455/PRO7476; VBCH
Target Background
Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease.
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