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Anti-Sclerostin Antibody (CAB8213)

SKU:
CAB8213
Product Type:
Antibody
Applications:
WB
IHC
Reactivity:
Human
Host Species:
Rabbit
Isotype:
IgG
Research Area:
Metabolism
  • Metabolism Antibodies 3 Anti-Sclerostin Antibody CAB8213
  • Metabolism Antibodies 3 Anti-Sclerostin Antibody CAB8213
€139 - €419
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Description

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Antibody Name:SOST Rabbit Polyclonal Antibody
Antibody SKU:CAB8213
Antibody Size:20uL, 50uL, 100uL
Application:WB IHC
Reactivity:Human, Mouse
Host Species:Rabbit
Immunogen:Recombinant fusion protein containing a sequence corresponding to amino acids 24-213 of human SOST (NP_079513.1).
Application:WB IHC
Recommended Dilution:WB 1:500 - 1:2000 IHC 1:50 - 1:100
Reactivity:Human, Mouse
Positive Samples:HeLa, HepG2, Mouse heart
Immunogen:Recombinant fusion protein containing a sequence corresponding to amino acids 24-213 of human SOST (NP_079513.1).
Purification Method:Affinity purification
Storage Buffer:Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Isotype:IgG
Sequence:QGWQ AFKN DATE IIPE LGEY PEPP PELE NNKT MNRA ENGG RPPH HPFE TKDV SEYS CREL HFTR YVTD GPCR SAKP VTEL VCSG QCGP ARLL PNAI GRGK WWRP SGPD FRCI PDRY RAQR VQLL CPGG EAPR ARKV RLVA SCKC KRLT RFHN QSEL KDFG TEAA RPQK GRKP RPRA RSAK ANQA ELEN AY
Gene ID:50964
Uniprot:Q9BQB4
Cellular Location:Secreted, extracellular matrix, extracellular space
Calculated MW:24kDa
Observed MW:30kDa
Synonyms:SOST, CDD, DAND6, SOST1, VBCH
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.
UniProt Protein Function:SOST: Negative regulator of bone growth that acts through inhibition of Wnt signaling and bone formation. Defects in SOST are the cause of sclerosteosis type 1 (SOST1). An autosomal recessive sclerosing bone dysplasia characterized by a generalized hyperostosis and sclerosis leading to a markedly thickened skull, with mandible, ribs, clavicles and all long bones also being affected. Due to narrowing of the foramina of the cranial nerves, facial nerve palsy, hearing loss and atrophy of the optic nerves can occur. Sclerosteosis is clinically and radiologically very similar to van Buchem disease, mainly differentiated by hand malformations and a large stature in sclerosteosis patients. Defects in SOST are a cause of van Buchem disease (VBCH). An autosomal recessive sclerosing bone dysplasia characterized by endosteal hyperostosis of the mandible, skull, ribs, clavicles, and diaphyses of the long bones. Affected patients present a symmetrically increased thickness of bones, most frequently found as an enlarged jawbone, but also an enlargement of the skull, ribs, diaphysis of long bones, as well as tubular bones of hands and feet. The clinical consequence of increased thickness of the skull include facial nerve palsy causing hearing loss, visual problems, neurological pain, and, very rarely, blindness as a consequence of optic atrophy. Serum alkaline phosphatase levels are elevated. A 52 kb deletion downstream of SOST results in SOST transcription suppression causing van Buchem disease. Defects in SOST are a cause of craniodiaphyseal dysplasia autosomal dominant (CDD). A severe bone dysplasia characterized by massive generalized hyperostosis and sclerosis, especially involving the skull and facial bones. The sclerosis is so severe that the resulting facial distortion is referred to as 'leontiasis ossea' (leonine faces) and the bone deposition results in progressive stenosis of craniofacial foramina. Respiratory obstruction due to choanal stenosis compromises the clinical outcomes of affected patients. Heterozygous mutations located in the secretion signal of the SOST gene prevent sclerostin secretion and can be responsible for craniodiaphyseal dysplasia. Belongs to the sclerostin family. 2 isoforms of the human protein are produced by alternative splicing.
UniProt Protein Details:

Protein type:Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 17q11.2

Cellular Component: extracellular matrix; extracellular region

Molecular Function:protein binding; transcription factor binding

Biological Process: negative regulation of BMP signaling pathway; negative regulation of protein complex assembly; positive regulation of transcription, DNA-dependent; response to mechanical stimulus

Disease: Craniodiaphyseal Dysplasia, Autosomal Dominant; Hyperostosis Corticalis Generalisata; Sclerosteosis 1

NCBI Summary: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. [provided by RefSeq, Jul 2008]
UniProt Code:Q9BQB4
NCBI GenInfo Identifier:20140220
NCBI Gene ID:50964
NCBI Accession:Q9BQB4.1
UniProt Secondary Accession:Q9BQB4,Q495N9,
UniProt Related Accession:Q9BQB4
Molecular Weight:24,264 Da
NCBI Full Name:Sclerostin
NCBI Synonym Full Names:sclerostin
NCBI Official Symbol:SOST  
NCBI Official Synonym Symbols:CDD; VBCH; DAND6; SOST1  
NCBI Protein Information:sclerostin
UniProt Protein Name:Sclerostin
Protein Family:Sclerostin
UniProt Gene Name:SOST  
UniProt Entry Name:SOST_HUMAN
Anti-Sclerostin Polyclonal Antibody (CAB8213)Western blot analysis of extracts of various cell lines, using SOST antibody (CAB8213) at 1:1000 dilution._Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution._Lysates/proteins: 25ug per lane._Blocking buffer: 3% nonfat dry milk in TBST._Detection: ECL Enhanced Kit (RM00021)._Exposure time: 30s.
Anti-Sclerostin Polyclonal Antibody (CAB8213)Immunohistochemistry of paraffin-embedded human prostate using SOST antibody (CAB8213) at dilution of 1:100 (40x lens).

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