recommended for detection of Sclerostin of mouse and human origin by WB, IP, IF, IHC(P) and ELISA
Modification Notes
Sclerosteosis (SOST), an autosomal recessive sclerosing bone dysplasia, and Van Buchem disease, a closely related disorder, cause abnormal, progressive bone overgrowth. SOST is associated with mutations in the SOST gene and leads to gigantism, entrapment of the seventh and eighth cranial nerves and possibly also distortion of the facies. Van Buchem disease is associated with a 52 kb deletion downstream of the SOST gene that probably affects transcription of the gene. Sclerostin, the protein encoded by the SOST gene, is important for bone homeostasis. It is a secreted protein that inhibits bone formation. Sclerostin is generally expressed at low levels, but high expression of Sclerostin can be detected in bone, cartilage, liver, bone marrow and kidney tissue.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFIHCELISA
See 2 citations for SclerostinAntibody (N-22):
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of Sclerostin of mouse and human origin by WB IP IF IHC(P) and ELISA
Tissue Specificity
recommended for detection of Sclerostin of mouse and human origin by WB, IP, IF, IHC(P) and ELISA