SOST抗体

SOST抗体

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  • 询价
  • Abcam
  • 中国/美国/德国
  • xy10593-RP02
  • 2025年07月11日
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    • 保存条件

      常温,避光

    • 克隆性

      单克隆

    • 抗体名

      SOST抗体

    SOST抗体产品信息免疫原 : Human cell-derived rhSOST ( Catalog#10593-H07H )

    抗体宿主 : Rabbit IgG
    缓冲液 : 0.2 μm filtered solution in PBS, 5% trehalose may be added in some batches. Please read the hardcopy of COA or contact our customer service to confirm the formulation.
    制备方法 : Produced in rabbits immunized with purified, human cell-derived, recombinant human SOST (rhSOST; Catalog#10593-H07H; NP_079513.1; Gln 24- Tyr 213). Total IgG was purified by Protein A affinity chromatography.
    SOST抗体 Background

    SOST, also known as sclerostin, is a glycoprotein with a signal peptide for secretion and a C-terminal cysteine knot-like (CTCK) domain and belongs to the Cerberus/DAN family of bone morphogenetic protein (BMP) antagonists including Dan, Cerberus, Gremlin, PRDC, and Caronte. SOST is expressed at significant levels in bone, cartilage, kidney, and liver, and was originally identified as an important regulator of bone remodeling, homeostasis, and links bone resorption and bone apposition. It negatively regulates the formation of bone by repressing the differentiation and/or function of osteoblasts induced by BMPs. It has been shown that SOST binds BMP-5, -6, and -7 with high affinity and BMP-2 and -4 with low affinity. Recent studies have revealed that SOST inhibits the bone growth probably by binding to the extracellular domain of the Wnt coreceptors LRP5 and LRP6 and disrupts the Wnt signaling. Loss-of-function mutations of SOST are associated with sclerosteosis which is an autosomal-recessive bone dysplasia characterized by progressive skeletal overgrowth, and reduced sclerostin expression results in a milder form of the disorder called van Buchem disease.
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