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目錄:亞科因(武漢)生物技術(shù)有限公司>>細胞因子及蛋白>>細胞因子>> PRP1955-50 μg重組人胰島素樣生長因子1

重組人胰島素樣生長因子1

  • 重組人胰島素樣生長因子1
參考價 358
具體成交價以合同協(xié)議為準(zhǔn)
參考價 358
具體成交價以合同協(xié)議為準(zhǔn)
  • 品牌 Abbkine/亞科因
  • 型號 PRP1955-50 μg
  • 廠商性質(zhì) 生產(chǎn)商
  • 所在地 武漢市
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更新時間:2025-12-23 09:14:15瀏覽次數(shù):74評價

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Abbkine/亞科因重組人胰島素樣生長因子1通過LAL法測定,每微克蛋白里內(nèi)毒素含量<1.0 EU。
IGF I, also known as Mechano Growth Factor, somatomedin-C, IGF-I, and IGF1, is a secreted protein that belongs to the insulin family. The insulin family, comprised of insulin, relaxin, insulin-like growth factors I and II ( IGF-I and IGF-II ), and possibly the beta-subunit of 7S nerve growth factor, represents a group of structurally related polypeptides whose biological functions have diverged. The IGFs, or somatomedins, constitute a class of polypeptides that have a key role in pre-adolescent mammalian growth. IGF-I expression is regulated by GH and mediates postnatal growth, while IGF-II appears to be induced by placental lactogen during prenatal development. IGF1 / IGF-I may be a physiological regulator of [1-14C]-2-deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblasts. IGF1 / IGF-I stimulates glucose transport in rat bone-derived osteoblastic (PyMS) cells and is effective at much lower concentrations than insulin, not only regarding glycogen and DNA synthesis but also about enhancing glucose uptake. Defects in IGF1 / IGF-I are the cause of insulin-like growth factor I deficiency (IGF1 deficiency) which is an autosomal recessive disorder characterized by growth retardation, sensorineural deafness, and mental retardation.

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