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當(dāng)前位置:首頁(yè)產(chǎn)品中心細(xì)胞因子及蛋白細(xì)胞因子PRP1955-50 μg重組人胰島素樣生長(zhǎng)因子1

重組人胰島素樣生長(zhǎng)因子1
產(chǎn)品簡(jiǎn)介:

Abbkine/亞科因重組人胰島素樣生長(zhǎng)因子1通過(guò)LAL法測(cè)定,每微克蛋白里內(nèi)毒素含量<1.0 EU。

產(chǎn)品型號(hào):PRP1955-50 μg

更新時(shí)間:2025-12-23

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品牌Abbkine/亞科因
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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