Human IGF1 Protein

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Human IGF1 Protein - SDS-PAGE电泳图
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货号: CY113
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产品名称 Human IGF1 Protein
中文名称 重组人胰岛素样生长因子1
种属 Human
表达宿主 E. coli
纯度 > 96 % as determined by SDS-PAGE
内毒素 < 1.0 EUper μg of the protein as determined by the LAL method.
生物活性 Measured in a cell proliferation assay using MCF-7 mouse embryonic fibroblasts. The ED50 for this effect is typically 0.2 ng/mL. The specific activity of recombinant Human IGF is approximately >5 x 106 IU/mg.
基因编号 3479
蛋白链接 https://www.uniprot.org/uniprotkb/P05019/entry
别名 Long R3 IGF-I;
蛋白序列 GPETLCGAELVDALQFVCGDRGFYFNKPTGYGSSSRRAPQTGIVDECCFRSCDLRRLEMYCAPLKPAKSA
蛋白标签 Tag free
预测分子量 The Recombinant Human IGF1 Protein consists of 71 amino acids and predicts a molecular mass of 7.8 Kda.
产品形式 Lyophilized from sterile 20 mM Tris with 150 mM NaCl, pH 7.4.
使用方式 Always centrifuge tubes before opening. It is recommended to reconstitute the lyophilized Human IGF1 Protein using the buffer we provided not less than 100µg/ml, which can then be further diluted to other aqueous solutions.
运输方式 The product is shipped at ambient temperature.
储存条件 Store at -20℃
产品背景 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.

*本产品仅供科研试验用,不可直接用于人体。

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