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Merck
CN

F0291

Sigma-Aldrich

Fibroblast Growth Factor-Basic, human

≥97% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder, suitable for cell culture

别名:

成纤维细胞生长因子 7-碱性 人, FGF2, bFGF

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关于此项目

化学文摘社编号:
106096-93-9
MDL编号:
MFCD00081382
UNSPSC代码:
12352202
NACRES:
NA.77

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产品名称

hBFGF, FGF-Basic, recombinant, expressed in E. coli, suitable for cell culture

生物来源

human

质量水平

200

重组

expressed in E. coli

方案

≥97% (SDS-PAGE)

表单

lyophilized powder

效能

≤-0.6 ng/mL

分子量

16.0 kDa

包装

pkg of 4X25 μg
pkg of 25 μg

储存条件

avoid repeated freeze/thaw cycles

技术

cell culture | mammalian: suitable

杂质

≤1.00 EU/μg

颜色

white to faint yellow cast

溶解性

water: soluble 0.025 mg, clear, colorless to faintly yellow

UniProt登记号

P09038

储存温度

−20°C

基因信息

human ... FGF2 (2247)

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相关类别

一般描述

碱性成纤维细胞生长因子（FGF-Basic） 存在于基底膜和内皮下细胞外基质中。FGF-Basic 在胚胎发育早期被诱导，它是胚胎干细胞（ESC） 和谱系定义的干细胞的多能性和自我更新所必需的（但不充分）； 其中它起到支持增殖和抑制分化的作用。hESC 的自我更新取决于激活素/Nodal/Smad2,3 分支的激活和 TGFβ 家族细胞信号传导程序的 BMP/GDF/Smad5 分支的抑制。FGF-Basic 是多能性节点支持的感受态因子。FGF-Basic 是维持干细胞特性所必需且充分的。它诱导人 ES 细胞中 Nodal 和 FGF-Basic 的表达。

应用

碱性成纤维细胞生长因子（FGF-Basic）是维持培养物中人胚胎干细胞和各种其它干细胞系，如间充质干 （基质） 细胞 （MSC） 所必需的。

外形

从 20 mM Tris、1 M NaCl（pH 7.0，每1 μg BFGF含 50μg 牛血清白蛋白 (BSA)/1μg 脂联素）的 0.2 μm 过滤溶液冻干。

分析说明

FGF-Basic 的生物活性是在荧光测定中使用氧化还原敏感型染料刃天青进行测量。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

常规特殊物品
胰岛素激素类产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000451315
0000451315
0000195944
0000372843
0000355296

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R Beklem Bostancioglu et al.
Colloids and surfaces. B, Biointerfaces, 155, 415-428 (2017-05-02)
Accelerated Mesenchymal Stem Cells (MSCs) condensation and robust MSC-matrix and MSC-MSC interactions on nano-surfaces may provide critical factors contributing to such events, likely through the orchestrated signal cascades and cellular events modulated by the extracellular matrix. In this study, human
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Human embryonic stem cells (hESCs) self-renew indefinitely while maintaining pluripotency. The molecular mechanism underlying hESCs self-renewal and pluripotency is poorly understood. To identify the signaling pathway molecules that maintain the proliferation of hESCs, we performed a microarray analysis comparing an
C Xu et al.
Nature biotechnology, 19(10), 971-974 (2001-10-03)
Previous studies have shown that maintenance of undifferentiated human embryonic stem (hES) cells requires culture on mouse embryonic fibroblast (MEF) feeders. Here we demonstrate a successful feeder-free hES culture system in which undifferentiated cells can be maintained for at least
Brad Davidson et al.
Genes & development, 20(19), 2728-2738 (2006-10-04)
Comprehensive gene networks in Ciona intestinalis embryos provide a foundation for characterizing complex developmental processes, such as the initial phases of chordate heart development. The basic helix-loop-helix regulatory gene Ci-Mesp is required for activation of cardiac transcription factors. Evidence is
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