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Precision Plus ProteinTM KaleidoscopeTM Prestained Protein Standards

Precision Plus蛋白TM Kaleidoscope TM预染蛋白标准品

Company: Bio-Rad Laboratories
Catalog#: 1610375
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Deoxycholate Fractionation of Fibronectin (FN) and Biotinylation Assay to Measure Recycled FN Fibrils in Epithelial Cells
Author:
Date:
2018-08-20
[Abstract]  Fibronectin (FN) is an extracellular matrix protein that is secreted by many cell types and binds predominantly to the cell surface receptor Integrin α5β1. Integrin α5β1 binding initiates the step-wise assembly of FN into fibrils, a process called fibrillogenesis. We and several others have demonstrated critical effects of fibrillogenesis on cell migration and metastasis. While immunostaining and microscopy methods help visualize FN incorporation into fibrils, with each fibril being at least 3 μm in length, the first study that developed a method to biochemically fractionate FN to quantify fibril incorporated FN was published by Jean Schwarzbauer’s group in 1996. Our protocol was adapted from the original publication, and has been tested on multiple cell types including as shown here in ... [摘要]  纤连蛋白(FN)是一种细胞外基质蛋白,由许多细胞类型分泌,主要与细胞表面受体整合素α5β1结合。整合素α5β1结合启动FN逐步组装成原纤维,这一过程称为原纤维形成。我们和其他几个人已经证明了原纤维形成对细胞迁移和转移的关键作用。虽然免疫染色和显微镜方法有助于可视化FN掺入原纤维,每个原纤维的长度至少为3μm,但是第一项研究开发了一种生物化学分离FN以量化原纤维并入FN的方法,由Jean Schwarzbauer小组于1996年出版。我们的方案改编自原始出版物,并已在多种细胞类型上进行测试,包括如此处所示的MCF10A乳腺上皮细胞和Caki-1肾癌上皮细胞。使用两种洗涤剂提取物,将细胞FN分离成不溶于洗涤剂或掺入原纤维的FN和可溶性FN或未掺入的级分。为了确定原纤维形成是否利用FN的再循环池,我们使用了生物素标记的FN(FN-生物素)再循环测定,其已经从先前的研究中修改。使用再循环测定和脱氧胆酸盐分离方法的组合,可以定量地证明在不同实验条件下细胞中原纤维形成的程度,并确定原纤维形成的FN来源

【背景】 纤连蛋白(FN)是普遍产生的细胞外基质(ECM)组分(Uitto et al。,1989; Mao和Schwarzbauer,2005)。纤连蛋白库是转录产生的,可以通过几种生长因子如TGF-β1增加(Yokoi et al。,2002; Mimura ...

TGFβ Stimulation Assay
Author:
Date:
2014-12-05
[Abstract]  TGFβ is part of a growth factor superfamily which modulates cell growth, differentiation, adhesion, migration, ECM synthesis and apoptosis (Massague, 1998; Siegel and Massague, 2003). Free TGFβ binds to its high affinity TGFβ receptor, a receptor serine/threonine kinase, inducing phosphorylation of Smad2/3 which subsequently forms a complex with Smad4 to translocate to the nucleus where it interacts with multiple co-activators and repressors generating distinct transcriptional responses.

Indeed, TGFβ signaling shows a remarkable cellular context dependency and apparent multifunctionality: e.g. TGFβ is able to inhibit cell proliferation in many epithelial cells but can also enhance proliferation in fibroblasts and cell growth in endothelial cells (Guasch et al., ...
[摘要]  TGFβ是调节细胞生长,分化,粘附,迁移,ECM合成和凋亡的生长因子超家族的一部分(Massague,1998; Siegel和Massague,2003)。游离TGFβ结合到其高亲和力TGFβ受体,一种受体丝氨酸/苏氨酸激酶,诱导Smad2/3的磷酸化,随后与Smad4形成复合物转移到细胞核,其中它与多种共激活剂和阻遏物相互作用产生不同的转录反应。实际上,TGFβ信号传导显示出显着的细胞环境依赖性和表观多功能性:例如TGFβ能够抑制许多上皮细胞中的细胞增殖,但也可以增强成纤维细胞中的增殖和内皮细胞中的细胞生长(Guasch等人,2007; Xiao等人,2012年);它增强干细胞多能性,但促进其他细胞的分化(Park,2011);在癌症发展中,它抑制恶变前细胞增殖,但同时促进转移到转移表型(Chaudhury和Howe,2009)。
TGFβ刺激测定监测细胞对TGFβ的反应性。在TGFβ刺激时,可以分析短期效应例如Smad2磷酸化和长期效应例如细胞增殖。将描述用于小鼠角质形成细胞的测定,其中TGFβ强烈抑制细胞增殖,但是这两种测定也适用于其它细胞类型。

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