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当前位置: 首页 > 产品中心 > peptide > 细胞骨架/Ras G-LISA激活检测试剂盒(基于比色法)-96次检测/96次检测/BK131
商品详细细胞骨架/Ras G-LISA激活检测试剂盒(基于比色法)-96次检测/96次检测/BK131
细胞骨架/Ras G-LISA激活检测试剂盒(基于比色法)-96次检测/96次检测/BK131
细胞骨架/Ras G-LISA激活检测试剂盒(基于比色法)-96次检测/96次检测/BK131
商品编号: BK131
品牌: Cytoskeleton
市场价: ¥17400.00
美元价: 10440.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Details

Product Uses Include

  • Ras signaling pathway studies
  • Ras activation assays with primary cells
  • Studies of Ras activators and inactivators
  • Ras activation assays with limited material
  • High throughput screens for Ras activation

Introduction

With the new Ras G-LISA™ kit you can now measure Ras activation from cell and tissue samples in less than 3 h.  G-LISA™ requires only 1-5% of the material needed for a conventional pull-down assay.  You will also be able to handle large sample numbers and generate quantitative results.  For a more detailed introduction on G-LISA™ assays and a listing of other available G-LISA™ kits, see our main G-LISA™ page.

The Ras G-LISA™ kit contains a Ras GTP-binding protein linked to the wells of a 96 well plate. Active, GTP-bound Ras in cell/tissue lysates will bind to the wells while inactive GDP-bound Ras is removed during washing steps.  The bound active Ras is detected with a Ras specific antibody.  The degree of Ras activation is determined by comparing readings from activated cell lysates versus non-activated cell lysates.  Inactivation of Ras is generally achieved in tissue culture by a serum starvation step (see kit datasheet for more information).  

Kit contents

The kit contains sufficient reagents to perform 96 Ras activation assays. Since the Ras-GTP affinity wells are supplied as strips and the strips can be broken into smaller pieces, each kit can be used for anywhere from one to multiple assays. The following components are included in the kit: 

  1. 96 Ras-GTP affinity wells (divisible into 12 strips of 8 wells each)
  2. Lysis buffer
  3. Binding buffer
  4. Antigen presenting buffer
  5. Wash buffer
  6. Antibody dilution buffer
  7. Anti-Ras antibody
  8. HRP-labeled secondary antibody
  9. Positive control Ras protein
  10. Protease inhibitor cocktail (Cat. # PIC02)
  11. Absorbance detection reagents
  12. Precision Red™ Advanced protein assay reagent (Cat. # ADV02)
  13. Manual with detailed protocols and extensive troubleshooting guide

    Equipment needed

  14. 96-well plate spectrophotometer capable of reading 490 nm wavelength
  15. Multichannel or multidispensing pipettor
  16. Orbital microplate shaker capable of at least 200 rpm shaking (400 rpm is optimal)

Example results

BK131-Fig1

Figure 1.  Ras  activation by EGF measured by G-LISA™.  HeLa cells were serum starved (SS) for 24 h and treated with EGF (100 ng/ml for 2 min). 25,  12.5, 5, 1.25 µg of cell lysates were subjected to the G-LISA™ assay. Absorbance was read at 490 nm.  Data are background subtracted

Go to main G-LISA™ page

G-LISA Products:Cdc42 G-LISA™ Activation Assay, colorimetric format (Cat.# BK127)Rac1 G-LISA™ Activation Assay, luminescence format (Cat.# BK126)G-LISA Rac 1,2,3 Activation Assay Biochem Kit (colorimetric format (Cat.# BK125)RhoA G-LISA™ Activation Assay, colorimetric format (Cat.# BK124)RhoA G-LISA™ Activation Assay, luminescence format (Cat.# BK121)

Associated Products:Anti-Cdc42 monoclonal antibody (Cat.# ACD03)Anti-Rac1 monoclonal antibody (Cat.# ARC03)Anti-RhoA monoclonal antibody (Cat.# ARH03)

About

For product Datasheets and MSDSs please click on the PDF links below.   

  •  G-LISA Activation Assay Technical Guide download here
  •  G-LISA Data Analysis (Absorbance) Excel Template download here.

 

    Citations

    Wang, X., Yao, Y. & Gao, J. Sevoflurane inhibits growth factor-induced angiogenesis through suppressing Rac1/paxillin/FAK and Ras/Akt/mTOR. Futur. Oncol. 16, 1619–1627 (2020).

    Kim, J. H. et al. Rational design of small molecule RHOA inhibitors for gastric cancer. Pharmacogenomics J. 20, 601–612 (2020).

    Chen, G. P., Zhang, X. Q., Wu, T., Han, J. & Ye, D. Inhibition of farnesyl pyrophosphate synthase attenuates high glucose-induced vascular smooth muscle cells proliferation. Mol. Med. Rep. 15, 3153–3160 (2017).

    Lu, H. et al. Research paper resistance to allosteric SHP2 inhibition in FGFR-driven cancers through rapid feedback activation of FGFR. Oncotarget 11, 265–281 (2020).

    Casique-Aguirre, D. et al. KRas4B-PDE6δ complex stabilization by small molecules obtained by virtual screening affects Ras signaling in pancreatic cancer 06 Biological Sciences 0601 Biochemistry and Cell Biology. BMC Cancer 18, 1–16 (2018).

    Li, Q. fen, Decker-Rockefeller, B., Bajaj, A. & Pumiglia, K. Activation of Ras in the Vascular Endothelium Induces Brain Vascular Malformations and Hemorrhagic Stroke. Cell Rep. 24, 2869–2882 (2018).

    Zhao, T. et al. Simulated Microgravity Reduces Focal Adhesions and Alters Cytoskeleton and Nuclear Positioning Leading to Enhanced Apoptosis via Suppressing FAK/RhoA-Mediated mTORC1/NF-κB and ERK1/2 Pathways. Int. J. Mol. Sci. 19, 1994 (2018).

    S.-J. Lee et al. 2013. Regulation of hypoxia-inducible factor 1α (HIF-1α) by lysophosphatidic acid is dependent on interplay between p53 and krüppel-like factor 5. J. Biol. Chem. 288, 25244-25253.

    L.D. Camargo et al. 2013. Endo-PDI is required for TNFα-induced angiogenesis. Free Radic. Biol. Med. 65, 1398-1407.

    Gil-Henn et al. 2012. Arg/Abl2 promotes invasion and attenuates proliferation of breast cancer in vivo. Oncogene. doi:10.1038/onc.2012.284.

    Faqs

    Coming soon! If you have any questions concerning this product, please contact our Technical Service department at tservice@cytoskeleton.com

    品牌介绍
    Cytoskeleton,Inc.成立于1993年。自成立以来,我们一直在不断扩大产品范围。Cytoskeleton,Inc.很高兴为药物筛选,信号转导和细胞骨架研究提供广泛的试剂盒和产品。我们专注于纯化蛋白的生产和易于使用的试剂盒,以研究生化和细胞过程。我们的试剂盒既可用于基础研究或小型筛查的少量样品,也可用于大型筛查的高通量规模除了我们现有的产品外,我们还提供产品系列中微管,微管蛋白,运动蛋白,小G蛋白效应物,GAP,GEF和其他几种蛋白的药物筛选服务。有关更多信息,请参见我们的药物筛选服务页面。如果您想从市场上购买到特定产品,请随时与我们联系。我们在这里为您提供帮助。由于我们的科学家在各自的专业领域都有多年的工作经验,因此我们能够提供高质量的产品。自1993年成立以来,我们以合理的价格生产优质的产品而闻名。