产品编号:V7682查看说明书 产品名称:GTPase-Glo? Assay .0订购此产品 供应商:Promega 规格:10,000 Assays 目录价:18735 库存状态: CAS编号: 应用范围: 种属来源: 相关信息: 保存条件: 说明书地址:点击查看详细 打印此页关闭此页 上一个:GTPase-Glo? Assay[V7681/1,000 Assays] ...
Quantification of GTPase Cycling Rates of GTPases and GTPase:Effector Mixtures Using GTPase Glo Assaysdoi:10.1002/cpz1.1000Tschirpke, SophieDaalman, Werner K.‐G.Laan, LiedewijCurrent Protocols
2001. Expression, analysis, and properties of yeast ADP-ribosylation factor (ARF) of GTPase activating proteins (GAPs) Gcs1 and Glo3. Methods Enzymol. ... PP Poon,C Dan,I Huber,... - 《Methods in Enzymology》 被引量: 38发表: 2001年 Frequently Used Abbreviations : The Basque Phase of ...
The establishment of cell polarity is a prerequisite for many developmental processes. However, how it is achieved during tip growth in plants remains elusive. Here, we show that the RHO OF PLANTs (ROPs), ROP GUANINE NUCLEOTIDE EXCHANGE FACTORs (RopGEFs)
Four yeast proteins, Gcs1, Glo3, Age2, and Age1, have been shown to exert ArfGAP activity in vitro (8, 9, 10, 11), with the Age2 + Gcs1 ArfGAP pair providing essential overlapping function for post-Golgi transport (10). Vesicular transport is also mediated by membrane lipid ...
Using the GTPase-Glo Reagent, unhydrolized GTP is transformed into ATP. Subsequently, luciferase uses ATP as a substrate for the luciferin oxidation reaction, resulting in the bioluminescence effect. The intensity of luminescence is directly proportional to the amount of ATP. Thus, the luminescence ...
Bower, P. Gloviczki, D.V. Miller, D. Babovic-Vuksanovic, et al. Vascular abnormalities in patients with neurofibromatosis syndrome type I: clinical spectrum, management, and results J. Vasc. Surg., 46 (3) (2007), pp. 475-484 View in ScopusGoogle Scholar [6] J.M. Friedman, J. ...
Obesity and diabetes are well known risk factors for nonalcoholic fatty liver disease (NAFLD), but the genetic factors contributing to the development of NAFLD remain poorly understood. Here we describe two semi-dominant allelic missense mutations (Oily
Cytokine-dependent growth was determined by quantification of cellular ATP using the Cell Titer Glo Assay (Promega, Madison, WI, USA). Cells were washed with RPMI and starved for 3 hours in the presence of 1 mg/ml BSA. 3.75 × 104 cells/ml were seeded in a 96 well plate with the corr...
We show that the glo pathway functions downstream of rpm-1 and acts in parallel to fsn-1, a partner of RPM-1 E3 ligase function. We find that late endosomes are specifically disorganized at the presynaptic terminals of glo-4 mutants. Our data suggest that RPM-1 positively regulates a Rab...