- 询价
- 14-550
- 2025年07月16日
- Kinase Assay
- 0
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- 详细信息
- 文献和实验
- 技术资料
- 应用范围：
Kinase Assay
- 宿主：
0
- 抗原来源：
0
- 库存：
大量
- 是否单克隆：
0
- 规格：
10 μg
- Cardiovascular Disease
- Metabolic Disorders
- MAPK1
- p40
- PRKM2
- MAPK2
- PRKM1
- p42-MAPK
- p38
- p41
- ERK
- ERK-2
- ERT1
- P42MAPK
- p41mapk
- ERK2
更多产品技术资讯，请访问密理博中国博客：http://blog.milliporechina.com
详细描述见链接：http://www.millipore.com/catalogue/item/14-550
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文献和实验A Molecular Evolution Approach for Isolation of Intrinsically Active (MEK-Independent) MAP Kinases
on unconventional phosphorylation (on neighboring Thr + Tyr residues), a rational design of mutations that would render the kinase intrinsically active is currently unfeasible. Our method is based, therefore, on a “Molecular Evolution” approach that uses the power
MAP Kinase Activation by Receptor Tyrosine Kinases: In Control of Cell Migration
1/2 cascade. It has been shown that the ability of the ERK1/2 cascade to specify cell fate, such as cell migration, is dependent on signal duration governed by feedback control. Here we focus on one experimental system, MCF10A human mammary cells
Cell-Free Assay System for Ras- and Rap1-Dependent Activation of MAP-Kinase Cascade
It is well-established that Ras activates the mitogen-activated protein (MAP) kinase cascade consisting of MAP kinase, extracellular signal-regulated kinase (ERK), ERK kinase (MEK), and MEK kinase in mammals (for reviews, see refs. 1 –
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