推荐产品
产品名称
抗-Raf-1抗体, Upstate®, from rabbit
生物来源
rabbit
质量水平
抗体形式
purified immunoglobulin
抗体产品类型
primary antibodies
克隆
polyclonal
种属反应性
human
制造商/商品名称
Upstate®
技术
immunoprecipitation (IP): suitable
western blot: suitable
同位素/亚型
IgG
NCBI登记号
UniProt登记号
运输
wet ice
靶向翻译后修饰
unmodified
基因信息
human ... RAF1(5894)
特异性
Raf-1
免疫原
对应于人 Raf-1 氨基酸 637-648 的肽。
应用
抗-Raf-1 抗体可检测Raf-1 水平 & 已发布 & 经过验证可用于IP & WB。
研究子类别
MAP激酶
MAP激酶
研究类别
信号传导
信号传导
质量
已通过免疫印迹法对3T3/A31细胞的RIPA裂解液进行了常规评估
目标描述
70kDa
联系
替代:04-412
外形
0.1M Tris-甘氨酸(pH 7.4),0.15M NaCl,0.05%叠氮化钠,然后添加甘油至30%
形式:纯化
纯化蛋白A
储存及稳定性
-20degC下保存2年
分析说明
对照
阳性抗原对照:货号12-305,3T3/A31裂解液。添加2.5 μL 2-巯基乙醇/100 μL裂解液,煮沸5分钟以还原 制剂。在微凝胶每个泳道上样20 μg经还原的裂解液。
阳性抗原对照:货号12-305,3T3/A31裂解液。添加2.5 μL 2-巯基乙醇/100 μL裂解液,煮沸5分钟以还原 制剂。在微凝胶每个泳道上样20 μg经还原的裂解液。
法律信息
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
免责声明
除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
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储存分类代码
10 - Combustible liquids
WGK
WGK 2
Dectin-1 directs T helper cell differentiation by controlling noncanonical NF-kappaB activation through Raf-1 and Syk.
Nature Immunology null
Cell death and differentiation, 13(11), 1982-1993 (2006-04-01)
Melanoma differentiation-associated gene-5 (mda-5) was the first molecule identified in nature whose encoded protein embodied the unique structural combination of an N-terminal caspase recruitment domain and a C-terminal DExD/H RNA helicase domain. As suggested by its structure, cumulative evidences documented
Journal of cellular and molecular medicine, 11(6), 1395-1407 (2008-01-22)
Mouse embryonic endothelial progenitor cells (eEPCs) acquire a mature phenotype after treatment with cyclic adenosine monophosphate (cAMP), suggesting an involvement of Raf serine/threonine kinases in the differentiation process. To test this idea, we investigated the role of B-Raf and C-Raf
Design and discovery of small molecules targeting raf-1 kinase.
Current Pharmaceutical Design, 8, 2269-2278 (2002)
The Journal of biological chemistry, 279(10), 9233-9247 (2003-12-13)
We have reported previously that protein kinase C (PKC) signaling can mediate a program of cell cycle withdrawal in IEC-18 nontransformed intestinal crypt cells, involving rapid disappearance of cyclin D1, increased expression of Cip/Kip cyclin-dependent kinase inhibitors, and activation of
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