武汉费斯德生物科技有限公司, NewEast Biosciences 中国办事处
武汉费斯德生物科技有限公司是美国NewEast Biosciences在中国的办事处。NewEast Biosciences 在十二年前率先研发俩种独特的抗体。这俩种抗体仅仅识别活性的GTP酶或者突变的Oncogene。 GTP酶涉及(1)响应细胞表面受体激活的信号转导,包括跨膜受体,例如介导味觉、嗅觉和视觉的那些,(2)核糖体的蛋白质生物合成,(3)调节细胞分化、增殖、分裂和运动,(4)蛋白质通过膜的易位,(5)细胞内囊泡的运输,以及囊泡介导的分泌和摄取,通过GTP酶控制囊泡外壳组装。Oncogene侧是诱发癌症的基因。
我公司将向你提供以下的独一无二的三种抗体或者试剂盒: (1) 仅识别 GTP酶的活性构型的产品, 它可以让你能够量化GTP酶在细胞中的活性和分布。(2) 识别突变 Oncogene蛋白, 但不认识相应野生型的抗体。 (3) 对 cAMP 和 cGMP 具有超亲和力(无需乙酰化)ELISA检测试剂盒。这些产品被将近一千篇同行评议的文章所引用。
¥347.00
产品名称: Rap1B 蛋白 |
货号 10120 |
产品全名: Rap1B 蛋白 |
基因符号 Member of RAS oncogene family, K-REV, RAL1B |
Source: Human, recombinant full length, His6-tag |
Expression 种属反应性: E. coli |
分子量: 21 kDa |
纯化: >95% by SDS-PAGE |
Introduction: Small GTPases are a super-family of cellular signaling regulators. Rap family members (Rap1A, Rap1B, Rap2A, Rap2B, and Rap2C) are Ras-like GTPases that regulate cell proliferation, differentiation, apoptosis and adhesion mechanisms. Rap1 (Ras-proximate-1) regulates apoptosis through interaction with two MAP3K effectors of the MEK/ERK MAP-kinase pathway. |
Amino Acid Sequence (1-184) |
MREYKLVVLGSGGVGKSALTVQFVQGIFVEKYDPTIEDSYRKQVEVDAQQCMLEILDTAGTEQFTAM RDLYMKNGQGFALVYSITAQSTFNDLQDLREQILRVKDTDDVPMILVGNKCDLEDERVVGKEQGQNL ARQWNNCAFLESSAKSKINVNEIFYDLVRQINRKTPVPGKARKKSSCQLL |
Properties |
Physical Appearance (form): Dissolved in 20mM Tris-HCl, pH8.0, 150mM NaCl. |
Physical Appearance (form): White or clear |
Concentration: 1 mg/mL |
Storage: -80°C |
Preparation Instructions: Centrifuge the vial before open the cap and reconstitute in water. Adding of 10 mM β-mercaptoethanol or 1 mM DTT into the solution to protect the protein is recommended and using of non-ionic detergents such as n-Dodecyl β-D-maltoside (DoDM) or polyethylene detergents (e.g. C12E10) also help to stabilize the protein. Avoid repeated freezing and thawing after reconstitution. The purity of His-tagged Rap1B was determined by SDS- PAGE and Coomassie Brilliant Blue Staining |
References:
1. hrzanowska-Wodnicka, M. et al., J. Clin. Invest. 115: 680-687, 2005.
2. Hoshijima, M. et al., Biochem. Biophys. Res. Commun. 157: 851-860, 1988.
3. Kawata, M. et al., Proc. Nat. Acad. Sci. 87: 8960-8964, 1990.
4. Kawata, M. et al., J. Biol. Chem. 264: 15688-15695, 1989.
5. Lova, P. et al., J. Biol. Chem. 278: 131-138, 2003.
6. Matsui, Y. et al., Biochem. Biophys. Res. Commun. 166: 1010-1016, 1990.
7. Pizon, V. et al., Nucleic Acids Res. 16: 7719-only, 1988.
8. Rehmann, H. et al., Nature 455: 124-127, 2008.
9. Rousseau-Merck, M. F. et al., Cytogenet. Cell Genet. 53: 2-4, 1990.
10. Schwamborn, J. C. et al., Nature Neurosci. 7: 923-929, 2004.