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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20℃
- 保质期:
12个月
- 英文名:
Recombinant V-Ki-Ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS)
- 库存:
1000
- 供应商:
上海信裕
| Organism species | Homo sapiens (Human) |
| Product No. | xy751Hu01 |
| Source | Prokaryotic expression |
| Host | E.coli |
| Purity | >95% |
| UOM | 50ug |
| Predicted Molecular Mass | 25.4kDa |
| Concentration | n/a |
| Applications | SDS-PAGE; WB; ELISA; IP. |
| Endotoxin Level | <1.0EU per 1µg (determined by the LAL method) |
| Formulation | Supplied as lyophilized form in PBS, pH7.4, containing 5% trehalose, 0.01% sarcosyl. |
MTEYKLVVVG AGGVGKSALT IQLIQNHFVD EYDPTIEDSY RKQVVIDGET CLLDILDTAG QEEYSAMRDQ YMRTGEGFLC VFAINNTKSF EDIHHYREQI KRVKDSEDVP MVLVGNKCDL PSRTVDTKQA QDLARSYGIP FIETSAKTRQ RVEDAFYTLV REIRQYRLKK ISKEEKTPGC VKIKKCIIM
Stability Test: The thermal stability is described by the loss rate of the target protein. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37oC for 48h, and no obvious degradation and precipitation were observed. (Referring from China Biological Products Standard, which was calculated by the Arrhenius equation.) The loss of this protein is less than 5% within the expiration date under appropriate storage condition.
Protein bands: 10kDa, 14kDa, 18kDa, 22kDa, 26kDa, 33kDa, 44kDa and 70kDa.
Double intensity bands: The 26kDa, 18kDa, 10kDa bands are at double intensity to make location and size approximation of proteins of interest quick and easy.
V-Ki-Ras2 Kirsten大鼠肉瘤病毒癌基因同源物(KRAS)重组蛋白Ready-to-use: No need to heat, dilute or add reducing agents before use.
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文献和实验Gln CAG Leu CTG K-ras-2来源的 正常人c-K-ras-2 人Caalu肺癌 人SW480结肠癌 鼠Kirsten病毒v-K-ras Gly Lys TGT Val GTT Ser Gly Ala Thr Gln N-ras来源的
正常,就可能导致细胞发生恶性转化。 表9-2 一些重要的癌基因 癌基因 来源 染色体定位 生化性质 信号传导蛋白 abl Abelson鼠白血病病毒 9q34 蛋白激酶 src 鸡Rous肉瘤病毒 20q12-13 蛋白激酶 trk 人大肠癌 1q32 蛋白激酶 H-ras Harvery大鼠肉瘤病毒 11p15.5 GTPase N-ras 各种人类肿瘤(如神经母细胞瘤) 1p13 GTPase 分泌生长因子 sis 猴肉瘤病毒 22q12.3-13
1179380155 请问能用ELISA(酶连接免疫吸附)法检测基因突变吗?感激不尽! woxingwosu ELISA-based Ki-ras gene mutation analyses in pancreatic and cholangiocarcinoma cells and tissues. Abstract Detection of Ki-ras mutations
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