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生物源
mouse
共軛
unconjugated
抗體表格
purified immunoglobulin
抗體產品種類
primary antibodies
無性繁殖
3B10-2F2, monoclonal
形狀
buffered aqueous solution
物種活性
human
技術
ELISA: suitable
capture ELISA: suitable
immunofluorescence: suitable
western blot: 1-5 μg/mL
同型
IgG1κ
GenBank登錄號
UniProt登錄號
應用
research pathology
運輸包裝
dry ice
儲存溫度
−20°C
目標翻譯後修改
unmodified
基因資訊
human ... KRAS(3845)
一般說明
Kirsten大鼠肉瘤病毒癌基因同源物（KRAS）是癌基因，映射至人12p12.1染色体。选择性剪接产生编码两个同工型变体，在C末端区域不同。该基因编码小GTP酶超家族的成员。
免疫原
KRAS (AAH13572，1 a.a.~188 a.a) 带有 GST 标签的全长重组蛋白。仅 GST 标签的分子量为 26 kDa。
序列
MTEYKLVVVGAGGVGKSALTIQLIQNHFVDEYDPTIEDSYRKQVVIDGETCLLDILDTAGHEEYSAMRDQYMRTGEGFLCVFAINNTKSFEDIHHYREQIKRVKDSEDVPMVLVGNKCDLPSRTVDTKQAQDLARSYGIPFIETSAKTRQGVDDAFYTLVREIRKHKEKMSKDGKKKKKKSKTKCVIM
序列
MTEYKLVVVGAGGVGKSALTIQLIQNHFVDEYDPTIEDSYRKQVVIDGETCLLDILDTAGHEEYSAMRDQYMRTGEGFLCVFAINNTKSFEDIHHYREQIKRVKDSEDVPMVLVGNKCDLPSRTVDTKQAQDLARSYGIPFIETSAKTRQGVDDAFYTLVREIRKHKEKMSKDGKKKKKKSKTKCVIM
應用
小鼠抗 KRAS 单克隆抗体用于：免疫沉淀、免疫荧光、蛋白质印迹、 间接酶联免疫吸附测定（ELISA）。
生化／生理作用
Kirsten大鼠肉瘤病毒致癌基因同源物（KRAS）是Ras信号通路的关键蛋白。促进肿瘤侵袭和转移。该基因的功能获得性突变致使多种肿瘤发生，包括胰腺肿瘤、胆道肿瘤和结肠肿瘤。这种突变在胃癌中很少见到。
外觀
磷酸盐缓冲盐溶液，pH 7.4
法律資訊
GenBank is a registered trademark of United States Department of Health and Human Services
免責聲明
除非我们的产品目录或产品随附的其他公司文件中另有说明，否则我们的产品仅用于研究用途，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、体外或体内治疗用途或任何类型的人类或动物消费或应用。
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儲存類別代碼
10 - Combustible liquids
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
其他客户在看
Loss of heterozygosity of chromosome 12p does not correlate with KRAS mutation in non-small cell lung cancer
Uchiyama M, et al.
International Journal of Cancer. Journal International Du Cancer, 107, 962-969 (2003)
Noise-reducing optogenetic negative-feedback gene circuits in human cells
Guinn MT, et al.
Nucleic Acids Research, 47, 7703-7714 (2019)
Michael Tyler Guinn et al.
Nucleic acids research, 47(14), 7703-7714 (2019-07-04)
Gene autorepression is widely present in nature and is also employed in synthetic biology, partly to reduce gene expression noise in cells. Optogenetic systems have recently been developed for controlling gene expression levels in mammalian cells, but most have utilized
A novel method, digital genome scanning detects KRAS gene amplification in gastric cancers: involvement of overexpressed wild-type KRAS in downstream signaling and cancer cell growth
Mita H, et al.
BMC Cancer, 9, 1-16 (2009)
Eusebio Manchado et al.
Nature, 534(7609), 647-651 (2016-06-25)
Therapeutic targeting of KRAS-mutant lung adenocarcinoma represents a major goal of clinical oncology. KRAS itself has proved difficult to inhibit, and the effectiveness of agents that target key KRAS effectors has been thwarted by activation of compensatory or parallel pathways
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