产品简要
公司名称 :
赛信通(上海)生物试剂有限公司
产品类型 :
抗体
产品名称 :
Shh/Ihh Antibody
目录 :
2271
克隆性 :
多克隆
宿主 :
共轭标签 :
nonconjugated
反应物种 :
人类, 小鼠, 大鼠
应用 :
免疫印迹
文章摘录数: 29
出版应用/物种/样品/稀释参考文献
  • 免疫印迹; 人类; 图 4
Chen Y, Wei M, Wang C, Lee H, Pan S, Gao M, et al. Dual phosphoinositide 3-kinase/mammalian target of rapamycin inhibitor is an effective radiosensitizer for colorectal cancer. Cancer Lett. 2015;357:582-90 pubmed 出版商
Rodgers S, Ferguson D, Mitchell C, Ooms L. Regulation of PI3K effector signalling in cancer by the phosphoinositide phosphatases. Biosci Rep. 2017;37: pubmed 出版商
Amoroso M, Matassa D, Agliarulo I, Avolio R, Lu H, Sisinni L, et al. TRAP1 downregulation in human ovarian cancer enhances invasion and epithelial-mesenchymal transition. Cell Death Dis. 2016;7:e2522 pubmed 出版商
Yuan F, XU M, Li X, Xinlong H, Fang W, Dong J. The Roles of Acidosis in Osteoclast Biology. Front Physiol. 2016;7:222 pubmed 出版商
Chandra V, Karamitri A, Richards P, Cormier F, Ramond C, Jockers R, et al. Extracellular acidification stimulates GPR68 mediated IL-8 production in human pancreatic β cells. Sci Rep. 2016;6:25765 pubmed 出版商
Yu R, Yu B, Chen J, Lv X, Yan Z, Cheng Y, et al. Anti-tumor effects of Atractylenolide I on bladder cancer cells. J Exp Clin Cancer Res. 2016;35:40 pubmed 出版商
Wang H, Liu W, Black S, Turner O, Daniel J, Dean Colomb W, et al. Kaiso, a transcriptional repressor, promotes cell migration and invasion of prostate cancer cells through regulation of miR-31 expression. Oncotarget. 2016;7:5677-89 pubmed 出版商
Kong D, Li S, Du Z, Liu C, Liu B, Li C, et al. BAG3 elevation inhibits cell proliferation via direct interaction with G6PD in hepatocellular carcinomas. Oncotarget. 2016;7:700-11 pubmed 出版商
Tsurumaki H, Mogi C, Aoki Saito H, Tobo M, Kamide Y, Yatomi M, et al. Protective Role of Proton-Sensing TDAG8 in Lipopolysaccharide-Induced Acute Lung Injury. Int J Mol Sci. 2015;16:28931-42 pubmed 出版商
Qin H, Sha J, Jiang C, Gao X, Qu L, Yan H, et al. miR-122 inhibits metastasis and epithelial-mesenchymal transition of non-small-cell lung cancer cells. Onco Targets Ther. 2015;8:3175-84 pubmed 出版商
Liu M, Qi Z, Liu B, Ren Y, Li H, Yang G, et al. RY-2f, an isoflavone analog, overcomes cisplatin resistance to inhibit ovarian tumorigenesis via targeting the PI3K/AKT/mTOR signaling pathway. Oncotarget. 2015;6:25281-94 pubmed 出版商
Cohen Solal K, Boregowda R, Lasfar A. RUNX2 and the PI3K/AKT axis reciprocal activation as a driving force for tumor progression. Mol Cancer. 2015;14:137 pubmed 出版商
Tobo A, Tobo M, Nakakura T, Ebara M, Tomura H, Mogi C, et al. Characterization of Imidazopyridine Compounds as Negative Allosteric Modulators of Proton-Sensing GPR4 in Extracellular Acidification-Induced Responses. PLoS ONE. 2015;10:e0129334 pubmed 出版商
Yuan F, Zhao M, Jiang L, Wang H, Cao L, Zhou X, et al. Molecular actions of ovarian cancer G protein-coupled receptor 1 caused by extracellular acidification in bone. Int J Mol Sci. 2014;15:22365-73 pubmed 出版商
Park M, Kim B, Dong S, Lee S, Kim D, Rho S. The antihypertension drug doxazosin inhibits tumor growth and angiogenesis by decreasing VEGFR-2/Akt/mTOR signaling and VEGF and HIF-1? expression. Oncotarget. 2014;5:4935-44 pubmed
Ren W, Liu Y, Wan S, Fei C, Wang W, Chen Y, et al. BMP9 inhibits proliferation and metastasis of HER2-positive SK-BR-3 breast cancer cells through ERK1/2 and PI3K/AKT pathways. PLoS ONE. 2014;9:e96816 pubmed 出版商
Muniz Feliciano L, Van Grol J, Portillo J, Liew L, Liu B, Carlin C, et al. Toxoplasma gondii-induced activation of EGFR prevents autophagy protein-mediated killing of the parasite. PLoS Pathog. 2013;9:e1003809 pubmed 出版商
Song T, Wang L, Mo Z, Mao L, Ma X, Niu R, et al. Expression of p-Akt in ovarian serous carcinoma and its association with proliferation and apoptosis. Oncol Lett. 2014;7:59-64 pubmed
Juvin V, Malek M, Anderson K, Dion C, Chessa T, Lecureuil C, et al. Signaling via class IA Phosphoinositide 3-kinases (PI3K) in human, breast-derived cell lines. PLoS ONE. 2013;8:e75045 pubmed 出版商
Leal P, Garcia P, Sandoval A, Buchegger K, Weber H, Tapia O, et al. AKT/mTOR substrate P70S6K is frequently phosphorylated in gallbladder cancer tissue and cell lines. Onco Targets Ther. 2013;6:1373-84 pubmed 出版商
Dobbin Z, Landen C. The importance of the PI3K/AKT/MTOR pathway in the progression of ovarian cancer. Int J Mol Sci. 2013;14:8213-27 pubmed 出版商
De Marco C, Rinaldo N, Bruni P, Malzoni C, Zullo F, Fabiani F, et al. Multiple genetic alterations within the PI3K pathway are responsible for AKT activation in patients with ovarian carcinoma. PLoS ONE. 2013;8:e55362 pubmed 出版商
Lee H, Kim J, Kim E. Fucoidan from seaweed Fucus vesiculosus inhibits migration and invasion of human lung cancer cell via PI3K-Akt-mTOR pathways. PLoS ONE. 2012;7:e50624 pubmed 出版商
McCubrey J, Steelman L, Chappell W, Abrams S, Montalto G, Cervello M, et al. Mutations and deregulation of Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR cascades which alter therapy response. Oncotarget. 2012;3:954-87 pubmed
He J, Xu Q, Wang M, Li C, Qian X, Shi Z, et al. Oral administration of apigenin inhibits metastasis through AKT/P70S6K1/MMP-9 pathway in orthotopic ovarian tumor model. Int J Mol Sci. 2012;13:7271-82 pubmed 出版商
Virtakoivu R, Pellinen T, Rantala J, Perälä M, Ivaska J. Distinct roles of AKT isoforms in regulating ?1-integrin activity, migration, and invasion in prostate cancer. Mol Biol Cell. 2012;23:3357-69 pubmed 出版商
Saji M, Narahara K, McCarty S, Vasko V, La Perle K, Porter K, et al. Akt1 deficiency delays tumor progression, vascular invasion, and distant metastasis in a murine model of thyroid cancer. Oncogene. 2011;30:4307-15 pubmed 出版商
Kumar R, Blakemore S, Ellis C, Petricoin E, Pratt D, Macoritto M, et al. Causal reasoning identifies mechanisms of sensitivity for a novel AKT kinase inhibitor, GSK690693. BMC Genomics. 2010;11:419 pubmed 出版商
Smith D, Patel S, Raffoul F, Haller E, Mills G, Nanjundan M. Arsenic trioxide induces a beclin-1-independent autophagic pathway via modulation of SnoN/SkiL expression in ovarian carcinoma cells. Cell Death Differ. 2010;17:1867-81 pubmed 出版商
产品信息
SKU号 :
2271S
产品名称 :
Shh/Ihh Antibody
规格 :
100微升
Price-(USD) :
235美元
物种x :
M,(H, R)
应用 :
免疫印迹
产品种类 :
发育生物学
运输温度 :
AMBIENT
储存温度 :
-20°C
产品类型 :
多克隆抗体
分子量 :
19,(42, 45)
宿主 :
靶标 :
SHH
最初蛋白 :
SHH
别名 :
HHG-1,HHG1,HLP3,HPE3,MCOPCB5,SHH,SMMCI,Sonic hedgehog protein,Sonic hedgehog protein C-product,Sonic hedgehog protein N-product,TPT,TPTPS,sonic hedgehog homolog (Drosophila)
公司信息
赛信通(上海)生物试剂有限公司
上海市浦东南路1101号远东大厦514室,200120
info@cst-c.com.cn
www.cst-c.com.cn
2158356288
公司总部: 美国
赛信通生物试剂有限公司1999年成立于美国麻省,是一家私人拥有的公司,在全世界拥有超过400名员工。我们致力于提供用于帮助确定的细胞功能和抗病机制的创新型的研究工具。公司自成立以来,赛信通已成为全球领先的生产用于扩大细胞信号通路知识的最高质量的激活状态蛋白和总蛋白的抗体。我们的使命是为客户提供世界上最高质量的研究工具,以加快生物研究和个性化药物的进展。