这是一篇来自已证抗体库的有关人类 cdk7的综述,是根据44篇发表使用所有方法的文章归纳的。这综述旨在帮助来邦网的访客找到最适合cdk7 抗体。
cdk7 同义词: CAK; CAK1; CDKN7; HCAK; MO15; STK1; p39MO15; cyclin-dependent kinase 7; 39 KDa protein kinase; CDK-activating kinase 1; TFIIH basal transcription factor complex kinase subunit; cell division protein kinase 7; cyclin-dependent kinase 7 (MO15 homolog, Xenopus laevis, cdk-activating kinase); homolog of Xenopus MO15 Cdk-activating kinase; kinase subunit of CAK; serine/threonine kinase stk1; serine/threonine protein kinase 1; serine/threonine protein kinase MO15
赛默飞世尔
小鼠 单克隆(31TF2-1F8) | 赛默飞世尔 cdk7抗体(Affinity Bioreagent, MA3-001)被用于. PLoS ONE (2016) ncbi | |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity BioReagents, MA3-001)被用于被用于免疫印迹在Artemia franciscana样品上浓度为1:1250 (图 10). Integr Comp Biol (2005) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Acartia tonsa样品上浓度为1:2500 (图 7a). J Exp Mar Bio Ecol (2009) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity BioReagents, MA3-001)被用于被用于免疫印迹在面包酵母样品上浓度为1:2000 (图 3a). Cell Mol Biol Lett (2008) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Chinook salmon样品上浓度为1:500 (图 1a). Ecotoxicol Environ Saf (2009) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagent, MA3-001)被用于被用于免疫印迹在California mussel样品上 (图 2). Oecologia (2008) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity BioReagents, MA3-001)被用于被用于免疫印迹在Austrofundulus limnaeus样品上浓度为1:1000 (图 2a). Cell Stress Chaperones (2007) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Chinook salmon样品上浓度为1:500 (图 2). Environ Toxicol Chem (2007) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Balanus glandula样品上浓度为1:2500 (图 1). Biol Bull (2007) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity BioReagents, MA3-001)被用于被用于免疫印迹在Artemia franciscana样品上浓度为1:1250 (图 4). Comp Biochem Physiol B Biochem Mol Biol (2006) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在long-jawed mudsucker样品上浓度为1:2500. Comp Biochem Physiol A Mol Integr Physiol (2006) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在bay mussel样品上浓度为1:500 (图 2). Biomarkers (2005) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Maori chief样品上 (图 1b) 和 被用于免疫印迹在emerald rockcod样品上 (图 1b). Cell Stress Chaperones (2005) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在猪样品上浓度为1:1000 (图 1). Toxicol Lett (2005) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagent, MA3-001)被用于被用于免疫印迹在牛样品上 (图 1d), 被用于免疫印迹在emerald rockcod样品上 (图 1d), 被用于免疫印迹在Notocypraea angustata样品上 (图 1d) 和 被用于免疫印迹在bald rockcod样品上 (图 1d). Am J Physiol Regul Integr Comp Physiol (2005) ncbi |
小鼠 单克隆(31TF2-1F8) | 赛默飞世尔 cdk7抗体(Affinity BioReagents, MA3-001)被用于. J Biosci (2004) ncbi | |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Sacramento splittail样品上浓度为1:500 (图 4a). Mar Environ Res (2005) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在long-jawed mudsucker样品上浓度为1:2500. Physiol Biochem Zool (2004) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Chinook salmon样品上浓度为1:500 (图 1). Mar Environ Res (2004) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Corbula amurensis样品上浓度为1:500 (图 1). Mar Environ Res (2004) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Macoma nasuta样品上浓度为1:500 (表 1). Mar Environ Res (2004) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity BioReagent, MA3-001)被用于被用于免疫印迹在brown tegula样品上 (图 1b). Biol Bull (2003) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Pacific oyster样品上 (图 4). Biol Bull (2003) ncbi |
小鼠 单克隆(31TF2-1F8) | 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于. Mar Environ Res (2002) ncbi | |
小鼠 单克隆(31TF2-1F8) | 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于. J Exp Biol (2002) ncbi | |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫细胞化学在African green monkey样品上 (图 2a). J Virol (2002) ncbi |
小鼠 单克隆(31TF2-1F8) | 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于. J Exp Biol (2002) ncbi | |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在Artemia franciscana样品上浓度为1:1250 (图 3). J Cell Biochem (2002) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在California mussel样品上 (图 7). Biol Bull (2001) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在bay mussel样品上 (图 4). J Exp Biol (2001) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在long-jawed mudsucker样品上 (图 2b). J Exp Biol (2001) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Anity Bioreagents, MA3-001)被用于被用于免疫印迹在Corbula amurensis样品上浓度为1:500 (图 2). Mar Environ Res (2000) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫组化在Corbula amurensis样品上 (图 2). Mar Environ Res (2000) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在green sea urchin样品上 (图 6). J Exp Zool (2001) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity BioReagents, MA3-001)被用于被用于免疫印迹在Artemia franciscana样品上 (图 10). Cell Tissue Res (2000) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity BioReagents, MA3-001)被用于被用于免疫印迹在emerald rockcod样品上 (图 4). J Exp Biol (2000) ncbi |
小鼠 单克隆(31TF2-1F8) |
| 赛默飞世尔 cdk7抗体(Affinity Bioreagents, MA3-001)被用于被用于免疫印迹在emerald rockcod样品上 (图 2). Comp Biochem Physiol A Mol Integr Physiol (2000) ncbi |
圣克鲁斯生物技术
小鼠 单克隆(C-4) |
| 圣克鲁斯生物技术 cdk7抗体(Santa Cruz, SC-7344)被用于被用于免疫沉淀在人类样品上 (图 4b). Nat Commun (2017) ncbi |
小鼠 单克隆(C-4) |
| 圣克鲁斯生物技术 cdk7抗体(Santa Cruz, C-4)被用于被用于免疫印迹在人类样品上 (图 3a). J Virol (2016) ncbi |
小鼠 单克隆(MO-1) |
| 圣克鲁斯生物技术 cdk7抗体(SCBT, MO-1)被用于被用于其他在人类样品上 (图 st1). Mol Cell Proteomics (2016) ncbi |
小鼠 单克隆(C-5) |
| 圣克鲁斯生物技术 cdk7抗体(Santa, sc-365075)被用于被用于免疫印迹在小鼠样品上 (图 s1h) 和 被用于免疫印迹在人类样品上 (图 s1h). Cell (2014) ncbi |
小鼠 单克隆(C-4) |
| 圣克鲁斯生物技术 cdk7抗体(Santa, sc-7344)被用于被用于免疫沉淀在人类样品上 和 被用于免疫印迹在人类样品上. Mol Cell Biol (2014) ncbi |
艾博抗(上海)贸易有限公司
兔 多克隆 |
| 艾博抗(上海)贸易有限公司 cdk7抗体(Abcam, ab59987)被用于被用于免疫印迹在人类样品上 (图 s2b). Cell (2014) ncbi |
赛信通(上海)生物试剂有限公司
小鼠 单克隆(MO1) |
| 赛信通(上海)生物试剂有限公司 cdk7抗体(Cell Signaling, 2916P)被用于被用于免疫印迹在人类样品上 (图 1c). Mol Cell (2017) ncbi |
小鼠 单克隆(MO1) |
| 赛信通(上海)生物试剂有限公司 cdk7抗体(Cell Signaling, MO1)被用于被用于免疫印迹在人类样品上. J Virol (2014) ncbi |
文章列表
- Kelso T, Baumgart K, Eickhoff J, Albert T, Antrecht C, Lemcke S, et al. Cyclin-dependent kinase 7 controls mRNA synthesis by affecting stability of preinitiation complexes, leading to altered gene expression, cell cycle progression, and survival of tumor cells. Mol Cell Biol. 2014;34:3675-88 pubmed 出版商
- Tartarotti B, Torres J. Sublethal stress: Impact of solar UV radiation on protein synthesis in the copepod Acartia tonsa. J Exp Mar Bio Ecol. 2009;375:106-113 pubmed
- Podrabsky J, Somero G. An inducible 70 kDa-class heat shock protein is constitutively expressed during early development and diapause in the annual killifish Austrofundulus limnaeus. Cell Stress Chaperones. 2007;12:199-204 pubmed
- Eder K, Köhler H, Werner I. Pesticide and pathogen: heat shock protein expression and acetylcholinesterase inhibition in juvenile Chinook salmon in response to multiple stressors. Environ Toxicol Chem. 2007;26:1233-42 pubmed
- Berger M, Emlet R. Heat-shock response of the upper intertidal barnacle Balanus glandula: thermal stress and acclimation. Biol Bull. 2007;212:232-41 pubmed
- Clegg J, Campagna V. Comparisons of stress proteins and soluble carbohydrate in encysted embryos of Artemia franciscana and two species of Parartemia. Comp Biochem Physiol B Biochem Mol Biol. 2006;145:119-25 pubmed
- Lund S, Ruberté M, Hofmann G. Turning up the heat: the effects of thermal acclimation on the kinetics of hsp70 gene expression in the eurythermal goby, Gillichthys mirabilis. Comp Biochem Physiol A Mol Integr Physiol. 2006;143:435-46 pubmed
- La Porte P. Mytilus trossulus hsp70 as a biomarker for arsenic exposure in the marine environment: laboratory and real-world results. Biomarkers. 2005;10:417-28 pubmed
- Place S, Hofmann G. Temperature differentially affects adenosine triphosphatase activity in Hsc70 orthologs from Antarctic and New Zealand notothenioid fishes. Cell Stress Chaperones. 2005;10:104-13 pubmed
- Ryan P, Bedard K, Breining T, Cribb A. Disruption of the endoplasmic reticulum by cytotoxins in LLC-PK1 cells. Toxicol Lett. 2005;159:154-63 pubmed
- Place S, Hofmann G. Comparison of Hsc70 orthologs from polar and temperate notothenioid fishes: differences in prevention of aggregation and refolding of denatured proteins. Am J Physiol Regul Integr Comp Physiol. 2005;288:R1195-202 pubmed
- Tanguay J, Reyes R, Clegg J. Habitat diversity and adaptation to environmental stress in encysted embryos of the crustacean Artemia. J Biosci. 2004;29:489-501 pubmed
- Teh S, Deng D, Werner I, Teh F, Hung S. Sublethal toxicity of orchard stormwater runoff in Sacramento splittail (Pogonichthys macrolepidotus) larvae. Mar Environ Res. 2005;59:203-16 pubmed
- Buckley B, Hofmann G. Magnitude and duration of thermal stress determine kinetics of hsp gene regulation in the goby Gillichthys mirabilis. Physiol Biochem Zool. 2004;77:570-81 pubmed
- Eder K, Leutenegger C, Wilson B, Werner I. Molecular and cellular biomarker responses to pesticide exposure in juvenile chinook salmon (Oncorhynchus tshawytscha). Mar Environ Res. 2004;58:809-13 pubmed
- Werner I. The influence of salinity on the heat-shock protein response of Potamocorbula amurensis (Bivalvia). Mar Environ Res. 2004;58:803-7 pubmed
- Werner I, Teh S, Datta S, Lu X, Young T. Biomarker responses in Macoma nasuta (Bivalvia) exposed to sediments from northern San Francisco Bay. Mar Environ Res. 2004;58:299-304 pubmed
- Tomanek L, Sanford E. Heat-shock protein 70 (Hsp70) as a biochemical stress indicator: an experimental field test in two congeneric intertidal gastropods (genus: Tegula). Biol Bull. 2003;205:276-84 pubmed
- Hamdoun A, Cheney D, Cherr G. Phenotypic plasticity of HSP70 and HSP70 gene expression in the Pacific oyster (Crassostrea gigas): implications for thermal limits and induction of thermal tolerance. Biol Bull. 2003;205:160-9 pubmed
- Werner I, Geist J, Okihiro M, Rosenkranz P, Hinton D. Effects of dietary exposure to the pyrethroid pesticide esfenvalerate on medaka (Oryzias latipes). Mar Environ Res. 2002;54:609-14 pubmed
- Buckley B, Hofmann G. Thermal acclimation changes DNA-binding activity of heat shock factor 1 (HSF1) in the goby Gillichthys mirabilis: implications for plasticity in the heat-shock response in natural populations. J Exp Biol. 2002;205:3231-40 pubmed
- Guerrero C, Bouyssounade D, Zárate S, Isa P, López T, Espinosa R, et al. Heat shock cognate protein 70 is involved in rotavirus cell entry. J Virol. 2002;76:4096-102 pubmed
- Tomanek L, Somero G. Interspecific- and acclimation-induced variation in levels of heat-shock proteins 70 (hsp70) and 90 (hsp90) and heat-shock transcription factor-1 (HSF1) in congeneric marine snails (genus Tegula): implications for regulation of hsp gene expression. J Exp Biol. 2002;205:677-85 pubmed
- Willsie J, Clegg J. Small heat shock protein p26 associates with nuclear lamins and HSP70 in nuclei and nuclear matrix fractions from stressed cells. J Cell Biochem. 2002;84:601-14 pubmed
- Helmuth B, Hofmann G. Microhabitats, thermal heterogeneity, and patterns of physiological stress in the rocky intertidal zone. Biol Bull. 2001;201:374-84 pubmed
- Buckley B, Owen M, Hofmann G. Adjusting the thermostat: the threshold induction temperature for the heat-shock response in intertidal mussels (genus Mytilus) changes as a function of thermal history. J Exp Biol. 2001;204:3571-9 pubmed
- Place S, Hofmann G. Temperature interactions of the molecular chaperone Hsc70 from the eurythermal marine goby Gillichthys mirabilis. J Exp Biol. 2001;204:2675-82 pubmed
- Werner I, Hinton D. Spatial profiles of hsp70 proteins in Asian clam (Potamocorbula amurensis) in northern San Francisco Bay may be linked to natural rather than anthropogenic stressors. Mar Environ Res. 2000;50:379-84 pubmed
- Teh S, Werner I, Hinton D. Sublethal effects of chromium-VI in the Asian clam (Potamocorbula amurensis). Mar Environ Res. 2000;50:295-300 pubmed
- Stephens R. Ciliary protein turnover continues in the presence of inhibitors of golgi function: evidence for membrane protein pools and unconventional intracellular membrane dynamics. J Exp Zool. 2001;289:335-49 pubmed
- Clegg J, Jackson S, Popov V. Long-term anoxia in encysted embryos of the crustacean, Artemia franciscana: viability, ultrastructure, and stress proteins. Cell Tissue Res. 2000;301:433-46 pubmed
- Hofmann G, Buckley B, Airaksinen S, Keen J, Somero G. Heat-shock protein expression is absent in the antarctic fish Trematomus bernacchii (family Nototheniidae). J Exp Biol. 2000;203:2331-9 pubmed
- Carpenter C, Hofmann G. Expression of 70 kDa heat shock proteins in antarctic and New Zealand notothenioid fish. Comp Biochem Physiol A Mol Integr Physiol. 2000;125:229-38 pubmed