这是一篇来自已证抗体库的有关Caenorhabd.. cnx-1的综述,是根据7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cnx-1 抗体。
Enzo Life Sciences
domestic rabbit 多克隆
  • 免疫印迹; 人类; 1:1000; 图 4a
Enzo Life Sciences cnx-1抗体(Enzo, ADI-SPA-865-D)被用于被用于免疫印迹在人类样本上浓度为1:1000 (图 4a). Acta Neuropathol Commun (2019) ncbi
domestic rabbit 多克隆
  • 免疫印迹; 人类; 1:5000; 图 2b
Enzo Life Sciences cnx-1抗体(Enzo Lifesciences, ADI-SPA-865)被用于被用于免疫印迹在人类样本上浓度为1:5000 (图 2b). Cell (2018) ncbi
domestic rabbit 多克隆
  • 免疫印迹; 大鼠; 图 1b
Enzo Life Sciences cnx-1抗体(Enzo Life Sciences, ADI-SPA-865)被用于被用于免疫印迹在大鼠样本上 (图 1b). Biochim Biophys Acta Mol Cell Biol Lipids (2018) ncbi
domestic rabbit 多克隆
  • 免疫印迹; 人类; 1:2000; 图 s8g
Enzo Life Sciences cnx-1抗体(Enzo, ADI-SPA-865)被用于被用于免疫印迹在人类样本上浓度为1:2000 (图 s8g). Nature (2017) ncbi
domestic rabbit 多克隆
  • 免疫印迹; 人类; 图 1b
Enzo Life Sciences cnx-1抗体(Enzo Life Sciences, ADI-SPA-865)被用于被用于免疫印迹在人类样本上 (图 1b). Biochem J (2016) ncbi
domestic rabbit 多克隆
  • 免疫印迹; 人类; 图 1b
Enzo Life Sciences cnx-1抗体(Enzo Life Sciences, ADI-SPA-865)被用于被用于免疫印迹在人类样本上 (图 1b). Biochem J (2016) ncbi
domestic rabbit 多克隆
  • 免疫组化; 人类; 1:300; 图 2d
Enzo Life Sciences cnx-1抗体(Enzo Life Sciences, ADI-SPA-865)被用于被用于免疫组化在人类样本上浓度为1:300 (图 2d). Nat Cell Biol (2016) ncbi
domestic rabbit 多克隆
  • 免疫组化; 人类; 1:300; 图 2d
Enzo Life Sciences cnx-1抗体(Enzo Life Sciences, ADI-SPA-865)被用于被用于免疫组化在人类样本上浓度为1:300 (图 2d). Nat Cell Biol (2016) ncbi
domestic rabbit 多克隆
  • 免疫印迹; 人类; 图 3
Enzo Life Sciences cnx-1抗体(stressgen, SPA-865)被用于被用于免疫印迹在人类样本上 (图 3). PLoS ONE (2016) ncbi
domestic rabbit 多克隆
  • 免疫印迹; 人类; 图 3
Enzo Life Sciences cnx-1抗体(stressgen, SPA-865)被用于被用于免疫印迹在人类样本上 (图 3). PLoS ONE (2016) ncbi
文章列表
  1. Gerber H, Mosser S, Boury Jamot B, Stumpe M, Piersigilli A, Goepfert C, et al. The APMAP interactome reveals new modulators of APP processing and beta-amyloid production that are altered in Alzheimer's disease. Acta Neuropathol Commun. 2019;7:13 pubmed 出版商
  2. Chitwood P, Juszkiewicz S, Guna A, Shao S, Hegde R. EMC Is Required to Initiate Accurate Membrane Protein Topogenesis. Cell. 2018;175:1507-1519.e16 pubmed 出版商
  3. Blunsom N, Gomez Espinosa E, Ashlin T, Cockcroft S. Mitochondrial CDP-diacylglycerol synthase activity is due to the peripheral protein, TAMM41 and not due to the integral membrane protein, CDP-diacylglycerol synthase 1. Biochim Biophys Acta Mol Cell Biol Lipids. 2018;1863:284-298 pubmed 出版商
  4. Keckesova Z, Donaher J, De Cock J, Freinkman E, Lingrell S, Bachovchin D, et al. LACTB is a tumour suppressor that modulates lipid metabolism and cell state. Nature. 2017;543:681-686 pubmed 出版商
  5. BRANDT C, McFie P, Stone S. Diacylglycerol acyltransferase-2 and monoacylglycerol acyltransferase-2 are ubiquitinated proteins that are degraded by the 26S proteasome. Biochem J. 2016;473:3621-3637 pubmed
  6. Schrul B, Kopito R. Peroxin-dependent targeting of a lipid-droplet-destined membrane protein to ER subdomains. Nat Cell Biol. 2016;18:740-51 pubmed 出版商
  7. Gerl M, Bittl V, Kirchner S, Sachsenheimer T, Brunner H, Lüchtenborg C, et al. Sphingosine-1-Phosphate Lyase Deficient Cells as a Tool to Study Protein Lipid Interactions. PLoS ONE. 2016;11:e0153009 pubmed 出版商