这是一篇来自已证抗体库的有关人类 CACNA1S的综述,是根据16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CACNA1S 抗体。
CACNA1S 同义词: CACNL1A3; CCHL1A3; Cav1.1; HOKPP; HOKPP1; MHS5; TTPP1; hypoPP; voltage-dependent L-type calcium channel subunit alpha-1S; calcium channel, L type, alpha 1 polypeptide, isoform 3 (skeletal muscle, hypokalemic periodic paralysis); calcium channel, voltage-dependent, L type, alpha 1S subunit; dihydropyridine receptor alpha 1 subunit; dihydropyridine-sensitive L-type calcium channel alpha-1 subunit; voltage-gated calcium channel subunit alpha Cav1.1

赛默飞世尔
小鼠 单克隆(1A)
  • 免疫印迹; 小鼠; 1:1000; 图 s2f
赛默飞世尔 CACNA1S抗体(Thermo Scientific, MA3-920)被用于被用于免疫印迹在小鼠样本上浓度为1:1000 (图 s2f). Nat Commun (2017) ncbi
小鼠 单克隆(1A)
  • 免疫印迹; 人类; 1:2000; 图 1b
赛默飞世尔 CACNA1S抗体(Thermo Fischer, MA3-920)被用于被用于免疫印迹在人类样本上浓度为1:2000 (图 1b). Acta Neuropathol Commun (2017) ncbi
小鼠 单克隆(1A)
  • 免疫印迹; 小鼠; 图 2e
赛默飞世尔 CACNA1S抗体(Pierce Antibodies, MA3-920)被用于被用于免疫印迹在小鼠样本上 (图 2e). PLoS ONE (2017) ncbi
小鼠 单克隆(1A)
  • 免疫组化; 斑马鱼; 1:100; 图 1a
赛默飞世尔 CACNA1S抗体(Thermo, MA3-920)被用于被用于免疫组化在斑马鱼样本上浓度为1:100 (图 1a). Proc Natl Acad Sci U S A (2017) ncbi
小鼠 单克隆(1A)
  • 免疫印迹; 大鼠; 1:1000; 图 5a
赛默飞世尔 CACNA1S抗体(ThermoFisher Scientific, MA3-920)被用于被用于免疫印迹在大鼠样本上浓度为1:1000 (图 5a). J Appl Physiol (1985) (2017) ncbi
小鼠 单克隆(1A)
  • 免疫印迹; 小鼠; 1:1000; 图 6
赛默飞世尔 CACNA1S抗体(Thermo Fisher Scientific, MA3-920)被用于被用于免疫印迹在小鼠样本上浓度为1:1000 (图 6). elife (2016) ncbi
小鼠 单克隆(1A)
  • 免疫印迹; 小鼠; 图 13
赛默飞世尔 CACNA1S抗体(ThermoFisher Scientific, 1A)被用于被用于免疫印迹在小鼠样本上 (图 13). Skelet Muscle (2016) ncbi
小鼠 单克隆(1A)
  • 免疫印迹; 小鼠; 1:1000; 图 5, 6
赛默飞世尔 CACNA1S抗体(Pierce, MA3-920)被用于被用于免疫印迹在小鼠样本上浓度为1:1000 (图 5, 6). Hum Mol Genet (2016) ncbi
小鼠 单克隆(1A)
  • 免疫组化; 小鼠; 1:100
赛默飞世尔 CACNA1S抗体(Pierce, MA3-920)被用于被用于免疫组化在小鼠样本上浓度为1:100. Dev Biol (2014) ncbi
小鼠 单克隆(1A)
  • 免疫组化; 小鼠
赛默飞世尔 CACNA1S抗体(Thermo scientific, MA3-920)被用于被用于免疫组化在小鼠样本上. PLoS Genet (2013) ncbi
小鼠 单克隆(1A)
  • 免疫印迹; 人类
赛默飞世尔 CACNA1S抗体(Pierce, 1A)被用于被用于免疫印迹在人类样本上. J Card Fail (2012) ncbi
艾博抗(上海)贸易有限公司
小鼠 单克隆(1A)
  • 免疫印迹; 兔; 图 1a
艾博抗(上海)贸易有限公司 CACNA1S抗体(Abcam, ab2862)被用于被用于免疫印迹在兔样本上 (图 1a). Sci Rep (2015) ncbi
西格玛奥德里奇
小鼠 单克隆(1A)
  • 免疫印迹; 小鼠
西格玛奥德里奇 CACNA1S抗体(Sigma Aldrich, D218)被用于被用于免疫印迹在小鼠样本上. FEBS Lett (2015) ncbi
默克密理博中国
小鼠 单克隆(mAB 1a)
  • 免疫组化; 小鼠; 图 4a
默克密理博中国 CACNA1S抗体(Millipore, MAB 427)被用于被用于免疫组化在小鼠样本上 (图 4a). J Cell Biol (2015) ncbi
小鼠 单克隆(mAB 1a)
  • 免疫组化-冰冻切片; 小鼠; 1:500
  • 免疫印迹; 小鼠
默克密理博中国 CACNA1S抗体(Millipore, MAB427)被用于被用于免疫组化-冰冻切片在小鼠样本上浓度为1:500 和 被用于免疫印迹在小鼠样本上. Invest Ophthalmol Vis Sci (2014) ncbi
小鼠 单克隆(mAB 1a)
  • 免疫组化-冰冻切片; 小鼠; 图 3
默克密理博中国 CACNA1S抗体(Chemicon, MAB427)被用于被用于免疫组化-冰冻切片在小鼠样本上 (图 3). PLoS ONE (2011) ncbi
文章列表
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  2. Amici D, Pinal Fernández I, Mázala D, Lloyd T, Corse A, Christopher Stine L, et al. Calcium dysregulation, functional calpainopathy, and endoplasmic reticulum stress in sporadic inclusion body myositis. Acta Neuropathol Commun. 2017;5:24 pubmed 出版商
  3. Fajardo V, Gamu D, Mitchell A, Bloemberg D, Bombardier E, Chambers P, et al. Sarcolipin deletion exacerbates soleus muscle atrophy and weakness in phospholamban overexpressing mice. PLoS ONE. 2017;12:e0173708 pubmed 出版商
  4. Linsley J, Hsu I, Groom L, Yarotskyy V, Lavorato M, Horstick E, et al. Congenital myopathy results from misregulation of a muscle Ca2+ channel by mutant Stac3. Proc Natl Acad Sci U S A. 2017;114:E228-E236 pubmed 出版商
  5. Kanzaki K, Watanabe D, Kuratani M, Yamada T, Matsunaga S, Wada M. Role of calpain in eccentric contraction-induced proteolysis of Ca2+-regulatory proteins and force depression in rat fast-twitch skeletal muscle. J Appl Physiol (1985). 2017;122:396-405 pubmed 出版商
  6. Vanhoutte D, Schips T, Kwong J, Davis J, Tjondrokoesoemo A, Brody M, et al. Thrombospondin expression in myofibers stabilizes muscle membranes. elife. 2016;5: pubmed 出版商
  7. Cong X, Doering J, Mázala D, Chin E, Grange R, Jiang H. The SH3 and cysteine-rich domain 3 (Stac3) gene is important to growth, fiber composition, and calcium release from the sarcoplasmic reticulum in postnatal skeletal muscle. Skelet Muscle. 2016;6:17 pubmed 出版商
  8. Tjondrokoesoemo A, Schips T, Kanisicak O, Sargent M, Molkentin J. Genetic overexpression of Serpina3n attenuates muscular dystrophy in mice. Hum Mol Genet. 2016;25:1192-202 pubmed 出版商
  9. Lo H, Nixon S, Hall T, Cowling B, Ferguson C, Morgan G, et al. The caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscle. J Cell Biol. 2015;210:833-49 pubmed 出版商
  10. Van B, Nishi M, Komazaki S, Ichimura A, Kakizawa S, Nakanaga K, et al. Mitsugumin 56 (hedgehog acyltransferase-like) is a sarcoplasmic reticulum-resident protein essential for postnatal muscle maturation. FEBS Lett. 2015;589:1095-104 pubmed 出版商
  11. Hu H, Wang Z, Wei R, Fan G, Wang Q, Zhang K, et al. The molecular architecture of dihydropyrindine receptor/L-type Ca2+ channel complex. Sci Rep. 2015;5:8370 pubmed 出版商
  12. Tummala S, Neinstein A, Fina M, Dhingra A, Vardi N. Localization of Cacna1s to ON bipolar dendritic tips requires mGluR6-related cascade elements. Invest Ophthalmol Vis Sci. 2014;55:1483-92 pubmed 出版商
  13. Posey A, Swanson K, Alvarez M, Krishnan S, Earley J, Band H, et al. EHD1 mediates vesicle trafficking required for normal muscle growth and transverse tubule development. Dev Biol. 2014;387:179-90 pubmed 出版商
  14. Caruso N, Herberth B, Bartoli M, Puppo F, Dumonceaux J, Zimmermann A, et al. Deregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophy. PLoS Genet. 2013;9:e1003550 pubmed 出版商
  15. Middlekauff H, Vigna C, Verity M, Fonarow G, Horwich T, Hamilton M, et al. Abnormalities of calcium handling proteins in skeletal muscle mirror those of the heart in humans with heart failure: a shared mechanism?. J Card Fail. 2012;18:724-33 pubmed 出版商
  16. Rederstorff M, Castets P, Arbogast S, Laine J, Vassilopoulos S, Beuvin M, et al. Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy. PLoS ONE. 2011;6:e23094 pubmed 出版商