这是一篇来自已证抗体库的有关
大鼠 Sst的综述,是根据13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Sst 抗体。
Sst 同义词: SRIF; SS-14; SS-28; Smst
GeneTex
小鼠 单克隆(SOM-018) | | GeneTex Sst抗体(GeneTex, SOM-018)被用于被用于免疫组化在小鼠样本上浓度为1:200 (图 6a). Front Neuroanat (2021) ncbi |
小鼠 单克隆(SOM-018) | | GeneTex Sst抗体(GeneTex, GTX7-1935)被用于被用于免疫组化在大鼠样本上浓度为1:1000 (图 s1). Front Neural Circuits (2016) ncbi |
小鼠 单克隆(SOM-018) | | GeneTex Sst抗体(GeneTex, GTX71935)被用于被用于免疫组化在大鼠样本上 (图 3). Rom J Morphol Embryol (2015) ncbi |
小鼠 单克隆(SOM-018) | - 免疫组化; 人类; 1:100
- 免疫组化; 小鼠; 1:100
| GeneTex Sst抗体(GeneTex, GTX71935)被用于被用于免疫组化在人类样本上浓度为1:100 和 被用于免疫组化在小鼠样本上浓度为1:100. Biochim Biophys Acta (2015) ncbi |
小鼠 单克隆(SOM-018) | | GeneTex Sst抗体(GeneTex, GTX71935)被用于被用于免疫组化-石蜡切片在大鼠样本上浓度为1:200. J Endocrinol (2011) ncbi |
小鼠 单克隆(SOM-018) | | GeneTex Sst抗体(GeneTex, GTX71935)被用于被用于免疫组化在大鼠样本上浓度为1:500. Eur J Neurosci (2011) ncbi |
圣克鲁斯生物技术
小鼠 单克隆(H-11) | | 圣克鲁斯生物技术 Sst抗体(Santa Cruz Biotechnology, SC-74556)被用于被用于免疫组化在小鼠样本上浓度为1:100 (图 5a). Mol Metab (2021) ncbi |
小鼠 单克隆(H-11) | | 圣克鲁斯生物技术 Sst抗体(Santa Cruz, sc-74556)被用于被用于免疫组化-冰冻切片在小鼠样本上浓度为1:50 (图 2). Front Neuroanat (2021) ncbi |
小鼠 单克隆(H-11) | | 圣克鲁斯生物技术 Sst抗体(santa Cruz, sc-74556)被用于被用于流式细胞仪在人类样本上浓度为1:200 (图 s20). Nat Commun (2016) ncbi |
大鼠 单克隆(YC7) | | 圣克鲁斯生物技术 Sst抗体(Santa Cruz, sc-47,706)被用于被用于免疫组化在人类样本上浓度为1:200. Cell Tissue Res (2014) ncbi |
赛默飞世尔
小鼠 单克隆(ICDCLS) | | 赛默飞世尔 Sst抗体(Thermo Fisher Scientific, 14-9751-80)被用于被用于免疫组化在小鼠样本上. Cell Rep (2020) ncbi |
艾博抗(上海)贸易有限公司
domestic rabbit 单克隆(EPR3359(2)) | - 免疫组化-石蜡切片; 人类; 1:100; 图 4g
| 艾博抗(上海)贸易有限公司 Sst抗体(Abcam, ab111912)被用于被用于免疫组化-石蜡切片在人类样本上浓度为1:100 (图 4g). iScience (2022) ncbi |
Bachem
| | Bachem Sst抗体(Peninsula Laboratories, IHC-8004)被用于被用于免疫组化在大鼠样本上浓度为1:4000. J Comp Neurol (2007) ncbi |
Chen K, Zhang J, Huang Y, Tian X, Yang Y, Dong A. Single-cell RNA-seq transcriptomic landscape of human and mouse islets and pathological alterations of diabetes. iScience. 2022;25:105366
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Kitakaze K, Oyadomari M, Zhang J, Hamada Y, Takenouchi Y, Tsuboi K,
et al. ATF4-mediated transcriptional regulation protects against β-cell loss during endoplasmic reticulum stress in a mouse model. Mol Metab. 2021;54:101338
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Liu J, Kashima T, Morikawa S, Noguchi A, Ikegaya Y, Matsumoto N. Molecular Characterization of Superficial Layers of the Presubiculum During Development. Front Neuroanat. 2021;15:662724
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Kement D, Reumann R, Schostak K, Vo xdf H, Douceau S, Dottermusch M,
et al. Neuroserpin Is Strongly Expressed in the Developing and Adult Mouse Neocortex but Its Absence Does Not Perturb Cortical Lamination and Synaptic Proteome. Front Neuroanat. 2021;15:627896
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Viloria K, Nasteska D, Briant L, Heising S, Larner D, Fine N,
et al. Vitamin-D-Binding Protein Contributes to the Maintenance of α Cell Function and Glucagon Secretion. Cell Rep. 2020;31:107761
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Zhang L, Hernandez V, Vázquez Juárez E, Chay F, Barrio R. Thirst Is Associated with Suppression of Habenula Output and Active Stress Coping: Is there a Role for a Non-canonical Vasopressin-Glutamate Pathway?. Front Neural Circuits. 2016;10:13
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Saxena P, Heng B, Bai P, Folcher M, Zulewski H, Fussenegger M. A programmable synthetic lineage-control network that differentiates human IPSCs into glucose-sensitive insulin-secreting beta-like cells. Nat Commun. 2016;7:11247
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Orbán Kis K, Szabadi T, Szilágyi T. The loss of Ivy cells and the hippocampal input modulatory O-LM cells contribute to the emergence of hyperexcitability in the hippocampus. Rom J Morphol Embryol. 2015;56:155-61
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Aragón F, Karaca M, Novials A, Maldonado R, Maechler P, Rubà B. Pancreatic polypeptide regulates glucagon release through PPYR1 receptors expressed in mouse and human alpha-cells. Biochim Biophys Acta. 2015;1850:343-51
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Jabari S, da Silveira A, de Oliveira E, Quint K, Wirries A, Neuhuber W,
et al. Mucosal layers and related nerve fibres in non-chagasic and chagasic human colon--a quantitative immunohistochemical study. Cell Tissue Res. 2014;358:75-83
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Romero Zerbo S, Rafacho A, Diaz Arteaga A, Suarez J, Quesada I, Imbernon M,
et al. A role for the putative cannabinoid receptor GPR55 in the islets of Langerhans. J Endocrinol. 2011;211:177-85
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Corteen N, Cole T, Sarna A, Sieghart W, Swinny J. Localization of GABA-A receptor alpha subunits on neurochemically distinct cell types in the rat locus coeruleus. Eur J Neurosci. 2011;34:250-62
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Muller J, Mascagni F, McDonald A. Postsynaptic targets of somatostatin-containing interneurons in the rat basolateral amygdala. J Comp Neurol. 2007;500:513-29
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