产品简要
公司名称 :
赛默飞世尔
其他品牌 :
NeoMarkers, Lab Vision, Endogen, Pierce, BioSource International, Zymed Laboratories, Caltag, Molecular Probes, Research Genetics, Life Technologies, Applied Biosystems, GIBCO BRL, ABgene, Dynal, Affinity BioReagents, Nunc, Invitrogen, NatuTec, Oxoid, Richard-Allan Scientific, Arcturus, Perseptive Biosystems, Proxeon, eBioscience
产品类型 :
抗体
产品名称 :
SOX2多克隆抗体
目录 :
PA1-16968
规格 :
100微升
价格 :
美国450.00
克隆性 :
多克隆
宿主 :
domestic rabbit
共轭标签 :
未共轭
反应物种 :
人类, 小鼠, 大鼠, , 家羊
应用 :
免疫印迹, 免疫组化, 免疫细胞化学, 流式细胞仪, 免疫组化-石蜡切片
更多信息或购买 :
文章摘录数: 18
出版应用/物种/样本/稀释参考文献
  • 免疫细胞化学; 人类; 图 s4
Nickolls A, Lee M, Espinoza D, Szczot M, Lam R, Wang Q, et al. Transcriptional Programming of Human Mechanosensory Neuron Subtypes from Pluripotent Stem Cells. Cell Rep. 2020;30:932-946.e7 pubmed 出版商
  • 免疫细胞化学; 人类; 1:100; 图 1g
Alonso Barroso E, Brasil S, Briso Montiano Á, Navarrete R, Perez Cerda C, Ugarte M, et al. Generation and characterization of a human iPSC line from a patient with propionic acidemia due to defects in the PCCA gene. Stem Cell Res. 2017;23:173-177 pubmed 出版商
  • 免疫组化; 人类; 图 3
Castaño J, Morera C, Sesé B, Boue S, Bonet Costa C, Marti M, et al. SETD7 Regulates the Differentiation of Human Embryonic Stem Cells. PLoS ONE. 2016;11:e0149502 pubmed 出版商
Ortu xf1 o Costela M, Cerrada V, Moreno Izquierdo A, Garc xed a Consuegra I, Laberthonni xe8 re C, Delourme M, et al. Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology. Int J Mol Sci. 2022;23: pubmed 出版商
Cai M, Chai S, Xiong T, Wei J, Mao W, Zhu Y, et al. Aberrant Expression of Circulating MicroRNA Leads to the Dysregulation of Alpha-Synuclein and Other Pathogenic Genes in Parkinson's Disease. Front Cell Dev Biol. 2021;9:695007 pubmed 出版商
Shah N, Hallur P, Ganesh R, Sonpatki P, Naik D, Chandrachari K, et al. Gelatin methacrylate hydrogels culture model for glioblastoma cells enriches for mesenchymal-like state and models interactions with immune cells. Sci Rep. 2021;11:17727 pubmed 出版商
Fütterer A, Talavera Gutiérrez A, Pons T, de Celis J, Gutierrez J, Domínguez Plaza V, et al. Impaired stem cell differentiation and somatic cell reprogramming in DIDO3 mutants with altered RNA processing and increased R-loop levels. Cell Death Dis. 2021;12:637 pubmed 出版商
Raj N, McEachin Z, Harousseau W, Zhou Y, Zhang F, Merritt Garza M, et al. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis. Cell Rep. 2021;35:108991 pubmed 出版商
Kruminis Kaszkiel E, Osowski A, Bejer Olenska E, Dziekoński M, Wojtkiewicz J. Differentiation of Human Mesenchymal Stem Cells from Wharton's Jelly Towards Neural Stem Cells Using A Feasible and Repeatable Protocol. Cells. 2020;9: pubmed 出版商
Elfar M, Amleh A. miR-590-3p and Its Downstream Target Genes in HCC Cell Lines. Anal Cell Pathol (Amst). 2019;2019:3234812 pubmed 出版商
Gupta M, Polisetty R, Sharma R, Ganesh R, Gowda H, Purohit A, et al. Altered transcriptional regulatory proteins in glioblastoma and YBX1 as a potential regulator of tumor invasion. Sci Rep. 2019;9:10986 pubmed 出版商
López Márquez A, Alonso Barroso E, Cerro Tello G, Bravo Alonso I, Arribas Carreira L, Briso Montiano Á, et al. Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene. Stem Cell Res. 2019;38:101469 pubmed 出版商
Arellano Viera E, Zabaleta L, Castaño J, Azkona G, Carvajal Vergara X, Giorgetti A. Generation of two transgene-free human iPSC lines from CD133+ cord blood cells. Stem Cell Res. 2019;36:101410 pubmed 出版商
Haghighi F, Dahlmann J, Nakhaei Rad S, Lang A, Kutschka I, Zenker M, et al. bFGF-mediated pluripotency maintenance in human induced pluripotent stem cells is associated with NRAS-MAPK signaling. Cell Commun Signal. 2018;16:96 pubmed 出版商
Glen C, McDevitt T, Kemp M. Dynamic intercellular transport modulates the spatial patterning of differentiation during early neural commitment. Nat Commun. 2018;9:4111 pubmed 出版商
Richard E, Brasil S, Briso Montiano Á, Alonso Barroso E, Gallardo M, Merinero B, et al. Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type. Stem Cell Res. 2018;29:143-147 pubmed 出版商
Ortuño Costela M, Moreno Izquierdo A, Garesse R, Gallardo M. Generation of a human iPSC line, IISHDOi002-A, with a 46, XY/47, XYY mosaicism and belonging to an African mitochondrial haplogroup. Stem Cell Res. 2018;28:131-135 pubmed 出版商
Ventura Ferreira M, Bienert M, Muller K, Rath B, Goecke T, Opländer C, et al. Comprehensive characterization of chorionic villi-derived mesenchymal stromal cells from human placenta. Stem Cell Res Ther. 2018;9:28 pubmed 出版商
图像
图像 1 :
赛默飞世尔 PA1-16968 图像 1
FACS staining of NTERA-2 cells using PA1-16968 at a 1:50 dilution detected using Dylight-488 conjugated goat anti-rabbit IgG secondary antibody.
图像 2 :
赛默飞世尔 PA1-16968 图像 2
Immunohistochemical staining of uterus, endometrial glands using PA1-16968.
图像 3 :
赛默飞世尔 PA1-16968 图像 3
Western Blot detection of SOX2 in mouse brain lysate using PA1-16968 (0.5ug/ml).
产品信息
产品类型 :
抗体
产品名称 :
SOX2多克隆抗体
目录# :
PA1-16968
规格 :
100微升
价格 :
美国450.00
克隆性 :
多克隆
纯度 :
抗原亲和色谱
宿主 :
反应物种 :
Canine, Human, Mouse, Ovine, Rat
应用 :
Flow Cytometry: 1:100, Immunocytochemistry: 1:50-1:250, Immunohistochemistry (Paraffin): 1:125-1:250, Western Blot: 0.5 µg/mL
物种 :
Canine, Human, Mouse, Ovine, Rat
抗体亚型 :
IgG
储存 :
-20° C, 避免反复冷冻/解冻
描述 :
SOX2 is an intronless gene encoding a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of the SOX2 gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. The SOX2 gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). Further, SOX2 protein may act as a transcriptional activator after forming a protein complex with other proteins. Mutations in the SOX2 gene have been associated with bilateral anophthalmia, a severe form of structural eye malformation, optic nerve hypoplasia and syndromic microphthalmia.
免疫原 :
Synthetic peptide made to the N-terminal region of human SOX2 protein (within residues 1-100). [Swiss-Prot# P48431]
格式 :
液体
应用w/稀释 :
Flow Cytometry: 1:100, Immunocytochemistry: 1:50-1:250, Immunohistochemistry (Paraffin): 1:125-1:250, Western Blot: 0.5 µg/mL
别名 :
ANOP3; cb236; Delta EF2a; lcc; MCOPS3; MCOPS3 (Microphthalmia Syndromic type 3); RGD1565646; sex determining region Y-box 2; SOX 2; SOX2; Sox-2; soxp; SRY (sex determining region Y) box 2; SRY (sex determining region Y)-box 2; SRY box 2; SRY related HMG box 2; SRY-box 2; SRY-box 2; SOX2; SRY-box containing gene 2; SRY-box transcription factor 2; SRY-related HMG-box gene 2; transcription factor SOX2; transcription factor SOX-2; wu:fb83g04; wu:fc14d07; ysb; zgc:65860; zgc:77389
更多信息或购买 :
公司信息
赛默飞世尔
上海浦东新金桥路27号7号楼
analyze.cn@thermofisher.com
http://www.thermo.com.cn
1084193588
公司总部: 美国