产品简要
公司名称 :
安迪生物R&D
产品类型 :
抗体
产品名称 :
SOX2抗体
目录 :
MAB2018
规格 :
100 ug (also 25 ug)
价格 :
453美元
克隆性 :
单克隆
宿主 :
小鼠
共轭标签 :
未共轭
克隆名称 :
245610
反应物种 :
人类, 小鼠, 大鼠
应用 :
免疫印迹, 免疫组化, 免疫细胞化学, 免疫组化-冰冻切片
更多信息或购买 :
文章摘录数: 177
出版应用/物种/样本/稀释参考文献
  • 免疫组化-冰冻切片; 小鼠; 图 e1g
da Silva F, Zhang K, Pinson A, Fatti E, Wilsch Bräuninger M, Herbst J, et al. Mitotic WNT signalling orchestrates neurogenesis in the developing neocortex. EMBO J. 2021;40:e108041 pubmed 出版商
  • 免疫组化; 小鼠; 1:50; 图 3d
Takeda H, Dondzillo A, Randall J, Gubbels S. Selective ablation of cochlear hair cells promotes engraftment of human embryonic stem cell-derived progenitors in the mouse organ of Corti. Stem Cell Res Ther. 2021;12:352 pubmed 出版商
  • 免疫印迹; 人类; 1:200
Xiong F, Wang R, Lee J, Li S, Chen S, Liao Z, et al. RNA m6A modification orchestrates a LINE-1-host interaction that facilitates retrotransposition and contributes to long gene vulnerability. Cell Res. 2021;31:861-885 pubmed 出版商
Berglar I, Hehlgans S, Wehle A, Roth C, Herold Mende C, R xf6 del F, et al. CHRDL1 Regulates Stemness in Glioma Stem-like Cells. Cells. 2022;11: pubmed 出版商
Govek K, Chen S, Sgourdou P, Yao Y, Woodhouse S, Chen T, et al. Developmental trajectories of thalamic progenitors revealed by single-cell transcriptome profiling and Shh perturbation. Cell Rep. 2022;41:111768 pubmed 出版商
Xiao Z, Shi G, Xi S, Singh A, Willette Brown J, Li X, et al. A TNFR1-UBCH10 axis drives lung squamous cell carcinoma dedifferentiation and metastasis through a cell-autonomous signaling loop. Cell Death Dis. 2022;13:885 pubmed 出版商
Chimienti R, Baccega T, Torchio S, Manenti F, Pellegrini S, Cospito A, et al. Engineering of immune checkpoints B7-H3 and CD155 enhances immune compatibility of MHC-I-/- iPSCs for β cell replacement. Cell Rep. 2022;40:111423 pubmed 出版商
Lauko A, Volovetz J, Turaga S, Bayık D, Silver D, Mitchell K, et al. SerpinB3 drives cancer stem cell survival in glioblastoma. Cell Rep. 2022;40:111348 pubmed 出版商
Okada M, Nakagawa Saito Y, Mitobe Y, Sugai A, Togashi K, Suzuki S, et al. Inhibition of the Phospholipase Cε-c-Jun N-Terminal Kinase Axis Suppresses Glioma Stem Cell Properties. Int J Mol Sci. 2022;23: pubmed 出版商
Pietrobono S, De Paolo R, Mangiameli D, Marranci A, Battisti I, Franchin C, et al. p38 MAPK-dependent phosphorylation of transcription factor SOX2 promotes an adaptive response to BRAF inhibitors in melanoma cells. J Biol Chem. 2022;298:102353 pubmed 出版商
Benedetti V, Banfi F, Zaghi M, Moll Diaz R, Massimino L, Argelich L, et al. A SOX2-engineered epigenetic silencer factor represses the glioblastoma genetic program and restrains tumor development. Sci Adv. 2022;8:eabn3986 pubmed 出版商
Nakagawa Saito Y, Saitoh S, Mitobe Y, Sugai A, Togashi K, Suzuki S, et al. HDAC Class I Inhibitor Domatinostat Preferentially Targets Glioma Stem Cells over Their Differentiated Progeny. Int J Mol Sci. 2022;23: pubmed 出版商
Lotila J, Hyv xe4 rinen T, Skottman H, Airas L, Narkilahti S, Hagman S. Establishment of a human induced pluripotent stem cell line (TAUi008-A) derived from a multiple sclerosis patient. Stem Cell Res. 2022;63:102865 pubmed 出版商
Khadim R, Vadivelu R, Utami T, Torizal F, Nishikawa M, Sakai Y. Integrating Oxygen and 3D Cell Culture System: A Simple Tool to Elucidate the Cell Fate Decision of hiPSCs. Int J Mol Sci. 2022;23: pubmed 出版商
Han I, Bohrer L, Gibson Corley K, Wiley L, Shrestha A, Harman B, et al. Biocompatibility of Human Induced Pluripotent Stem Cell-Derived Retinal Progenitor Cell Grafts in Immunocompromised Rats. Cell Transplant. 2022;31:9636897221104451 pubmed 出版商
Tisch M, Carmen De Mingo Alemany M, Suarez Cubero M, Fauth C, Defrancesco M, Zschocke J, et al. Generation of the human induced pluripotent stem cell line (IBKMOLi002-A) from PBMCs of a patient carrying the heterozygous L271H mutation of the voltage-gated calcium channel subunit Cav1.3-encoding CACNA1D gene. Stem Cell Res. 2022;61:102784 pubmed 出版商
Maranga C, Pereira C, Raposo A, Vieira A, Duarte S, Bekman E, et al. Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13. Stem Cell Res. 2022;61:102757 pubmed 出版商
Breyer M, Klein T, Klug K, Klopocki E, Uceyler N. Generation of the induced pluripotent stem cell line UKWNLi005-A derived from a patient with the GLA mutation c.376A > G of unknown pathogenicity in Fabry disease. Stem Cell Res. 2022;61:102747 pubmed 出版商
Polat B, Wohlleben G, Kosmala R, Lisowski D, Mantel F, Lewitzki V, et al. Differences in stem cell marker and osteopontin expression in primary and recurrent glioblastoma. Cancer Cell Int. 2022;22:87 pubmed 出版商
Zyner K, Simeone A, Flynn S, Doyle C, Marsico G, Adhikari S, et al. G-quadruplex DNA structures in human stem cells and differentiation. Nat Commun. 2022;13:142 pubmed 出版商
Notaras M, Lodhi A, Dündar F, Collier P, Sayles N, Tilgner H, et al. Schizophrenia is defined by cell-specific neuropathology and multiple neurodevelopmental mechanisms in patient-derived cerebral organoids. Mol Psychiatry. 2022;27:1416-1434 pubmed 出版商
Del Giovane A, Russo M, Tirou L, Faure H, Ruat M, Balestri S, et al. Smoothened/AMP-Activated Protein Kinase Signaling in Oligodendroglial Cell Maturation. Front Cell Neurosci. 2021;15:801704 pubmed 出版商
Pecori F, Kondo N, Ogura C, Miura T, Kume M, Minamijima Y, et al. Site-specific O-GlcNAcylation of Psme3 maintains mouse stem cell pluripotency by impairing P-body homeostasis. Cell Rep. 2021;36:109361 pubmed 出版商
Brooks B, Pradhan M, Cheng Y, Gorshkov K, Farkhondeh A, Chen C, et al. Generation of an induced pluripotent stem cell line (TRNDi031-A) from a patient with Alagille syndrome type 1 carrying a heterozygous p. C312X (c. 936 T > A) mutation in JAGGED-1. Stem Cell Res. 2021;54:102447 pubmed 出版商
Ma L, Schmidt M, Morrow E. Human iPSC lines from a Christianson syndrome patient with NHE6 W523X mutation, a biologically-related control, and CRISPR/Cas9 gene-corrected isogenic controls. Stem Cell Res. 2021;54:102435 pubmed 出版商
Notaras M, Lodhi A, Barrio Alonso E, Foord C, Rodrick T, Jones D, et al. Neurodevelopmental signatures of narcotic and neuropsychiatric risk factors in 3D human-derived forebrain organoids. Mol Psychiatry. 2021;: pubmed 出版商
Huang X, Roeder A, Li R, Beers J, Liu C, Zou J, et al. Generation of an induced pluripotent stem cell line (TRNDi012-B) from Fibrodysplasia Ossificans Progressiva (FOP) patient carrying a heterozygous mutation c. 617G > A in the ACVR1 gene. Stem Cell Res. 2021;54:102424 pubmed 出版商
Lee M, Stebbins M, Jiao H, Huang H, Leiferman E, Walczak B, et al. Comparative evaluation of isogenic mesodermal and ectomesodermal chondrocytes from human iPSCs for cartilage regeneration. Sci Adv. 2021;7: pubmed 出版商
Brooks B, Yeh C, Beers J, Liu C, Cheng Y, Gorshkov K, et al. Generation of an induced pluripotent stem cell line (TRNDi030-A) from a patient with Farber disease carrying a homozygous p. Y36C (c. 107 A>G) mutation in ASAH1. Stem Cell Res. 2021;53:102387 pubmed 出版商
Zhu W, Cheng Y, Xu M, Farkhondeh A, Beers J, Zou J, et al. Generation of Alagille syndrome derived induced pluripotent stem cell line carrying heterozygous mutation in the JAGGED-1 gene at splicing site (Chr20: 10,629,709C>A) before exon 11. Stem Cell Res. 2021;53:102366 pubmed 出版商
Silva T, Pereira C, Raposo A, Oliveira A, Arez M, Cabral J, et al. Generation and characterization of induced pluripotent stem cells heterozygous for the Portuguese BRCA2 founder mutation. Stem Cell Res. 2021;53:102364 pubmed 出版商
Lin Y, Kumar M, Ramesh N, Anderson E, Nguyen A, Kim B, et al. Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathway. Nat Neurosci. 2021;24:1077-1088 pubmed 出版商
Pradhan M, Farkhondeh A, Cheng Y, Xu M, Beers J, Zou J, et al. An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, p.R390P and p.L318P, in the NGLY1 gene. Stem Cell Res. 2021;54:102400 pubmed 出版商
Khuu M, Nallamothu T, Castro Rivera C, Arias Cavieres A, Szujewski C, Garcia Iii A. Stage-dependent effects of intermittent hypoxia influence the outcome of hippocampal adult neurogenesis. Sci Rep. 2021;11:6005 pubmed 出版商
Silva T, Pereira C, Oliveira A, Raposo A, Arez M, Cabral J, et al. Generation and characterization of induced pluripotent stem cells from a family carrying the BRCA1 mutation c.3612delA. Stem Cell Res. 2021;52:102242 pubmed 出版商
Bressan R, Southgate B, Ferguson K, Blin C, Grant V, Alfazema N, et al. Regional identity of human neural stem cells determines oncogenic responses to histone H3.3 mutants. Cell Stem Cell. 2021;28:877-893.e9 pubmed 出版商
Pasquale V, Ducci G, Campioni G, Ventrici A, Assalini C, Busti S, et al. Profiling and Targeting of Energy and Redox Metabolism in Grade 2 Bladder Cancer Cells with Different Invasiveness Properties. Cells. 2020;9: pubmed 出版商
Ji X, Tang Q, Tang C, Wu Z, Ma L, Guo X, et al. Generation of an induced pluripotent stem cell line from an Alström Syndrome patient with ALMS1 mutation (c.3902C > A, c.6436C > T) and a gene correction isogenic iPSC line. Stem Cell Res. 2020;49:102089 pubmed 出版商
Pietrobono S, Anichini G, Sala C, Manetti F, Almada L, Pepe S, et al. ST3GAL1 is a target of the SOX2-GLI1 transcriptional complex and promotes melanoma metastasis through AXL. Nat Commun. 2020;11:5865 pubmed 出版商
Xu X, Pradhan M, Xu M, Cheng Y, Beers J, Linask K, et al. Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D, TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy individuals. Stem Cell Res. 2020;49:102011 pubmed 出版商
Pecori F, Akimoto Y, Hanamatsu H, Furukawa J, Shinohara Y, Ikehara Y, et al. Mucin-type O-glycosylation controls pluripotency in mouse embryonic stem cells via Wnt receptor endocytosis. J Cell Sci. 2020;133: pubmed 出版商
Sripathy S, Wang Y, Moses R, Fatemi A, Batista D, Maher B. Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome. Stem Cell Res. 2020;48:102001 pubmed 出版商
Zalenski A, Majumder S, De K, Venere M. An interphase pool of KIF11 localizes at the basal bodies of primary cilia and a reduction in KIF11 expression alters cilia dynamics. Sci Rep. 2020;10:13946 pubmed 出版商
Muzio L, Sirtori R, Gornati D, Eleuteri S, Fossaghi A, Brancaccio D, et al. Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral Sclerosis. Nat Commun. 2020;11:3848 pubmed 出版商
Chen S, Lai W, Zhang W, Chen Q, Zhou L, So K, et al. Insulin-like growth factor 1 partially rescues early developmental defects caused by SHANK2 knockdown in human neurons. Neural Regen Res. 2020;15:2335-2343 pubmed 出版商
Kaufman G, Kiburi N, Skrtic D. The self-renewal dental pulp stem cell microtissues challenged by a toxic dental monomer. Biosci Rep. 2020;40: pubmed 出版商
Gomes I, de Almeida B, Dâmaso S, Mansinho A, Correia I, Henriques S, et al. Expression of receptor activator of NFkB (RANK) drives stemness and resistance to therapy in ER+HER2- breast cancer. Oncotarget. 2020;11:1714-1728 pubmed 出版商
Mehdipour M, Skinner C, Wong N, Lieb M, Liu C, Etienne J, et al. Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin. Aging (Albany NY). 2020;12:8790-8819 pubmed 出版商
Micali N, Kim S, Diaz Bustamante M, Stein O Brien G, Seo S, Shin J, et al. Variation of Human Neural Stem Cells Generating Organizer States In Vitro before Committing to Cortical Excitatory or Inhibitory Neuronal Fates. Cell Rep. 2020;31:107599 pubmed 出版商
Kitajima R, Nakai R, Imamura T, Kameda T, Kozuka D, Hirai H, et al. Modeling of early neural development in vitro by direct neurosphere formation culture of chimpanzee induced pluripotent stem cells. Stem Cell Res. 2020;44:101749 pubmed 出版商
Li R, Pradhan M, Xu M, Roeder A, Beers J, Zou J, et al. An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182T>C) mutation in the NPC1 gene. Stem Cell Res. 2020;44:101737 pubmed 出版商
Su L, Lei X, Ma H, Feng C, Jiang J, Jiao J. PRDM16 orchestrates angiogenesis via neural differentiation in the developing brain. Cell Death Differ. 2020;27:2313-2329 pubmed 出版商
Hengel H, Bosso Lefèvre C, GRADY G, Szenker Ravi E, Li H, Pierce S, et al. Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy. Nat Commun. 2020;11:595 pubmed 出版商
Mura M, Bastaroli F, Corli M, Ginevrino M, Calabrò F, Boni M, et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1. Stem Cell Res. 2020;42:101658 pubmed 出版商
Yoshida Y, Takahashi M, Yamanishi H, Nakazawa Y, Kishimoto J, Ohyama M. Changes in the Expression of Smooth Muscle Cell-Related Genes in Human Dermal Sheath Cup Cells Associated with the Treatment Outcome of Autologous Cell-Based Therapy for Male and Female Pattern Hair Loss. Int J Mol Sci. 2022;23: pubmed 出版商
Hyvärinen T, Hyysalo A, Kapucu F, Aarnos L, Vinogradov A, Eglen S, et al. Functional characterization of human pluripotent stem cell-derived cortical networks differentiated on laminin-521 substrate: comparison to rat cortical cultures. Sci Rep. 2019;9:17125 pubmed 出版商
Grall E, Gourain V, Nair A, Martin E, Birling M, Freund J, et al. Severe head dysgenesis resulting from imbalance between anterior and posterior ontogenetic programs. Cell Death Dis. 2019;10:812 pubmed 出版商
Stubb A, Guzman C, Närvä E, Aaron J, Chew T, Saari M, et al. Superresolution architecture of cornerstone focal adhesions in human pluripotent stem cells. Nat Commun. 2019;10:4756 pubmed 出版商
Peñaranda Fajardo N, Meijer C, Liang Y, Dijkstra B, Aguirre Gamboa R, den Dunnen W, et al. ER stress and UPR activation in glioblastoma: identification of a noncanonical PERK mechanism regulating GBM stem cells through SOX2 modulation. Cell Death Dis. 2019;10:690 pubmed 出版商
Yang S, Cheng Y, Li R, Pradhan M, Hong J, Beers J, et al. An induced pluripotent stem cell line (TRNDi010-C) from a patient carrying a homozygous p.R401X mutation in the NGLY1 gene. Stem Cell Res. 2019;39:101496 pubmed 出版商
Yao J, Wu X, Zhang D, Wang L, Zhang L, Reynolds E, et al. Elevated endothelial Sox2 causes lumen disruption and cerebral arteriovenous malformations. J Clin Invest. 2019;129:3121-3133 pubmed 出版商
Huang M, Tailor J, Zhen Q, Gillmor A, Miller M, Weishaupt H, et al. Engineering Genetic Predisposition in Human Neuroepithelial Stem Cells Recapitulates Medulloblastoma Tumorigenesis. Cell Stem Cell. 2019;: pubmed 出版商
Baskfield A, Li R, Beers J, Zou J, Liu C, Zheng W. An induced pluripotent stem cell line (TRNDi009-C) from a Niemann-Pick disease type A patient carrying a heterozygous p.L302P (c.905 T>C) mutation in the SMPD1 gene. Stem Cell Res. 2019;38:101461 pubmed 出版商
Zurkirchen L, Varum S, Giger S, Klug A, Häusel J, Bossart R, et al. Yin Yang 1 sustains biosynthetic demands during brain development in a stage-specific manner. Nat Commun. 2019;10:2192 pubmed 出版商
Howden S, Hosseini Far H, Motazedian A, Elefanty A, Stanley E, Lamande S, et al. The use of simultaneous reprogramming and gene correction to generate an osteogenesis imperfecta patient COL1A1 c. 3936 G>T iPSC line and an isogenic control iPSC line. Stem Cell Res. 2019;38:101453 pubmed 出版商
Hong J, Xu M, Li R, Cheng Y, Kouznetsova J, Beers J, et al. Generation of an induced pluripotent stem cell line (TRNDi008-A) from a Hunter syndrome patient carrying a hemizygous 208insC mutation in the IDS gene. Stem Cell Res. 2019;37:101451 pubmed 出版商
Calatayud C, Carola G, Fernandez Carasa I, Valtorta M, Jimenez Delgado S, Diaz M, et al. CRISPR/Cas9-mediated generation of a tyrosine hydroxylase reporter iPSC line for live imaging and isolation of dopaminergic neurons. Sci Rep. 2019;9:6811 pubmed 出版商
Cheng Y, Li R, Baskfield A, Beers J, Zou J, Liu C, et al. A human induced pluripotent stem cell line (TRNDi007-B) from an infantile onset Pompe patient carrying p.R854X mutation in the GAA gene. Stem Cell Res. 2019;37:101435 pubmed 出版商
Regier M, Tokar J, Warrick J, Pabon L, Berthier E, Beebe D, et al. User-defined morphogen patterning for directing human cell fate stratification. Sci Rep. 2019;9:6433 pubmed 出版商
Baskfield A, Li R, Beers J, Zou J, Liu C, Zheng W. Generation of an induced pluripotent stem cell line (TRNDi004-I) from a Niemann-Pick disease type B patient carrying a heterozygous mutation of p.L43_A44delLA in the SMPD1 gene. Stem Cell Res. 2019;37:101436 pubmed 出版商
Mura M, Lee Y, Pisano F, Ginevrino M, Boni M, Calabrò F, et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation. Stem Cell Res. 2019;37:101437 pubmed 出版商
Mura M, Lee Y, Pisano F, Ginevrino M, Boni M, Calabrò F, et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation. Stem Cell Res. 2019;37:101431 pubmed 出版商
Fadhlullah S, Halim N, Yeo J, Ho R, Um P, Ang B, et al. Pathogenic mutations in neurofibromin identifies a leucine-rich domain regulating glioma cell invasiveness. Oncogene. 2019;: pubmed 出版商
Huang W, Xu M, Li R, Baskfield A, Kouznetsova J, Beers J, et al. An induced pluripotent stem cell line (TRNDi006-A) from a MPS IIIB patient carrying homozygous mutation of p.Glu153Lys in the NAGLU gene. Stem Cell Res. 2019;37:101427 pubmed 出版商
Sherman Samis M, Onallah H, Holth A, Reich R, Davidson B. SOX2 and SOX9 are markers of clinically aggressive disease in metastatic high-grade serous carcinoma. Gynecol Oncol. 2019;153:651-660 pubmed 出版商
Stringer B, Day B, D Souza R, Jamieson P, Ensbey K, Bruce Z, et al. A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma. Sci Rep. 2019;9:4902 pubmed 出版商
Mura M, Pisano F, Stefanello M, Ginevrino M, Boni M, Calabrò F, et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene. Stem Cell Res. 2019;36:101416 pubmed 出版商
Ajmone Cat M, Onori A, Toselli C, Stronati E, Morlando M, Bozzoni I, et al. Increased FUS levels in astrocytes leads to astrocyte and microglia activation and neuronal death. Sci Rep. 2019;9:4572 pubmed 出版商
Baron D, Matheny T, Lin Y, Leszyk J, Kenna K, Gall K, et al. Quantitative proteomics identifies proteins that resist translational repression and become dysregulated in ALS-FUS. Hum Mol Genet. 2019;: pubmed 出版商
Kim H, Park H, Choi H, Chang Y, Park H, Shin J, et al. Modeling G2019S-LRRK2 Sporadic Parkinson's Disease in 3D Midbrain Organoids. Stem Cell Reports. 2019;: pubmed 出版商
Li R, Baskfield A, Beers J, Zou J, Liu C, Alméciga Díaz C, et al. Generation of an induced pluripotent stem cell line (TRNDi005-A) from a Mucopolysaccharidosis Type IVA (MPS IVA) patient carrying compound heterozygous p.R61W and p.WT405del mutations in the GALNS gene. Stem Cell Res. 2019;36:101408 pubmed 出版商
Klein T, Klug K, Henkel L, Kwok C, Edenhofer F, Klopocki E, et al. Generation of two induced pluripotent stem cell lines from skin fibroblasts of sisters carrying a c.1094C>A variation in the SCN10A gene potentially associated with small fiber neuropathy. Stem Cell Res. 2019;35:101396 pubmed 出版商
Melissaridou S, Wiechec E, Magan M, Jain M, Chung M, Farnebo L, et al. The effect of 2D and 3D cell cultures on treatment response, EMT profile and stem cell features in head and neck cancer. Cancer Cell Int. 2019;19:16 pubmed 出版商
Li R, Baskfield A, Lin Y, Beers J, Zou J, Liu C, et al. Generation of an induced pluripotent stem cell line (TRNDi003-A) from a Noonan syndrome with multiple lentigines (NSML) patient carrying a p.Q510P mutation in the PTPN11 gene. Stem Cell Res. 2019;34:101374 pubmed 出版商
Loo L, Simon J, Xing L, McCoy E, Niehaus J, Guo J, et al. Single-cell transcriptomic analysis of mouse neocortical development. Nat Commun. 2019;10:134 pubmed 出版商
Li R, Pradhan M, Xu M, Baskfield A, Farkhondeh A, Cheng Y, et al. Generation of an induced pluripotent stem cell line (TRNDi002-B) from a patient carrying compound heterozygous p.Q208X and p.G310G mutations in the NGLY1 gene. Stem Cell Res. 2019;34:101362 pubmed 出版商
Vallejo Díez S, Fleischer A, Martín Fernández J, Sanchez Gilabert A, Bachiller D. Generation of two induced pluripotent stem cells lines from a Mucopolysaccharydosis IIIB (MPSIIIB) patient. Stem Cell Res. 2018;33:180-184 pubmed 出版商
Cui C, Zhang Y, Wang C, Yuan F, Li H, Yao Y, et al. Dynamic ubiquitylation of Sox2 regulates proteostasis and governs neural progenitor cell differentiation. Nat Commun. 2018;9:4648 pubmed 出版商
Jeong M, O Reilly M, Kirkwood N, Al Aama J, Lako M, Kros C, et al. Generating inner ear organoids containing putative cochlear hair cells from human pluripotent stem cells. Cell Death Dis. 2018;9:922 pubmed 出版商
Klein T, Günther K, Kwok C, Edenhofer F, Uceyler N. Generation of the human induced pluripotent stem cell line (UKWNLi001-A) from skin fibroblasts of a woman with Fabry disease carrying the X-chromosomal heterozygous c.708 G > C (W236C) missense mutation in exon 5 of the alpha-galactosidase-A gene. Stem Cell Res. 2018;31:222-226 pubmed 出版商
Nakai R, Ohnuki M, Kuroki K, Ito H, Hirai H, Kitajima R, et al. Derivation of induced pluripotent stem cells in Japanese macaque (Macaca fuscata). Sci Rep. 2018;8:12187 pubmed 出版商
Vay S, Flitsch L, Rabenstein M, Rogall R, Blaschke S, Kleinhaus J, et al. The plasticity of primary microglia and their multifaceted effects on endogenous neural stem cells in vitro and in vivo. J Neuroinflammation. 2018;15:226 pubmed 出版商
Gao X, Yourick J, Sprando R. Generation of nine induced pluripotent stem cell lines as an ethnic diversity panel. Stem Cell Res. 2018;31:193-196 pubmed 出版商
Kwak S, Kim T, Kang B, Kim J, Lee J, Lee H, et al. Zinc finger proteins orchestrate active gene silencing during embryonic stem cell differentiation. Nucleic Acids Res. 2018;46:6592-6607 pubmed 出版商
Le O, Palacio L, Bernier G, Batinic Haberle I, Hickson G, Beausejour C. INK4a/ARF Expression Impairs Neurogenesis in the Brain of Irradiated Mice. Stem Cell Reports. 2018;10:1721-1733 pubmed 出版商
Pastor W, Liu W, Chen D, Ho J, Kim R, Hunt T, et al. TFAP2C regulates transcription in human naive pluripotency by opening enhancers. Nat Cell Biol. 2018;20:553-564 pubmed 出版商
Mura M, Ginevrino M, Zappatore R, Pisano F, Boni M, Castelletti S, et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1. Stem Cell Res. 2018;29:170-173 pubmed 出版商
Mura M, Lee Y, Ginevrino M, Zappatore R, Pisano F, Boni M, et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene. Stem Cell Res. 2018;29:157-161 pubmed 出版商
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图像
图像 1 :
安迪生物R&D MAB2018 图像 1
E-Cadherin and SOX2 antibody in BG01V Human Stem Cells by Immunocytochemistry (ICC).
产品信息
品牌 :
R&D Systems
master code :
MAB2018
SKU号 :
MAB2018
产品名称 :
SOX2抗体
描述 :
The Human/Mouse/Rat SOX2 Antibody from R&D Systems is a mouse monoclonal antibody to SOX2. This antibody reacts with human, mouse, rat. The Human/Mouse/Rat SOX2 Antibody has been validated for the following applications: Western Blot, Simple Western, Immunohistochemistry, Intracellular Staining by Flow Cytometry, Immunocytochemistry, CyTOF-reported.
靶标 :
SOX2
类别 :
一抗
单位尺寸 :
100 ug (also 25 ug)
缓冲液 :
Lyophilized from a 0.2 µm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
克隆性 :
单克隆
克隆 :
245610
浓度 :
LYOPH
共轭标签 :
未共轭
宿主 :
小鼠
免疫原 :
E. coli -derived recombinant human SOX2, Gly135-Met317, Accession # P48431
抗体亚型 :
IgG2a
纯度 :
Protein A or G purified from hybridoma culture supernatant
物种 :
人类, 小鼠, 大鼠
特异性 :
Detects human, mouse, and rat SOX2 in Western blots.
基因符号 :
SOX2
accessionNumbers :
P48431
应用 :
Western Blot, Simple Western, Immunohistochemistry, Intracellular Staining by Flow Cytometry, Immunocytochemistry, CyTOF-reported
美元 :
453美元
别名 :
ANOP3, MCOPS3, MGC2413, SRY (sex determining region Y)-box 2, SRY-related HMG-box gene 2, transcription factor SOX2, transcription factor SOX-2
储存 :
Use a manual defrost freezer and avoid repeated freeze-thaw cycles. 12 months from date of receipt, -20 to -70 °C as supplied. 1 month, 2 to 8 °C under sterile conditions after reconstitution. 6 months, -20 to -70 °C under sterile conditions after reconstitution.
更多信息或购买 :
公司信息
安迪生物R&D
上海市长宁区延安西路726号华敏翰尊国际大厦24A1
info@rndsystemschina.com.cn
http://www.rndsystemschina.com.cn
21 52380373
公司总部: 美国
R&D Systems develops and manufactures high-quality proteins and serves as a world leader in immunoassays. R&D Systems also produces quality antibodies, antibody arrays, stem cell and cell culture products, and cell selection and detection products, serving the life science and diagnostics industry.