| Published Application/Species/Sample/Dilution | Reference |
|---|
- immunocytochemistry; mouse; 1:100; fig 2
| Jackson S, Olufs Z, Tran K, Zaidan N, Sridharan R. Alternative Routes to Induced Pluripotent Stem Cells Revealed by Reprogramming of the Neural Lineage. Stem Cell Reports. 2016;6:302-11 pubmed publisher |
- immunohistochemistry; mouse
| Zylicz J, Dietmann S, Günesdogan U, Hackett J, Cougot D, Lee C, et al. Chromatin dynamics and the role of G9a in gene regulation and enhancer silencing during early mouse development. elife. 2015;4: pubmed publisher |
- immunocytochemistry; mouse; 1:50; fig 7
| Laurent A, Calabrese M, Warnatz H, Yaspo M, Tkachuk V, Torres M, et al. ChIP-Seq and RNA-Seq analyses identify components of the Wnt and Fgf signaling pathways as Prep1 target genes in mouse embryonic stem cells. PLoS ONE. 2015;10:e0122518 pubmed publisher |
- immunocytochemistry; mouse; 1:100
| Liskovykh M, Ponomartsev S, Popova E, Bader M, Kouprina N, Larionov V, et al. Stable maintenance of de novo assembled human artificial chromosomes in embryonic stem cells and their differentiated progeny in mice. Cell Cycle. 2015;14:1268-73 pubmed publisher |
- immunocytochemistry; mouse; 1:100; loading ...; fig 2
| Tran K, Jackson S, Olufs Z, Zaidan N, Leng N, Kendziorski C, et al. Collaborative rewiring of the pluripotency network by chromatin and signalling modulating pathways. Nat Commun. 2015;6:6188 pubmed publisher |
- immunocytochemistry; mouse; 1:200
| Zhang B, Denomme M, White C, Leung K, Lee M, Greene N, et al. Both the folate cycle and betaine-homocysteine methyltransferase contribute methyl groups for DNA methylation in mouse blastocysts. FASEB J. 2015;29:1069-79 pubmed publisher |
| Morgani S, Metzger J, Nichols J, Siggia E, Hadjantonakis A. Micropattern differentiation of mouse pluripotent stem cells recapitulates embryo regionalized cell fate patterning. elife. 2018;7: pubmed publisher |
| Joo J, Choi H, Kim M, Zaehres H, Tapia N, Stehling M, et al. Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions. Sci Rep. 2014;4:7477 pubmed publisher |
| Ohnishi Y, Huber W, Tsumura A, Kang M, Xenopoulos P, Kurimoto K, et al. Cell-to-cell expression variability followed by signal reinforcement progressively segregates early mouse lineages. Nat Cell Biol. 2014;16:27-37 pubmed publisher |
| Wu G, Han D, Gong Y, Sebastiano V, Gentile L, Singhal N, et al. Establishment of totipotency does not depend on Oct4A. Nat Cell Biol. 2013;15:1089-97 pubmed publisher |
| Han D, Tapia N, Arauzo Bravo M, Lim K, Kim K, Ko K, et al. Sox2 Level Is a Determinant of Cellular Reprogramming Potential. PLoS ONE. 2013;8:e67594 pubmed publisher |
| Gaspar Maia A, Qadeer Z, Hasson D, Ratnakumar K, Leu N, LeRoy G, et al. MacroH2A histone variants act as a barrier upon reprogramming towards pluripotency. Nat Commun. 2013;4:1565 pubmed publisher |
| Campbell J, Lane M, Vassiliev I, Nottle M. Epiblast cell number and primary embryonic stem cell colony generation are increased by culture of cleavage stage embryos in insulin. J Reprod Dev. 2013;59:131-8 pubmed |
| Liskovykh M, Chuykin I, Ranjan A, Safina D, Popova E, Tolkunova E, et al. Derivation, characterization, and stable transfection of induced pluripotent stem cells from Fischer344 rats. PLoS ONE. 2011;6:e27345 pubmed publisher |
| Agarwal S, Loh Y, McLoughlin E, Huang J, Park I, Miller J, et al. Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients. Nature. 2010;464:292-6 pubmed publisher |
