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pMB1610_pRR-Puro Citations (7)

Originally described in: Single-Step Generation of Conditional Knockout Mouse Embryonic Stem Cells.
Flemr M, Buhler M Cell Rep. 2015 Jul 28;12(4):709-16. doi: 10.1016/j.celrep.2015.06.051. Epub 2015 Jul 16.
PubMed Journal

Articles Citing pMB1610_pRR-Puro

De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Basilicata MF, Bruel AL, Semplicio G, Valsecchi CIK, Aktas T, Duffourd Y, Rumpf T, Morton J, Bache I, Szymanski WG, Gilissen C, Vanakker O, Ounap K, Mittler G, van der Burgt I, El Chehadeh S, Cho MT, Pfundt R, Tan TY, Kirchhoff M, Menten B, Vergult S, Lindstrom K, Reis A, Johnson DS, Fryer A, McKay V, Fisher RB, Thauvin-Robinet C, Francis D, Roscioli T, Pajusalu S, Radtke K, Ganesh J, Brunner HG, Wilson M, Faivre L, Kalscheuer VM, Thevenon J, Akhtar A. Nat Genet. 2018 Oct;50(10):1442-1451. doi: 10.1038/s41588-018-0220-y. Epub 2018 Sep 17. PubMed
ChromID identifies the protein interactome at chromatin marks. Villasenor R, Pfaendler R, Ambrosi C, Butz S, Giuliani S, Bryan E, Sheahan TW, Gable AL, Schmolka N, Manzo M, Wirz J, Feller C, von Mering C, Aebersold R, Voigt P, Baubec T. Nat Biotechnol. 2020 Mar 2. pii: 10.1038/s41587-020-0434-2. doi: 10.1038/s41587-020-0434-2. PubMed

Associated Plasmids

High-Resolution In Vivo Identification of miRNA Targets by Halo-Enhanced Ago2 Pull-Down. Li X, Pritykin Y, Concepcion CP, Lu Y, La Rocca G, Zhang M, King B, Cook PJ, Au YW, Popow O, Paulo JA, Otis HG, Mastroleo C, Ogrodowski P, Schreiner R, Haigis KM, Betel D, Leslie CS, Ventura A. Mol Cell. 2020 Jul 2;79(1):167-179.e11. doi: 10.1016/j.molcel.2020.05.009. Epub 2020 Jun 3. PubMed
Erratic and blood vessel-guided migration of astrocyte progenitors in the cerebral cortex. Tabata H, Sasaki M, Agetsuma M, Sano H, Hirota Y, Miyajima M, Hayashi K, Honda T, Nishikawa M, Inaguma Y, Ito H, Takebayashi H, Ema M, Ikenaka K, Nabekura J, Nagata KI, Nakajima K. Nat Commun. 2022 Nov 2;13(1):6571. doi: 10.1038/s41467-022-34184-x. PubMed
EndophilinA-dependent coupling between activity-induced calcium influx and synaptic autophagy is disrupted by a Parkinson-risk mutation. Bademosi AT, Decet M, Kuenen S, Calatayud C, Swerts J, Gallego SF, Schoovaerts N, Karamanou S, Louros N, Martin E, Sibarita JB, Vints K, Gounko NV, Meunier FA, Economou A, Versees W, Rousseau F, Schymkowitz J, Soukup SF, Verstreken P. Neuron. 2023 May 3;111(9):1402-1422.e13. doi: 10.1016/j.neuron.2023.02.001. Epub 2023 Feb 23. PubMed
Dissecting the roles of MBD2 isoforms and domains in regulating NuRD complex function during cellular differentiation. Schmolka N, Karemaker ID, Cardoso da Silva R, Recchia DC, Spegg V, Bhaskaran J, Teske M, de Wagenaar NP, Altmeyer M, Baubec T. Nat Commun. 2023 Jun 29;14(1):3848. doi: 10.1038/s41467-023-39551-w. PubMed
The SMN complex drives structural changes in human snRNAs to enable snRNP assembly. Panek J, Roithova A, Radivojevic N, Sykora M, Prusty AB, Huston N, Wan H, Pyle AM, Fischer U, Stanek D. Nat Commun. 2023 Oct 18;14(1):6580. doi: 10.1038/s41467-023-42324-0. PubMed

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