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Lamandé, S.R., Shields, K.A., Kornberg, A.J., Shield, L.K. and Bateman, J.F.
Notes: These authors used Promega's pGEM®-11Zf(+) Vector for subcloning. (2040)
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Campbell, K.M., de Lecea, L., Severynse, D.M., Caron, M.G., McGrath, M.J., Sparber, S.B., Sun, L.Y., Burton, F.H.
Notes: A cDNA was subcloned into the pGEM®-11Zf(+) Vector and both sense and antisense RNA probes were produced for in situ hybridization. (1384)
Kawasaki, H., Springett, G.M., Mochizuki, N., Toki, S., Nakaya, M., Matsuda, M., Housman, D.E., Graybiel, A.M.
Notes: The pGEM®-11Zf(+) Vector was used for routine subcloning, and the resultant plasmids were used for in vitro transcription. (0926)
Yang, L., Zhang, H., Hu, G., Wang, H., Abate-Shen, C., Shen, M.M.
Notes: The pGEM®-11Zf(+) Vector was used for subcloning. (0140)
Kurtz, D.M., Rinaldo, P., Rhead, W.J., Tian, L., Millington, D.S., Vockley, J., Hamm, D.A., Brix, A.E., Lindsey, J.R., Pinkert, C.A., O'Brien, W.E., Wood, P.A.
Notes: An entire eukaryotic expression cassette (>7.5kb) was subcloned into the pGEM®-11Zf(+) Vector. An 821bp deletion in the gene was performed, and this construct was used to electroporate ES cells for the production of transgenic mice. The pGEM®-T Easy Vector System was used to clone RT-PCR products. (0866)
pGEM®-T Easy Vector System I
pGEM®-T Easy Vector System II
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