This country code will remain if no action is taken to change it.
Our website uses functional cookies that do not collect any personal information or track your browsing activity. When you select your country, you agree that we can place these functional cookies on your device.
Descending Journal Year
Ascending Journal Year
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)
Expand Full Notes »
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
Expand Products »
We offer a range of services to help you succeed using Promega technologies. From product training to set up of automated systems and development of custom applications—our scientific support goes beyond the basics.
Ask us! We are here to help you.