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- ...2018 Hawaii iGEM team evaluated the 40 most frequently used BioBricks and ran them through an internal priming screening process that we developed using [1] Wan, X., Volpetti, F., Petrova, E., French, C., Maerkl, S. J., & Wang, B. (2019). Cascaded amplifying circuits enable ultrasensitive cellular sen16 KB (2,547 words) - 06:33, 19 October 2021
- ...2018 Hawaii iGEM team evaluated the 40 most frequently used BioBricks and ran them through an internal priming screening process that we developed using [3] Hicks M, Bachmann T T, Wang B. Synthetic biology enables programmable cell‐based biosensors[J]. ChemP24 KB (3,940 words) - 06:32, 8 October 2023
- ...control group, which was entirely in the dark state, the expression of GFP ran up to a high degree of 50,000. <br/> 2. Wang, X., Chen, X. & Yang, Y.(2012) Spatiotemporal control of gene expression7 KB (967 words) - 07:56, 18 October 2012
- ...ost characterization data on hbiF. When swapping out the fimA promoter, we ran in to two problems. The first was that part of the fimA promoter overlapped 5. Wang Q, Calvo JM. Lrp, a major regulatory protein in Escherichia coli, bends DNA4 KB (591 words) - 15:35, 29 September 2013
- ...ost characterization data on hbiF. When swapping out the fimA promoter, we ran in to two problems. The first was that part of the fimA promoter overlapped 5. Wang Q, Calvo JM. Lrp, a major regulatory protein in Escherichia coli, bends DNA4 KB (591 words) - 15:37, 29 September 2013
- ...ost characterization data on hbiF. When swapping out the fimA promoter, we ran in to two problems. The first was that part of the fimA promoter overlapped 5. Wang Q, Calvo JM. Lrp, a major regulatory protein in Escherichia coli, bends DNA4 KB (590 words) - 15:38, 29 September 2013
- ...ost characterization data on hbiF. When swapping out the fimA promoter, we ran in to two problems. The first was that part of the fimA promoter overlapped 5. Wang Q, Calvo JM. Lrp, a major regulatory protein in Escherichia coli, bends DNA4 KB (590 words) - 16:17, 29 September 2013
- ...ost characterization data on hbiF. When swapping out the fimA promoter, we ran in to two problems. The first was that part of the fimA promoter overlapped 5. Wang Q, Calvo JM. Lrp, a major regulatory protein in Escherichia coli, bends DNA4 KB (590 words) - 16:17, 29 September 2013
- <li>Cong L, Ran F A, Cox D, et al. Multiplex genome engineering using CRISPR/Cas systems[J] <li>Wang, H., Yang, H., Shivalila, C. S., Dawlaty, M. M., Cheng, A. W., Zhang, F., &43 KB (6,626 words) - 15:52, 16 July 2020
- Majumdar AS, Hughes DE, Lichtsteiner SP, Wang Z, Lebkowski JS, Vasserot AP. Ran FA, Cong L, Yan WX, Scott DA, Gootenberg JS, Kriz AJ, Zetsche B, Shalem O,7 KB (991 words) - 13:50, 17 September 2015
- ...tein by 6X /pHis-Tag behind the peptide using Nickel resin column. Then we ran the SDS-PAGE to verify the purification and analyzed the concentration of H 1. Wang, X.H.; Connor, M.; Wilson, D.C.; Wilson, H.I.; Nicholson, G.M.; Smith, R.;8 KB (1,328 words) - 13:13, 30 October 2016
- ...ith all four of our peptides, along with a randomized hybrid of 4B4/4D, we ran into difficulties in gel extracting all but 4D and P601G at a high enough c Fujishima, K., Venter, C., Wang, K., Ferreira, R., & Rothschild, L. (2015). An overhang-based DNA block shu3 KB (421 words) - 15:12, 27 October 2016
- ...ith all four of our peptides, along with a randomized hybrid of 4B4/4D, we ran into difficulties in gel extracting all but 4D and P601G at a high enough c Fujishima, K., Venter, C., Wang, K., Ferreira, R., & Rothschild, L. (2015). An overhang-based DNA block shu3 KB (429 words) - 15:17, 27 October 2016
- ...rotein by 6X His-Tag behind the peptide using Nickel resin column. Then we ran the SDS-PAGE to verify the purification and analyze the concentration of Hv 1. Wang, X.H.; Connor, M.; Wilson, D.C.; Wilson, H.I.; Nicholson, G.M.; Smith, R.;9 KB (1,474 words) - 13:43, 30 October 2016
- ...rotein by 6X His-Tag behind the peptide using Nickel resin column. Then we ran the SDS-PAGE to verify the purification and analyze the concentration of P< 4. Wang, X.H.; Connor, M.; Wilson, D.C.; Wilson, H.I.; Nicholson, G.M.; Smith, R.;10 KB (1,618 words) - 23:17, 30 October 2016
- In order to obtain more information on the localization of eCPX-nSA-cNano, we ran another SDS-PAGE gel on both the cell lysates and the resulting cellular de ....; Sell, B. R.; Allen, J. R.; Day, R. N.; Israelsson, M.; Davidson, M. W.; Wang, J. 2013. A bright monomeric green fluorescent protein derived from <i>Bran26 KB (3,937 words) - 21:45, 10 December 2016
- ...Chemie ''123'', 1116-1118.</ref> and triacetic acid lactone<ref>Frei, C., Wang, Z., Qian, S., Deutsch, S., Sutter, M., and Cirino, P. (2016). Analysis of ...raC_BBPre_F'' and ''araC_BBSuf_R'' were added and a final round of PCR was ran with the following programme: 98°C for 30s, then 30 cycles of 98°C11 KB (1,677 words) - 23:27, 31 October 2017
- ...Chemie ''123'', 1116-1118.</ref> and triacetic acid lactone<ref>Frei, C., Wang, Z., Qian, S., Deutsch, S., Sutter, M., and Cirino, P. (2016). Analysis of ...raC_BBPre_F'' and ''araC_BBSuf_R'' were added and a final round of PCR was ran with the following programme: 98°C for 30s, then 30 cycles of 98°C11 KB (1,671 words) - 23:30, 31 October 2017
- ...Chemie ''123'', 1116-1118.</ref> and triacetic acid lactone<ref>Frei, C., Wang, Z., Qian, S., Deutsch, S., Sutter, M., and Cirino, P. (2016). Analysis of ...raC_BBPre_F'' and ''araC_BBSuf_R'' were added and a final round of PCR was ran with the following programme: 98°C for 30s, then 30 cycles of 98°C11 KB (1,658 words) - 23:30, 31 October 2017
- ...Chemie ''123'', 1116-1118.</ref> and triacetic acid lactone<ref>Frei, C., Wang, Z., Qian, S., Deutsch, S., Sutter, M., and Cirino, P. (2016). Analysis of ...raC_BBPre_F'' and ''araC_BBSuf_R'' were added and a final round of PCR was ran with the following programme: 98°C for 30s, then 30 cycles of 98°C11 KB (1,656 words) - 23:08, 1 November 2017