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  • (1) Upstream of the T7 promoter, from -18 to -21, there is a high AT-rich region. This enhances the binding affinity of the T7 polymerase for the DNA (2) Upstream of the T7 promoter, from -22 to -27, there is a highly GC-rich region. This enhances the binding affinity of the T7 polymerase for the DNA
    4 KB (527 words) - 14:47, 11 October 2023
  • (1) Upstream of T7 promoter from -18 to -21 : With highly AT rich. It can increase binding affinity of the T7 polymerase for the DNA template (2) Upstream of T7 promoter from -22 to -27 : With highly GC rich. It can increase binding affinity of the T7 polymerase for the DNA template
    1 KB (185 words) - 05:52, 24 September 2023
  • ...ns of AR-301 (tosatoxumab) monoclonal IgG1 antibody separated by a Gly-Ser-rich linker. This part is commonly referred to as construct G (MUC-AB-G) in the * GS18 ([[Part:BBa_K4574021]]): GS-rich linker for joining variable fragments in a single-chain variable fragment (
    3 KB (463 words) - 16:29, 6 October 2023
  • ...ns of AR-301 (tosatoxumab) monoclonal IgG1 antibody separated by a Gly-Ser-rich linker. This part is commonly referred to as construct H (MUC-AB-H) in the * GS18 ([[Part:BBa_K4574021]]): GS-rich linker for joining variable fragments in a single-chain variable fragment (
    4 KB (493 words) - 16:44, 6 October 2023
  • (1) Upstream of the T7 promoter, from -18 to -21, there is a high AT-rich region. This enhances the binding affinity of the T7 polymerase for the DNA (2) Upstream of the T7 promoter, from -22 to -27, there is a highly GC-rich region. This enhances the binding affinity of the T7 polymerase for the DNA
    6 KB (812 words) - 00:00, 12 October 2023
  • (1) Upstream of the T7 promoter, from -18 to -21, there is a high AT-rich region. This enhances the binding affinity of the T7 polymerase for the DNA (2) Upstream of the T7 promoter, from -22 to -27, there is a highly GC-rich region. This enhances the binding affinity of the T7 polymerase for the DNA
    3 KB (410 words) - 21:35, 11 October 2023
  • (1) Upstream of the T7 promoter, from -18 to -21, there is a high AT-rich region. This enhances the binding affinity of the T7 polymerase for the DNA (2) Upstream of the T7 promoter, from -22 to -27, there is a highly GC-rich region. This enhances the binding affinity of the T7 polymerase for the DNA
    5 KB (742 words) - 00:01, 12 October 2023
  • (1) Upstream of the T7 promoter, from -18 to -21, there is a high AT-rich region. This enhances the binding affinity of the T7 polymerase for the DNA (2) Upstream of the T7 promoter, from -22 to -27, there is a highly GC-rich region. This enhances the binding affinity of the T7 polymerase for the DNA
    3 KB (410 words) - 21:55, 11 October 2023
  • ...f AHL is added). This effect is not seen when the cells are grown up in EZ rich media or when the cells are made to grow slower. For example, there is a dr # Cultures were diluted 1:1000 and grown for 2 hours in 4ml EZ Rich medium + Kan
    2 KB (292 words) - 21:26, 6 September 2007
  • ...pA (Scholtz 1988). A G+C rich region with dyad-symmetry followed by an A+T rich region is located at the end of the operon (E/F/repA/repC) which may be a r
    2 KB (302 words) - 05:08, 30 August 2008
  • ...e analysis of all of these promoter sequences have revealed a conserved GC rich region between the Pribnow box and the transcription start site, referred t 3. Pemberton, I.K., et al., The G+C-rich discriminator region of the tyrT promoter antagonises the formation of stab
    5 KB (786 words) - 21:10, 1 October 2011
  • ...ultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber a
    4 KB (657 words) - 14:23, 26 October 2011
  • ...ultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber a
    4 KB (662 words) - 19:47, 19 October 2011
  • ...ultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber a
    5 KB (790 words) - 14:29, 26 October 2011
  • ...ultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber a
    5 KB (842 words) - 17:21, 22 September 2011
  • ...ultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber a
    5 KB (799 words) - 17:23, 22 September 2011
  • mCherry protein with a his tag for purification and a proline rich peptide for association with SH3 domain. After Pro-rich mCherry expression, significant color change can be observed (bacteria cell
    711 B (98 words) - 16:16, 5 October 2011
  • ...ultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber a
    4 KB (662 words) - 19:49, 19 October 2011
  • ...ultured in rich medium without IPTG whilst the other group was cultured in rich medium with IPTG (4mM in 10mL). A culture of the strain holding GFP amber a
    4 KB (662 words) - 19:50, 19 October 2011
  • ...activity of the promoter may be repressed by chloramphenicol and nutrient-rich growth environment. [2] ...t al. Engineered l-Lactate Responding Promoter System Operating in Glucose-Rich and Anoxic Environments. ACS Synth Biol [Internet]. 2021;10(12):3527–36.
    5 KB (683 words) - 07:54, 9 October 2022

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