tec 30s ic structure Search Results


tec 30s ic structure  (Thermo Fisher)
94
Thermo Fisher tec 30s ic structure
A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of <t>the</t> <t>TEC-30S</t> IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.
Tec 30s Ic Structure, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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neutec masticator  (Neu-tec Group)
96
Neu-tec Group neutec masticator
A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of <t>the</t> <t>TEC-30S</t> IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.
Neutec Masticator, supplied by Neu-tec Group, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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glow discharge bal-tec med 020 coating system  (BalTec Corporation)
90
BalTec Corporation glow discharge bal-tec med 020 coating system
A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of <t>the</t> <t>TEC-30S</t> IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.
Glow Discharge Bal Tec Med 020 Coating System, supplied by BalTec Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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spectrometer avantes avaspec-uls 2049 64 tec-evo  (Avantes Inc)
90
Avantes Inc spectrometer avantes avaspec-uls 2049 64 tec-evo
A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of <t>the</t> <t>TEC-30S</t> IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.
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gnss tec data  (UNAVCO Inc)
90
UNAVCO Inc gnss tec data
A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of <t>the</t> <t>TEC-30S</t> IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.
Gnss Tec Data, supplied by UNAVCO Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pro-tec barrier filter1 pl, pf 30s  (Danaher Inc)
90
Danaher Inc pro-tec barrier filter1 pl, pf 30s
A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of <t>the</t> <t>TEC-30S</t> IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.
Pro Tec Barrier Filter1 Pl, Pf 30s, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ab protection service plan for cellinsight cx7 lzr high content analysis platform  (Thermo Fisher)
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To protect your CellInsight CX7 LZR High Content Analysis Platform the best time to plan for service is at the time of instrument purchase A proactive upfront service plan provides • Greater discounts for bundling
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α tectorin shrna plasmid  (Santa Cruz Biotechnology)
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Gene Silencers generally consist of pools of three to five target specific 19 25 nucleotide sequences in length For independent verification of α tectorin gene silencing results individual duplex components or plasmids are also available
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tect3 shrna plasmid  (Santa Cruz Biotechnology)
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Gene Silencers generally consist of pools of three to five target specific 19 25 nucleotide sequences in length For independent verification of Tect3 gene silencing results individual duplex components or plasmids are also available upon
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ab protection service plan for orbitor rs microplate mover  (Thermo Fisher)
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Image Search Results


A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of the TEC-30S IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.

Journal: Nature Communications

Article Title: Structure of the 30S translation initiation complex coupled to paused RNA polymerase and its potential for riboregulation

doi: 10.1038/s41467-025-67330-2

Figure Lengend Snippet: A Schematic of the ompD transcript and MicC recognition site. B , C Cleavage time courses of ompD mRNA fragment and +83-cleavage intermediate species (see Fig. and Suppl. Fig. for representative raw data). Free ompD mRNA fragment (black), ompD 89 -TEC (green), ompD 89 -30S IC (grey) and ompD 89 -TEC-IC (red) were incubated with MicC/Hfq and then subjected to cleavage by the RNA degradosome. Reactions were stopped at indicated time points and analysed by denaturing PAGE. Data are mean ± SD from three independent reactions. Degradation trajectories of ompD were fitted to one phase exponential decay. Formation and decay of intermediates from ompD -cleavage at position +83 were fitted to two-exponential equation [I = exp(- kt ) – exp(- jt )] with degradation rate k and formation rate j . D Cleavage specificities for nucleolytic processing of site +83 in ompD in the different assembly states, expressed as the formation rate of the +83 intermediate over the degradation rate of the respective ompD fragment starting material. Data are mean ± SD from three independent reactions. E Conformational substates of the TEC-30S IC assembly. F Substate of the early expressome proposed to facilitate the accommodation of Hfq/MicC on the bound ompD mRNA. The colours of the segmented map in ( E ) correspond to the components shown in the schematic.

Article Snippet: For the coupled TEC-30S IC structure, 12,011 multi-frame movies were then collected on a 300 kV FEI Titan Krios equipped with a Gatan K3 detector.

Techniques: Incubation