laser scanner molecular dynamics model 300a computing densitometer (Molecular Dynamics Inc)
90
Structured Review
Molecular Dynamics Inc
laser scanner molecular dynamics model 300a computing densitometer
Laser Scanner Molecular Dynamics Model 300a Computing Densitometer, supplied by Molecular Dynamics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/laser+scanner+molecular+dynamics+model+300a+computing+densitometer/computing+densitometer+model+300a/pm09788740-55-14-16
Average 90 stars, based on 1 article reviews
Laser Scanner Molecular Dynamics Model 300a Computing Densitometer, supplied by Molecular Dynamics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/laser+scanner+molecular+dynamics+model+300a+computing+densitometer/computing+densitometer+model+300a/pm09788740-55-14-16
Average 90 stars, based on 1 article reviews
laser scanner molecular dynamics model 300a computing densitometer - by Bioz Stars,
2026-10
90/100 stars
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Autoradiography:Article Title: Induction of GLUT1 mRNA in response to azide and inhibition of protein synthesis. Article Snippet: Incubation of Clone 9 cells, a nontransformed rat liver cell line, in the presence of 5 mM azide results in an induction of GLUT1 mRNA which becomes detectable after ~3 h of continuous exposure to the agent.. In examining the role of on-going protein synthesis in this response, we found that: (i) the induction of GLUT1 mRNA by azide was not inhibited by anisomycin, (ii) exposure to anisomycin alone also resulted in increased GLUT1 mRNA content, and (iii) the increments in GLUT1 mRNA content in the presence of both azide and anisomycin were additive.. Following exposure to 30 μM anisomycin, the increase in GLUT1 mRNA content became evident at 1 h, reached a maximum level of ~7-fold at 3 h, then slowly decreased but remained elevated at ~2-fold control levels at 12 h. Transcription of the GLUT1 gene, estimated by nuclear run-on assay, was stimulated 1.4 ± 0.1 and 1.6 ± 0.2-fold in cells exposed to anisomycin for 1 and 2 h, respectively (p < 0.05 for both). Plasmid Preparation:Article Title: Induction of GLUT1 mRNA in response to azide and inhibition of protein synthesis. Article Snippet: Incubation of Clone 9 cells, a nontransformed rat liver cell line, in the presence of 5 mM azide results in an induction of GLUT1 mRNA which becomes detectable after ~3 h of continuous exposure to the agent.. In examining the role of on-going protein synthesis in this response, we found that: (i) the induction of GLUT1 mRNA by azide was not inhibited by anisomycin, (ii) exposure to anisomycin alone also resulted in increased GLUT1 mRNA content, and (iii) the increments in GLUT1 mRNA content in the presence of both azide and anisomycin were additive.. Following exposure to 30 μM anisomycin, the increase in GLUT1 mRNA content became evident at 1 h, reached a maximum level of ~7-fold at 3 h, then slowly decreased but remained elevated at ~2-fold control levels at 12 h. Transcription of the GLUT1 gene, estimated by nuclear run-on assay, was stimulated 1.4 ± 0.1 and 1.6 ± 0.2-fold in cells exposed to anisomycin for 1 and 2 h, respectively (p < 0.05 for both). |