diisopropylammonium tetrazolide (Chem Impex International)
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diisopropylammonium tetrazolide
Diisopropylammonium Tetrazolide, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/00951/Diisopropylammonium+tetrazolide/10__1021_slash_ja964427a-170-27-30
Average 95 stars, based on 2 article reviews
Diisopropylammonium Tetrazolide, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/00951/Diisopropylammonium+tetrazolide/10__1021_slash_ja964427a-170-27-30
Average 95 stars, based on 2 article reviews
diisopropylammonium tetrazolide - by Bioz Stars,
2026-09
95/100 stars
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DNA Synthesis:Article Title: The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass Substrates Article Snippet: New methods based on photolithography and surface fluorescence were used to determine photodeprotection rates and stepwise yields for light-directed oligonucleotide synthesis using photolabile 5′-(((R-methyl-2-nitropiperonyl)oxy)carbonyl)(MeNPOC)-2′-deoxynucleoside phosphoramidites on planar glass substrates.. Under near-UV illumination (primarily 365 nm) from a mercury light source, the rate of photoremoval of the MeNPOC protecting group was found to be independent of both the nucleotide and length of the growing oligomer (t1/2 ) 12 s at 27.5 mW/cm2).. A moderate dependence on solvent polarity was observed, with photolysis proceeding most rapidly in the presence of nonpolar solvents or in the absence of solvent (e.g., t1/2 ) 10-13 s at 27.5 mW/cm2). Pore Size:Article Title: The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass Substrates Article Snippet: New methods based on photolithography and surface fluorescence were used to determine photodeprotection rates and stepwise yields for light-directed oligonucleotide synthesis using photolabile 5′-(((R-methyl-2-nitropiperonyl)oxy)carbonyl)(MeNPOC)-2′-deoxynucleoside phosphoramidites on planar glass substrates.. Under near-UV illumination (primarily 365 nm) from a mercury light source, the rate of photoremoval of the MeNPOC protecting group was found to be independent of both the nucleotide and length of the growing oligomer (t1/2 ) 12 s at 27.5 mW/cm2).. A moderate dependence on solvent polarity was observed, with photolysis proceeding most rapidly in the presence of nonpolar solvents or in the absence of solvent (e.g., t1/2 ) 10-13 s at 27.5 mW/cm2). Chromatography:Article Title: The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass Substrates Article Snippet: New methods based on photolithography and surface fluorescence were used to determine photodeprotection rates and stepwise yields for light-directed oligonucleotide synthesis using photolabile 5′-(((R-methyl-2-nitropiperonyl)oxy)carbonyl)(MeNPOC)-2′-deoxynucleoside phosphoramidites on planar glass substrates.. Under near-UV illumination (primarily 365 nm) from a mercury light source, the rate of photoremoval of the MeNPOC protecting group was found to be independent of both the nucleotide and length of the growing oligomer (t1/2 ) 12 s at 27.5 mW/cm2).. A moderate dependence on solvent polarity was observed, with photolysis proceeding most rapidly in the presence of nonpolar solvents or in the absence of solvent (e.g., t1/2 ) 10-13 s at 27.5 mW/cm2). other:Article Title: Whole-body scanning PCR; a highly sensitive method to study the biodistribution of mRNAs, noncoding RNAs and therapeutic oligonucleotides Article Snippet: To a solution of 5.00 mmol of the N-protected 5′- o -biphenylsulphonyl-2′-deoxynucleoside 5–8 in 25 ml anhydrous dichloromethane under argon is added 1.28 g (7.50 Article Title: Whole-body scanning PCR; a highly sensitive method to study the biodistribution of mRNAs, noncoding RNAs and therapeutic oligonucleotides. Article Snippet: Synthesis of N-protected 50-o-biphenylsulphonyl-20-deoxynucleoside phosphoramidites To a solution of 5.00mmol of the N-protected 50-obiphenylsulphonyl-20-deoxynucleoside 5–8 in 25ml anhydrous dichloromethane under argon is added 1.28 g ( |