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  • 1
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed-phase separation ; Oligodeoxyribonucleotides ; Isolation of pure material
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A reversed-phase chromatographic column suitable for the purification of chemically synthesized large oligodeoxyribonucleotides (oligo-DNA) was prepared. The specifications of this column are; the selected silica (Toyo Soda silica) with large pore size (at least 150 Å) and small particle diameter (5 μm desired) should be grafted only with monochloro alkylating reagent of long alkyl chain (sufficiently C18) so that the carbon content of the resultant packing material is 15–16%. Using this column, we could isolate the targeted large oligo-DNA (up to 50mer) in a large scale (75 μg per one cycle) from the impurities in the reaction mixture formed during the automated synthesis by the phosphite method.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1612-1112
    Keywords: Size-exclusion chromatography ; Polyvinyl alcohol gel column ; Oligonucleotides ; Hydrophobic interaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Separation mechanisms for single-stranded oligodeoxyribo-or oligoribonucleic acid fragments were explored on an Asahipak polyvinyl alcohol gel column (GS-320) by use of sequential isomers of such molecules. Substrates having different base numbers were found to be separated by size-exclusion chromatography while those having the same numbers with different base sequences were isolated by use of the reversed-phase mode. By using those dual modes, a limit for the separation of the samples was found to arise because one mode shifted the peaks of the substrates in the sense opposite to the shift resulting from the other mode and it was found that when substrates had less than nine bases, the solutes eluted separately.
    Type of Medium: Electronic Resource
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