| Bioactivity | Deoxypseudouridine is a nucleoside analog. | ||||||||||||
| Invitro | Deoxypseudouridine is a nucleoside analog. Ethidium bromide staining of the gel demonstrates that the digestion of carrier DNA in both control and analog DNA samples (including Deoxypseudouridine) occur to the same extent; this indicates that the restriction enzyme is as active in the presence of the modified DNA substrate (including Deoxypseudouridine) as it is in the presence of unmodified (control) DNA. Enzymes that do not contain an AT base pair in their recognition sequence, restrict DNAs substituted with either deoxypseudouridine or deoxytubercidin as efficiently as control[1]. | ||||||||||||
| Name | Deoxypseudouridine | ||||||||||||
| CAS | 39967-60-7 | ||||||||||||
| Formula | C9H12N2O5 | ||||||||||||
| Molar Mass | 228.20 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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| Reference | [1]. Bodnar JW, et al. Effect of nucleotide analogs on the cleavage of DNA by the restriction enzymes AluI, DdeI, HinfI, RsaI, and TaqI. J Biol Chem. 1983 Dec 25;258(24):15206-13. |