2',3'-Dideoxyguanosine-5'-Triphosphate (ddGTP) is a sugar modified nucleoside triphosphate, where the 2' and 3' hydroxyl groups are absent, resulting in chain termination. The inability of polymerases to extend from a dideoxy nucleotide causes the chain termination and is useful in a variety of biotechnology applications. ddGTP is used in cycle sequencing, enzyme mechanistic studies and for producing RNA and DNA sequences that cannot be extended by polymerases or joined by DNA ligases. Another notable application that utilizes a primer terminated on the 3′ end with a dideoxy modification is pyrophosphorolysis-activated polymerization (PAP). This technique is valuable for the detection of rare mutations. "I use ddNTPs from GlpBio for sequencing using DNA and RNA as templates and it always gives me good results." Michal Legiewicz Research Scientist Yale University
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Product Documents
Purity:>95.00%Appearance:A solid
Chemical Properties
Purity
>95.00%
Extinction Coefficient
13,600 Lmol-1cm-1 at 252 nm
Formula
C10H16N5O12P3 (free acid)
M.Wt
491.10 g/mole (free acid)
Salt Form
Li+
Concentration
100 mM
Buffer
H2O
Storage
-20°C or below
Synonyms
ddGTP
Backbone
5'-Triphosphate
Base Analog
Guanosine
Nucleotide Category
Sugar Modified
Applications
Aptamers
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