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Digoxigenin-11-dUTP
1 mM solution in TE Buffer
Digoxigenin-11-dUTP can be enzymatically incorporated into DNA/cDNA as substitute for its natural counterpart dTTP. The resulting digoxigenin-labeled DNA/cDNA probes are subsequently detected using digoxigenin-antibodies conjugated with horseradish peroxidase (HRP), alkaline phosphatase (AP) or a fluorescent dye. The 11-atom linker is attached to the C5 position of uridine to minimize the interference of DIG on the substrate incorporation by PCR polymerase. Typically1:2 Digoxigenin-11-dUTP/dTTP ratio for PCR and Nick Translation.
Chemical structure for Digoxigenin-11-dUTP *1 mM solution in TE Buffer*
Chemical structure for Digoxigenin-11-dUTP *1 mM solution in TE Buffer*
CatalogSize
Price
Quantity
1701225 nmoles
Price
 
Physical properties

Molecular weight1132.87
SolventWater
Storage, safety and handling

Certificate of OriginDownload PDF
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
CAS129030-36-0
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Page updated on October 9, 2025