CHEMOS
Oligonucleotide Synthesis, RNA Raw Materials & Modification

3'-O-allyl-2'-dATP

Oligonucleotide Synthesis, RNA Raw Materials & Modification

N.º de productoCH66022N.º CAS917766-44-0Pureza>=98%
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Familia de productos
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Pureza
>=98%

3'-O-allyl-2'-dATP is a 3'-O-allyl modified dATP reversible terminator. The 3'-hydroxyl is capped with a reversible blocking group so that polymerase extension stops after a single incorporation cycle. Key identifiers are CHEMOS CH66022, CAS 917766-44-0, molecular formula C13H20N5O12P3, and molecular weight 531.25.

3'-O-modified nucleotides are used in cyclic reversible-terminator sequencing-by-synthesis workflows: DNA polymerase incorporates the nucleotide, extension pauses after one base, and cap removal regenerates the 3'-OH so synthesis can continue.

Sinónimos

3'-O-allyl-dATP; 3'-O-(prop-2-en-1-yl)-2'-deoxyadenosine-5'-triphosphate

Identidad y especificaciones

Catalog No.CH66022
Product Name3'-O-allyl-2'-dATP
CAS No.917766-44-0
Molecular FormulaC13H20N5O12P3
Molecular Weight531.25
Product Type3'-O-allyl reversible-terminator dATP
Base AddedAdenine
Purity>=98%

Atributos técnicos

Nucleotide class
Reversible-terminator dNTP
Parent nucleotide
dATP
3'-O blocking group
Allyl
Deblocking outcome
Regenerates the 3'-OH
Packaging
Custom packaging on request

Contexto de aplicación

  • Reversible terminator nucleotide: used as the adenine member of a 3'-O-blocked dNTP set.
  • Sequencing-by-synthesis context: incorporation pauses extension for one cycle before cap removal allows synthesis to continue.
  • Modified nucleotide cataloging: relevant to oligonucleotide synthesis, sequencing reagent, and modified dNTP product organization.

Recursos técnicos relacionados

Fuentes públicas

Preguntas frecuentes

What is 3'-O-allyl-2'-dATP?

3'-O-allyl-2'-dATP is a 3'-O-allyl modified dATP used as a reversible-terminator nucleotide in sequencing-by-synthesis research workflows.

How does a reversible terminator work?

DNA polymerase incorporates the nucleotide, the 3'-O blocking group pauses further extension, and removal of the cap regenerates the 3'-OH so synthesis can continue.

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