Oligonucleotide Synthesis, RNA Raw Materials & Modification

3'-O-cyanoethenyl-dTTP

Oligonucleotide Synthesis, RNA Raw Materials & Modification

产品编号CH66035CAS号2142998-82-9纯度>=98%
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产品概述

快速信息

产品系列
Oligonucleotide Synthesis, RNA Raw Materials & Modification
纯度
>=98%

3'-O-cyanoethenyl-dTTP is a 3'-O-cyanoethenyl modified dTTP reversible terminator. The 3'-hydroxyl is capped with a reversible blocking group so that polymerase extension stops after a single incorporation cycle. Key identifiers for this catalog entry are CHEMOS CH66035 and CAS 2142998-82-9.

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. This page keeps the identity boundary to the supplier catalog name, CAS number, and literature-supported reversible-terminator nucleotide context.

同义词

3'-O-cyanoethenyl-dTTP; 3'-O-(2-cyanovinyl)-thymidine-5'-triphosphate

身份与规格

Catalog No.CH66035
Product Name3'-O-cyanoethenyl-dTTP
CAS No.2142998-82-9
Product Type3'-O-cyanoethenyl reversible-terminator dTTP
Base AddedThymine
Purity>=98%

技术属性

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

应用背景

  • Reversible terminator nucleotide: used as the thymine 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.

相关技术资源

公开来源

常见问题

What is 3'-O-cyanoethenyl-dTTP?

3'-O-cyanoethenyl-dTTP is a 3'-O-cyanoethenyl modified dTTP 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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