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C8-Alkyne-dCTP

Modified triphosphate for incorporation in PCR reaction

Size Catalog No. Price
1 µmol BCT-06-S  100,00
5 µmol BCT-06-L  300,00
Clear

Chemical Properties

  • Molecular Formula

    C17H24N3O13P3

  • Shelf Life

    12 months unopened after receipt

  • Storage Conditions

    -20 °C

  • Molecular Weight

    571.31 g/mol

  • Purity

    ≥ 95% (HPLC)

  • Physical State

    100 mM solution in water (pH 7.5); clear colorless to light yellow solution

  • CAS Number

    1374991-80-6 (sodium salt)

    1004297-66-8 (free acid)

  • Absorption (max)

    λmax = 295 nm

  • Ɛ (max)

    9,500 cm-1M-1

Product Information

High-Purity Modified dCTP for Precision DNA Labeling via Click Chemistry

C8-Alkyne-dCTP is a chemically engineered deoxycytidine triphosphate (dCTP) featuring an alkyne moiety at the C8 position of cytosine. This strategic modification enables bioorthogonal conjugation via Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC), making it a powerful tool for site-specific DNA labeling, molecular tracking, and functionalization during enzymatic synthesis. Unlike conventional labeling reagents, C8-Alkyne-dCTP integrates directly into DNA strands during synthesis, streamlining workflows and enhancing reproducibility. Its compatibility with widely used DNA polymerases and mild reaction conditions.

 

Why Buy C8-Alkyne-dCTP?

DNA modification has long faced challenges:

  • Natural nucleotides lack reactive chemical groups, limiting functionalization.
  • DNA polymerases often reject modified nucleotides or incorporate them inefficiently.
  • Earlier labeling methods were non-specific and lacked control over modification sites.
  • Traditional conjugation techniques required harsh conditions that could damage DNA or disrupt biological systems.

C8-Alkyne-dCTP overcomes these limitations with several key advantages:

  • Bioorthogonal Reactivity: The alkyne group enables highly selective reactions with azide-containing molecules via CuAAC. This reaction is efficient, specific, and occurs under mild, aqueous conditions, preserving DNA integrity.
  • Enhanced Polymerase Compatibility: Compatible with family B polymerases (Pwo, Deep Vent exo-, KOD XL) and family A polymerase Taq, ensuring smooth and efficient incorporation into DNA strands.
  • Site-Specific Functionalization: Researchers can precisely control nucleotide incorporation, enabling targeted modification of DNA sequences for high-resolution applications.
  • Physiological Reaction Conditions: Click chemistry is aqueous and biologically compatible, allowing safe and reliable DNA modification in sensitive environments.
  • Safe dNTP Quantification & Chemotherapeutic Monitoring: Replaces traditional radioisotope-based detection with fluorophore-based assays, improving safety, throughput, and reproducibility in cancer research and drug monitoring workflows.
Applications of C8-Alkyne-dCTP

Applications of C8-Alkyne-dCTP

C8-Alkyne-dCTP is a versatile reagent used across multiple research and diagnostic fields:

  • Fluorescent DNA Labeling
    Enables high-resolution microscopic imaging and real-time tracking of DNA interactions.
  • Pull-Down Assays
    Facilitates biotin-azide conjugation for identifying DNA-binding proteins and studying protein-DNA interactions.
  • DNA Origami & Nanostructure Functionalization
    Supports nanotechnology applications, including DNA metallization for nanoelectronics and biosensors.
  • Targeted Drug Delivery & Molecular Diagnostics
    Allows precise DNA modifications for therapeutic targeting, biomarker detection, and custom assay development.

 

LITERATURE

Synthesis of Highly Modified DNA by a Combination of PCR with Alkyne-Bearing Triphosphates and Click Chemistry, J. Gierlich et al., 2007, Chem. – A Eur. J., Vol. 13, p. 9486–9494.

https://doi.org/10.1002/chem.200700502

Directed DNA Metallization, G. A. Burley et al., 2006, J. Am. Chem. Soc., Vol. 128, p. 1398–1399.

https://doi.org/10.1021/ja055517v

Quantitation of deoxynucleoside triphosphates by click reactions, C. Y. Huang et al., 2020, Scientific Reports, Vol. 10(1), p. 611.

https://doi.org/10.1038/s41598-020-57463-3

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