
Amino-11-dCTP
| Catalog Number | R11-0007 |
| Category | Triphosphates |
| Molecular Formula | C18H63Li3N5O32P3 |
| Molecular Weight | 975.45 |
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Product Introduction
Amino-11-dCTP has the base modification in 5-position of pyrimidine to introduce primary amine groups via enzymatic reaction. The resulting DNA molecule allows further labeling with amino-reactive reagents.
Chemical Information
Application
Chemical Information
| Appearance | Off White Solid |
Application
Amino-11-dCTP is a modified deoxycytidine triphosphate designed for incorporation into nucleic acids, enabling downstream functionalization workflows that rely on click chemistry-compatible handles. As a nucleotide analog used in bioorthogonal labeling strategies, it provides a programmable way to introduce a reactive functional group at defined positions within DNA or RNA during enzymatic synthesis. In research settings, Amino-11-dCTP is commonly selected to generate clickable nucleic acid constructs for probe development, material patterning, and molecular imaging reagent preparation.
1. DNA And RNA Labeling
Amino-11-dCTP is widely used to introduce a clickable amino-functionalized nucleotide into DNA or RNA during enzymatic synthesis, giving researchers a handle for subsequent conjugation steps. This approach is particularly valuable when spatial control over labeling is needed, such as preparing sequence-defined oligonucleotides for binding studies, hybridization-based assays, or structural investigations. The resulting functional nucleic acids serve as versatile platforms for attaching dyes, affinity tags, or other reporters through click-compatible chemistries, supporting workflows that require modular post-synthetic modification.
2. Clickable Probe Conjugation
Amino-11-dCTP is frequently employed to create nucleic acid probes that can be readily converted into fluorescent, affinity, or immobilized detection reagents using click chemistry. Laboratories developing hybridization probes, sequencing-adjacent labeling tools, and nucleic-acid-based sensors often prefer nucleotide-incorporated handles because they reduce the need for harsh post-modification conditions that can compromise probe integrity. After incorporation, the clickable functionality enables efficient coupling to imaging dyes or enrichment ligands, facilitating the generation of probe conjugates for microscopy, flow-based readouts, and instrument-compatible reagent formats.
3. Molecular Imaging Constructs
Amino-11-dCTP supports the preparation of imaging-ready nucleic acid constructs by enabling site-specific introduction of a functional group that can be carried into click-based conjugation. Molecular imaging research groups use these modified oligonucleotides to generate labeled strands for probe libraries, imaging reagent optimization, and multimodal labeling strategies where fluorophores or other reporters are appended after nucleic acid synthesis. The nucleotide-based incorporation strategy helps maintain consistent probe architecture while allowing rapid exchange of imaging moieties through standardized click conjugation chemistry.
4. Biomaterials DNA Patterning
Amino-11-dCTP is used in biomaterials and surface engineering contexts where nucleic acids act as programmable building blocks for patterned interfaces. By incorporating the clickable nucleotide into DNA strands, researchers can create addressable layers that are later coupled to complementary surfaces, linkers, or functional polymers via click chemistry. This enables fabrication of DNA-based coatings, spatially organized capture platforms, and hybrid material constructs used in materials science, diagnostics reagent development, and research tool generation where controlled presentation of nucleic acid functionality is required.
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