Catalog No.
Product Name
Application
Product Information
Citations
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Phosphoramidite Monomer
2'-OMe-A(Bz) Phosphoramidite is a modified phosphoramidite monomer designed for oligonucleotide synthesis. This compound incorporates a 2'-O-methyl modification and a benzoyl protective group, enhancing the stability and efficiency of synthesized oligonucleotides. It is highly relevant in research applications involving gene expression studies, antisense oligonucleotide design, and RNA interference. -
Phosphoramidite Monomer
DMT-dG(ib) Phosphoramidite is a phosphoramidite monomer utilized in the synthesis of DNA and nucleic acid derivatives. It serves as a key building block for creating oligonucleotides, enabling researchers to investigate genetic sequences and design nucleic acid-based applications. This reagent is essential for studies in genomics, molecular biology, and various therapeutic research areas. -
Phosphoramidite
Bz-rA Phosphoramidite is a phosphoramidite that features a 5' DMT and adenosine (A) with benzoyl (Bz) base protection. This reagent is specifically designed for the efficient synthesis of oligonucleotides. Its reliable incorporation of benzoyl-protected adenosine monomers facilitates studies in gene expression, molecular biology, and nucleic acid research. -
Phosphoramidite Derivative
DMT-dC(ac) Phosphoramidite is a phosphoramidite derivative primarily utilized in oligonucleotide synthesis. This compound serves as a protected form of deoxycytidine and plays a critical role in facilitating the incorporation of dC residues during the assembly of nucleic acid strands. Its use in solid-phase synthesis enables researchers to create diverse oligonucleotides for applications in molecular biology and genetic research. -
Phosphoramidite Monomer
DMT-2'-F-Bz-dA is a phosphoramidite monomer utilized in the synthesis of oligonucleotides. This compound features a 2'-fluoro substitution, which enhances the stability and specificity of nucleic acid interactions. It is particularly valuable in the design of modified oligonucleotides for applications in gene editing, antisense technologies, and molecular diagnostics. -
Phosphoramidites
2-O-DMT-Sulfonyldiethanol phosphoramidite is a phosphoramidite reagent essential for oligonucleotide synthesis. Its primary mechanism involves the formation of phosphodiester linkages, facilitating the assembly of nucleic acid sequences. This compound is widely utilized in molecular biology for the development of DNA and RNA oligonucleotides for research applications, including gene expression studies and therapeutic development. -
Phosphoramidite
Dmt-2'-f-dc(ac) amidite is a phosphoramidite used in the synthesis of cyclic purine dinucleotides. This compound facilitates the incorporation of modified nucleotides in oligonucleotide synthesis, allowing for enhanced stability and altered biological activity in nucleic acid studies. Its applications extend to research in nucleic acid therapeutics, gene regulation, and other molecular biology fields. -
Phosphoramidites
DMT-2'-F-6-chloro-dA phosphoramidite is a specialized phosphoramidite used for the synthesis of oligonucleotides. Its incorporation into oligonucleotide sequences allows for the introduction of fluorinated modifications, enhancing stability and specificity. This reagent is essential for chemical biology applications and the development of nucleic acid-based therapeutics. -
Phosphoramidite Monomer
2'-O-Me-C(Bz) Phosphoramidite is a modified phosphoramidite monomer targeting oligonucleotide synthesis. This reagent is instrumental in the production of RNA oligonucleotides, offering enhanced stability and improved biochemical properties. Its applications include the development of antiviral agents and therapeutics through the manipulation of RNA structures. -
dIPhosphoramidite
DMT-dA(PAc) Phosphoramidite is a dIPhosphoramidite that serves as an essential building block for the synthesis of DNA and RNA oligonucleotides. This reagent is specifically designed to facilitate the incorporation of deoxyadenosine into nucleic acid sequences, providing researchers with the ability to produce modified oligonucleotides for various applications, including genetic engineering, antisense therapy, and molecular diagnostics. Its protective groups ensure stable synthesis while maintaining high efficiency in coupling reactions. -
Phosphoramidite Monomer
S-cEt-U phosphoramidite is a modified phosphoramidite monomer designed for use in oligonucleotide synthesis. This reagent facilitates the incorporation of modified nucleotides into DNA or RNA sequences, expanding the versatility of synthetic oligonucleotides. Its application is critical in various fields, including gene therapy, antisense oligonucleotide development, and the creation of innovative bioconjugates. -
Phosphoramidites
DMT-2'-F-dA(bz) phosphoramidite is a phosphoramidite specifically designed for the synthesis of oligonucleotides. This compound facilitates the incorporation of 2'-fluoro-deoxyadenosine residues into nucleic acid sequences, enhancing the stability and biological activity of the resulting oligonucleotides. Its applications are significant in fields such as gene therapy, antisense oligonucleotide research, and RNA interference studies. -
Phosphoramidites
DMT-2'O-Methyl-rC(tac) Phosphoramidite is a specialized phosphoramidite utilized in the synthesis of oligonucleotides. This compound facilitates the incorporation of 2'-O-methyl modified ribonucleosides, enhancing the stability and binding affinity of RNA sequences. Its applications are significant in molecular biology for constructing RNA oligonucleotides with improved properties for research and therapeutic purposes. -
Phosphoramidite Monomer
DMT-dI Phosphoramidite is a modified phosphoramidite monomer that serves as a key building block in oligonucleotide synthesis. This compound facilitates the efficient incorporation of deoxyinosine into nucleic acid strands, enhancing the diversity of synthetic oligonucleotides. Its application is essential for various research areas, including gene synthesis, RNA interference studies, and the development of diagnostic tools. -
Cytosine Phosphoramidite
Ac-rC Phosphoramidite is a cytosine phosphoramidite utilized in the chemical synthesis of RNA oligonucleotides. It facilitates the incorporation of cytidine nucleotides into synthetic RNA strands while maintaining the structural integrity of the molecule during complex synthetic procedures through its specialized protecting groups. This reagent is essential for advances in RNA-based research and applications in genetic engineering and antiviral studies. -
Phosphoramidite Monomer
Fmoc-protected DMT-Dt PEG2 NH2 amidite is a phosphoramidite monomer designed for oligonucleotide synthesis. This compound features a protective Fmoc group and a PEG2 linker, enhancing solubility and facilitating the incorporation of amine functionalities into nucleic acids. It is ideal for applications in DNA and RNA synthesis, enabling the development of complex oligonucleotide structures for research in genomics and therapeutic applications. -
Phosphoramidites
DMT-2'-OMe-dA(bz) phosphoramidite is a versatile phosphoramidite used primarily for the synthesis of oligonucleotides. This modified nucleoside contributes to enhanced stability and solubility in synthetic applications. It is suitable for various research applications, including molecular biology, gene synthesis, and diagnostic development. -
Phosphoramidites
N4-Benzoyl-5’-O-(4,4’-dimethoxytrityl)-3’-deoxy-3’-fluoro-beta-D-xylofuranosyl cytidine-2’-CED-phosphoramidite is a phosphoramidite utilized in the synthesis of oligonucleotides. Its structural properties enhance the incorporation of modified nucleotides, contributing to the development of oligonucleotides with improved stability and biological activity. This reagent is valuable for applications in gene modulation, nucleic acid research, and the exploration of antisense and RNA interference strategies. -
Phosphoramidites
DMT-2'-F-dA Phosphoramidite is a modified phosphoramidite that serves as a key reagent in the synthesis of oligonucleotides. Its unique structure incorporates a fluorine atom at the 2' position, enabling enhanced stability and functionality of nucleic acids. This compound is essential for researchers in the fields of molecular biology and genetic engineering, facilitating the development of tailored oligonucleotide sequences for various applications, including diagnostics and therapeutics. -
Phosphoramidites
DMT-LNA-5mA phosphoramidite is a versatile phosphoramidite used primarily for the synthesis of oligonucleotides. Its unique structure features an LNA (locked nucleic acid) modification, enhancing the binding affinity and specificity of oligonucleotide probes. This reagent is essential for applications in molecular biology, including gene expression analysis, antisense oligonucleotide development, and RNA interference studies. -
Phosphoramidites
DMT-LNA-G phosphoramidite is a phosphoramidite that facilitates the synthesis of locked nucleic acid (LNA) containing oligonucleotides. Its unique chemical structure enhances binding affinity and stability of nucleic acid probes, improving their performance in various applications such as molecular diagnostics, RNA interference, and antisense therapy. This reagent is essential for researchers focused on the development of innovative nucleic acid-based therapeutics and tools. -
Phosphoramidites
DMT-2'-O-TBDMS-G(dmf)-CE-phosphoramidite is a phosphoramidite utilized in the synthesis of oligonucleotides. This compound serves as a key building block, facilitating the incorporation of modified nucleotides during solid-phase synthesis. Its biological activity supports research applications in gene synthesis, antisense oligonucleotide development, and RNA interference studies. As a versatile reagent, it enables advancements in nucleic acid research and therapeutic applications. -
Phosphoramidites
DMT-2'-F-Cytidine Phosphoramidite is a specialized phosphoramidite compound used in the synthesis of oligonucleotides. This reagent facilitates the introduction of a 2'-fluorine modification, enhancing the stability and affinity of oligonucleotide therapeutics. Its application is crucial in studying nucleic acid interactions and developing novel antisense and RNAi strategies. -
Nucleoside Phosphoramidite
FAM-dT phosphoramidite is a fully protected nucleoside phosphoramidite that facilitates the incorporation of fluorescent labels into oligonucleotides. This compound enables the synthesis of labeled oligonucleotides for various applications, including DNA sequencing, molecular diagnostics, and fluorescence-based assays. Its fluorescent properties make it particularly useful for studies involving gene expression and nucleotide interactions. -
Phosphoramidite Compound
(S)-GNA-T-phosphoramidite is a phosphoramidite compound utilized in the synthesis of oligonucleotides. This reagent is essential for the construction of nucleic acid sequences in various research applications, including gene therapy, molecular diagnostics, and genetic engineering. Its reliable performance makes it an important tool in the field of synthetic biology and nucleic acid chemistry. -
Phosphoramidites
Bis(2-(trimethylsilyl)ethyl) diisopropylphosphoramidite is a phosphoramidite reagent designed for oligonucleotide synthesis. Its primary mechanism involves the introduction of phosphoramidite linkages in nucleic acid constructs. This compound is suitable for applications in molecular biology, including the development of DNA and RNA oligonucleotides for research in gene expression, antisense therapy, and RNA interference studies. -
Phosphoramidite Analogue
5'-DMT-5-F-2'-dU Phosphoramidite is a nucleoside phosphoramidite analogue designed for use in oligonucleotide synthesis. This compound facilitates the development of therapeutic oligonucleotides, with potential applications in creating drugs aimed at targeting various cancers. Its unique structure allows for incorporation into synthesized sequences, enhancing the efficacy of emerging RNA-based therapies. -
Phosphoramidite Derivative
DMT-2′Fluoro-dU Phosphoramidite is a phosphoramidite derivative of uridine with a fluorine atom at the 2' position. This reagent is designed for nucleoside modification, enabling the synthesis of modified DNA sequences. It is particularly useful in the development of oligonucleotides for applications in molecular biology and genetic research. -
Phosphoramidite Monomer
2'-OMe-G(ibu) Phosphoramidite is a modified phosphoramidite monomer designed for oligonucleotide synthesis. This compound incorporates a 2'-O-methyl group, which enhances the stability and hybridization properties of RNA oligonucleotides. It is particularly useful in studies involving RNA structure, function, and therapeutics, enabling researchers to create modified nucleic acids with improved pharmacological profiles. -
5-Fluoro-2'-deoxycytidine Phosphoramidite
DMTr-5-fluoro-2'-deoxycytidine-phosphoramidite functions as a phosphoramidite derivative of 5-fluoro-2'-deoxycytidine, specifically designed for use in solid-phase oligonucleotide synthesis. This reagent enables the incorporation of the nucleoside analogue into DNA sequences, facilitating studies of nucleotide metabolism, DNA repair mechanisms, and the effects of fluorinated nucleotides on enzyme activity. Its chemical structure allows for efficient coupling and enhances the stability of synthesized oligonucleotides, contributing to a range of molecular biology applications. -
Phosphoramidite Derivative
GalNAc-NAG15 phosphoramidite is a phosphoramidite derivative featuring N-acetylgalactosamine (GalNAc) linked to N-acetylglucosamine (NAG). This compound serves as a key building block for the synthesis of oligonucleotides, enabling the incorporation of GalNAc for applications in glycobiology and gene delivery research. Its unique structural properties facilitate the study of glycan interactions and the development of glyco-engineered therapeutics. -
Phosphoramidite Derivative
GalNAc-NAG25 phosphoramidite is a phosphoramidite derivative featuring N-acetylgalactosamine (GalNAc) linked to N-acetylglucosamine (NAG). This compound is primarily utilized in the synthesis of oligonucleotides, enabling the incorporation of glycosylated structures into nucleic acid sequences. Its application is significant in the study of glycobiology and the development of nucleotide-based therapeutics. -
Phosphoramidite Derivative
GalNAc-THA C6 phosphoramidite is a phosphoramidite derivative that features N-acetylgalactosamine (GalNAc) connected to a Trishexylamino (THA) moiety. This compound serves as a building block in the synthesis of oligonucleotides, enabling the incorporation of glycan structures for various molecular biology applications. Its unique properties facilitate studies in gene expression, RNA interactions, and therapeutic oligonucleotide development. -
Phosphoramidite Compound
3'-NH-Tr-2',3'-dT-5'-CE-Phosphoramidite is a phosphoramidite compound utilized in the synthesis of oligonucleotides and nucleic acid analogs. It plays a crucial role in the development of antiviral and anticancer research applications. This reagent facilitates the incorporation of modified nucleotides, enabling the exploration of therapeutic strategies in nucleic acid-based interventions.
