Products & Reviews

CPG for incorporation of an (otherwise unmodified) reverse (5' to 3') dT nucleobase at the 3' end of an oligonucleotide.  

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CPG used to add the non-fluorescent quencher BHQ-1 dye to the 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for the incorporation of a 2'-fluoro modified nucleobase at the 3' end of an oligonucleotide

CPG for the incorporation of an (otherwise unmodified) reverse (5' to 3') nucleobase at the 3' end of an oligonucleotide.

CPG used to incorporate the cyanine-5 dye moiety onto the 3'-end of an oligonucleotide.

CPG used to incorporate a methyl-dC ROX-phosphate moiety into the 3' end of an oligonucleotide.

A phosphoramidite used for 5'-CAL Fluor Red 610 labelling of oligonucleotides.

CPG for the incorporation of a 2'-O-methyl modified ribo-A nucleobase at the 3' end of an oligonucleotide.

CPG for incorporation of a 2'-O-methyl modified ribo-C nucleobase at the 3' end of an oligonucleotide.

CPG for incorporation of unmodified ribo-G at 3' end of an oligonucleotide.

CPG for incorporation of a 2'-O-methyl modified U nucleobase at the 3' end of an oligonucleotide.

CPG for incorporation of GalNAc at 3' end of an oligonucleotide, with a dR spacer.

CPG for the incorporation of cholesterol at 3' end of an oligonucleotide, with a dR spacer.

Helps simplify inventory, reduce costs, and improve efficiencies

Assists in the documentation of calibration verification and linearity

Helps labs to avoid false-negative and false-positive results

T7 RNA Polymerase catalyzes the 5′→3′ RNA synthesis from the T7 promoter. It is a DNA-dependent RNA polymerase cloned from the T7 bacteriophage, which recognizes the T7 promoter and terminator sequences with high specificity. Key features:  Reliable transcription