LGC Biosearch Technologies Products & Reviews

You know what you’re looking for and we’re here to help you find it. Our highly qualified molecular biologists and PCR assay design experts act as an extension of your team, designing the best qPCR assay for your target of interest and experimental conditions.  

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 a 2'-O-methyl modified ribo- 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.

Ribonuclease R (RNase R) from E. coli is a magnesium-dependent 3ʹ to 5ʹ exoribonuclease available for circular RNA cleanup, alternative splicing research, and gene expression studies.  Key features:  Efficacy and quality assured under ISO 13485 certification Available in bulk and for custom configurations Effectively degrades linear RNA, Y-structure RNAs, but not lariat loops or circular RNAs Digests linear RNAs…

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 

Protect RNA with this high quality, effective RNase inhibitor.

Degrade dsDNA and ssDNA , digest unwanted DNA without digesting RNA, use in a variety of applications from IVT transcription to RT-PCR