You searched for: RNA Synthesis and Transcription
TriLink® CleanScribe™ RNA Polymerase
Supplier: TriLink BioTechnologies
CleanScribe™ RNA Polymerase is a novel enzyme that reduces double-stranded RNA (dsRNA) formation in IVT RNA synthesis.
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TriLink® T7 RNA Polymerase
Supplier: TriLink BioTechnologies
T7 RNA Polymerase is a wild-type enzyme to synthesize RNA from DNA templates by in vitro transcription.
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TriLink® CleanCap® Reagent AG (3'OMe)
Supplier: TriLink BioTechnologies
TriLink's patented CleanCap® Reagent AG (3' OMe) is a co-transcriptional capping reagent for in vitro transcription of 5' capped mRNA resulting in a Cap 1 structure with >95% capping efficiency.
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T7 RNA polymerase
Supplier: Thermo Fisher Scientific
T7 RNA polymerase is ideal for synthesis of unlabeled and labeled RNA. It catalyses the 5'→3' synthesis of RNA on either single-stranded DNA or double-stranded DNA downstream from it promoter. It is also used in the study of RNA secondary structure and RNA-protein interactions, RNA splicing.
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TriLink® Inorganic Pyrophosphatase (iPPase)
Supplier: TriLink BioTechnologies
Inorganic Pyrophosphatase (iPPase) is an enzyme to remove pyrophosphate in IVT to drive the reaction forward.
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TriLink® CleanCap® Reagent AG
Supplier: TriLink BioTechnologies
CleanCap® Reagent AG is TriLink’s patented co-transcriptional capping reagent for in vitro transcription of 5’ capped mRNA resulting in a Cap 1 structure. CleanCap has shown to provide up to 98% capping efficiency.
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TriLink® Engineered RNase Inhibitor
Supplier: TriLink BioTechnologies
Engineered RNase Inhibitor is a protein to inhibit RNase activities to prevent RNA degradation in IVT.
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TriLink® CleanCap® Reagent AU
Supplier: TriLink BioTechnologies
CleanCap® Reagent AU is designed for the co-transcriptional capping of self-replicating or self-amplifying (saRNA) to produce an optimal Cap 1.
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TriLink® CleanCap® Reagent M6
Supplier: TriLink BioTechnologies
TriLink's patented CleanCap® Reagent M6 [CleanCap m6AG (3′ OMe)], is designed for the co-transcriptional capping of mRNA to produce an mRNA with base-modified Cap 1. Cap-1 mRNAs have superior in vivo activity compared to Cap-0 mRNAs produced by legacy capping methods.