Optimized to synthesize first-strand cDNA from purified poly(A)⁺ or total RNA or RT-PCR

Delivers extremely high-quality, single-stranded cDNA from 0.02 to 2μg total RNA

Proprietary mutant of SuperScript II RT

An improved version of SuperScript RT

Designed for optimum performance with TaqMan Gene Expression Master Mix, Power SYBR™ Green PCR Master Mix, and other PCR enzymes

Designed for sensitive, reproducible, end-point detection and analysis of RNA molecules by RT-PCR

Provides the high-temperature capability of SuperScript III Reverse Transcriptase (RT) in an optimized format for generating first-strand cDNA for use in real-time quantitative RT-PCR (qRT-PCR)

Delivers extremely high-quality, single-stranded cDNA from 0.02 to 2μg total RNA

Optimized SuperMix formulation for first-strand cDNA synthesis from purified poly(A)+ or total RNA

Offers highest sensitivity for end point detection

Recombinant DNA polymerase that synthesizes a complementary DNA strand from single-stranded RNA, DNA, or an RNA:DNA hybrid

For use with reverse transcriptase-PCR (RT-PCR)

Optimized to synthesize first-strand cDNA from purified poly(A)+ or total RNA

A recombinant moloney murine leukemia virus (rMoMuLV) reverse transcriptase that has been optimized for TaqMan-based assays

Convenient 2X format allows further addition of template and primer at any desired concentration

Supplied at 5X concentration

Optimized for researchers performing RNA structure, RNA sequencing, protein footprinting, and boundary experiments. Invitrogen™ Ambion™ RNase T1 (1U/μL) includes RNase T1, 10X RNA Structure Buffer, 1X Alkaline Hydrolysis Buffer, Yeast RNA, Precipitation/Inactivation Buffer and Gel Loading Buffer II.

High-purity enzyme that's a mix of cloned RNA polymerase and RNase inhibitor

Amplifies RNA targets up to 9.0kb

Catalyzes the addition of adenosine to the 3' end of RNA in a sequence-independent fashion

Designed to effectively suppress background fluorescence in live cell assays

A cloned high-purity RNA polymerase with a high specificity for its promoter

Makes it possible to perform expression analysis directly from cultured cells without RNA purification

Catalyzes formation of a phosphodiester linkage between a 5'-phosphoryl-terminated nucleic acid donor and a 3'-hydroxyl-terminated nucleic acid acceptor

A buffered nonionic detergent solution for the lysis of adherent or nonadherent cultured cells under non-denaturing conditions

Provides the high-temperature capability of SuperScript III Reverse Transcriptase in an optimized SuperMix format for synthesis of first-strand cDNA for use in real-time quantitative RT-PCR (qRT-PCR)