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

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

An improved version of SuperScript RT

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)

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

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

Offers highest sensitivity for end point detection

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)

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

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

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

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

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

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

Supplied at 5X concentration

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

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

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

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

Amplifies RNA targets up to 9.0kb

Designed to effectively suppress background fluorescence in live cell assays

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

No endonuclease activity and extremely low RNase H activity

Kit design eliminates need to perform large-scale RNA preparations and Northern blots

For reverse transcription of RNA into double-stranded cDNA products