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

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

Optimized for generating first-strand cDNA from total or poly(A)+ RNA

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

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

Combines the high performance of Invitrogen Cloned AMV RT with the convenience of optimized, prequalified reagents

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

An avian RT with reduced RNase H activity designed for RT-PCR

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

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

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

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)

Amplifies RNA targets up to 9.0kb

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

For reverse transcription of RNA into double-stranded cDNA products

Commonly used in the first step of RT-PCR as well as for primer extension experiments

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

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)

Supplied at 5X concentration

Can be used to synthesize first-strand cDNA for amplification by PCR or for cloning subsequent to conversion to double-stranded cDNA

Offers highest sensitivity for end point detection

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

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

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