Reverse Transcriptases & RT-PCR
Reverse transcription, enables researchers to study RNA with the same molecular approaches used for DNA investigations. cDNA generated by reverse transcription can be amplified using polymerase chain reaction (PCR). NEB offers several reagents for cDNA Synthesis for use in applications including qPCR and qRT-PCR. For your convenience, reagents are available as kits or standalone products, depending on your needs.
Choose Type:
Protocols for Reverse Transcriptases & RT-PCR
- Loop-mediated Isothermal Amplification (LAMP)
- First Strand cDNA Synthesis Protocols (E6560)
- Reaction Conditions (E5315)
- Standard PCR Protocol (E5315)
- One-Step RT-PCR Protocols (E5315)
- Typical RT-LAMP Protocol
- Typical cDNA Synthesis Protocol
- First Strand cDNA Synthesis (Standard Protocol) (NEB #M0253)
- First Strand cDNA Synthesis (Standard Protocol) (NEB #M0368)
- First Strand cDNA Synthesis (Quick Protocol) (NEB #M0368)
- First Strand cDNA Synthesis (No-RT Negative Control Reaction) (NEB #M0253)
- First Strand cDNA Synthesis (No-RT Negative Control Reaction) (NEB #M0368)
- First Strand cDNA Synthesis (Quick Protocol) (NEB #M0253)
- First Strand cDNA Synthesis (Standard Protocol) (NEB #M0277)
- First Strand cDNA Synthesis (No-RT Negative Control Reaction) (NEB #M0277)
- First Strand cDNA Synthesis Protocols (E6300)
- First Strand cDNA Synthesis (Quick Protocol) (NEB #M0277)
- PCR Amplification with OneTaq® RT-PCR Kit
- First strand cDNA synthesis OneTaq® RT-PCR Kit
- Protocol for NEBNext® Ultra™ II Non-Directional RNA Second Strand Synthesis Module (E6111)
- Avoiding Ribonuclease Contamination
Other Tools & Resources
Usage Guidelines
Reagents for RNA Sample Preparation
RNA Polymerase Selection Chart
RNA Ligase Selection Chart
cDNA Synthesis Selection Chart
