| eAMV has superior performance and thermal stability |
| Sensitivity for low abundance message is critical for comparative gene expression studies. eAMV has superior processivity and thermal stability compared to other reverse transcriptases. These unique features make it the ideal enzyme for detection of low abundance RNA, especially those with difficult secondary structure. |
| Figure 1. RT-PCR was performed on total RNA-HELA cells serially diluted from 1000 ng to 1 ng. Reactions were performed with b actin primers according to suppliers' protocols. |
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Lanes 1, 10, 11, 20: PCR Marker Lanes 2, 6, 12, 16: 1000 ng Lanes 3, 7, 13, 17: 100 ng Lanes 4, 8, 14, 18: 10 ng Lanes 5, 9, 15, 19: 1 ng
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| Enhanced sensitivity and specificity with JumpStart Taq DNA Polymerase |
| The addition of JumpStart antibody to the PCR mix increases sensitivity and specificity of PCR amplification in both the one-step or two-step reactions. |
| Figure 2. RT-PCR amplification of a 440 bp fragment from tobacco mosaic virus RNA template was performed using the one-step protocol. |
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Lane 1: DNA ladder Lanes 2 & 3: 2 ng starting RNA Lanes 4 & 5: 200 pg starting RNA Lanes 6-7: 20 pg starting RNA |
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