ForeDirect RT-qPCR Kit

◮ For RNA direct real-time amplification from swab collections without RNA purification processes. This kit completes the qRT-PCR cycles within one hour. The enzyme mix is an optimized blend of Reverse Transcriptase, Hot-Start Taq DNA polymerase, RNase inhibitor. The Reaction Buffer contains all of the required components, including optimized buffer components, Mg2+, dUTP, and dNTPs. foregene strength

Products Details

100T1. Once the PCR reaction tubes have been briefly centrifuged, place them in the sample tank of amplification instrument. 2. Thermal protocol

Step

Temperature

Time

Cycles

1

Reverse transcription

50℃

15 mins

1

2

Pre-denaturation

95℃

1 min

1

3

Denaturation

95℃

10 seconds

42

4

Anneal/Extension

60℃

30 seconds

Note: Fluorescent signal was detected immediately after the extension step of each cycle. 3. After setting, save the file and run the reaction program.
 Nucleic acid release agent
 RNA protectant
 2× RT-qPCR Buffer
 Enzyme Mixture(Taq&M-MLV)

Instructions

-The kit should be stored at -20 ± 5. The validity period is 12 months. -Avoid repeated freeze-thaw cycles (<5 cycles).Before reagent preparation, all the reagents in the kit should be thawed at room temperature and mixed gently.   Reagent preparation 1. Prepare the Nucleic Acid Release Mix

Component

Volume per Sample or Control

Nucleic acid release agent

5μL

RNA protectant

0.5 μL

2. Prepare the Reaction Mix

Component

Volume per Sample or Control

2× RT-qPCR Buffer

15 μL

Enzyme Mixture(Taq&M-MLV)

1.5 μL

Primers and Probes

1μL

ForeDirect RT-qPCR Kit is designed for RNA direct real-time amplification from swab collections without RNA purification processes. This kit completes the qRT-PCR cycles within one hour. The enzyme mix is an optimized blend of Reverse Transcriptase, Hot-Start Taq DNA polymerase, RNase inhibitor. The Reaction Buffer contains all of the required components, including optimized buffer components, Mg2+, dUTP, and dNTPs.

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