Evo M-MLV One Step RT-qPCR Kit (SYBR Method) Ver.2

Product Code: AG11732

- +

¥1,800

Product Description

This product is a specialized kit for One Step RT-qPCR using SYBR Green I chimeric fluorescence method. Reverse transcription and qPCR reactions are completed in the same tube, which is simple and fast to operate and can effectively reduce the risk of contamination. The product utilizes a high elongation capacity Evo M-MLV Reverse transcriptase, integrated hot start Pro Taq With the superior performance of HS, it is widely applicable to the amplification of various templates, and can be used to efficiently synthesize cDNA and efficiently and stably amplify qPCR in a short period of time.

Product Advantages

① This is a one-step RT-qPCR reaction kit, which completes the reverse transcription and qPCR reaction in a single tube, simplifying the operation, improving the efficiency, and effectively reducing the possibility of contamination by multiple operations.
②This product adopts a strong extension ability Evo M-MLV Reverse transcriptase, high performance hot start enzyme Pro Taq HS and optimized reaction system with high specificity and amplification efficiency.
③ This product can detect trace amounts of RNA quickly and accurately.

Product Composition
individual parts making up a compound norm
2X One Step RT-qPCR Buffer II (SYBR)*1 1.25 ml x 2 pcs
One Step Enzyme Mix II *2 200 μl
RNase free water 1 ml x 3 pcs

*1: This solution contains dNTP Mixture, Reaction Buffer, and SYBR dye, store away from light.
* :: 2: Contains Evo M-MLV RTase, RNase Inhibitor.Pro Taq HS DNA Polymerase.

Preservation and transportation
Storage temperature: -20℃ [2X One Step RT-qPCR Buffer II (SYBR) should be stored away from light.
Transportation temperature: dry ice transportation or -20℃ ice bag transportation.
Example 1

Mouse Total RNA (100 ng ~ 100 fg) was used as a template for One Step RT-qPCR using this kit. ApoE Gene.

The results are shown above:
① Amplification efficiency was 96%, R2= 0.9998;
② Accurate quantification can be performed over a wide template range, and the amplification curves of RT-qPCR reactions with 100 ng ~ 100 fg Total RNA show good linearity.
③ The melting curve has a single peak type, no spurious peaks, and strong amplification specificity.