Notice: wp_enqueue_style was called incorrectly. Scripts and styles should not be registered or enqueued until the wp_enqueue_scripts, admin_enqueue_scripts, or login_enqueue_scripts hooks. This notice was triggered by the font-awesome handle. Please see Debugging in WordPress for more information. (This message was added in version 3.3.0.) in /var/www/vhosts/ on line 5311

Notice: Undefined index: pll_language in /var/www/vhosts/ on line 138
FastGene Scriptase II cDNA Kit | NIPPON Genetics EUROPE

Ligation of DNA strands

FastGene Scriptase II cDNA Kit

Catalogue number: LS63

FastGene® Scriptase II cDNA Kit (100 rxns) contains FastGene Scriptase II, enzyme buffer, dNTPs, Oligo dTs, random hexamers and RNase inhibitor

Engineered enzyme

Engineered reverse transcriptases allowed the synthesis of cDNA from very low amounts of RNA. Mutations are inserted into the RNase H domain of the MuLV‘s reverse transcriptase. Therefore, by not degrading the RNA during the first-strand synthesis, a higher yield of full-length cDNA is obtained. Additionally, a higher thermal stability increases the robustness of the enzyme. The FastGene® Scriptase II is exactly one of those engineered enzymes. With its mutation in the RNase H domain and higher thermal stability, it is the optimal choice for more complex applications, such as RT-qPCR and NGS.


  • Quantification of Gene Expression
  • RT-qPCR
  • Next Generation Sequencing
  • Low RNA concentration
  • Difficult templates

Lower RNase H activity for longer cDNA

The FastGene® Scriptase II has a modified RNase H domain. The RNA is therefore not degraded and serves as a template for longer cDNAs, resulting in fragment size of up to 12 kBp.

Engineered enzymes – optimized for qPCR

The FastGene® Scriptase II delivers superior cDNA templates for downstream applications, e.g. qPCR and NGS. The resulting full-length cDNA gives a complete picture of the gene and is able to show modification, e.g. splicing variants.

Comparison of different PCR results

Multiplex PCR

Fig. 1: Comparison of multiplex PCR using cDNA produced by Competitor I‘s SS-II enzyme and FastGene® Scriptase II at 42 °C and 50 °C.


Fig. 2: Comparison of qPCR results using primers for GAPDH and cDNA produced by using different RNA starting concentration by Competitor I‘s SS-II enzyme   and FastGene® Scriptase II at 42 °C.

Fig. 3: Comparison of qPCR results using primers for YWHAZ and cDNA produced by using different RNA starting concentration by Competitor I‘s SS-II enzyme and FastGene® Scriptase II at 42 °C.

Manual for the FastGene Scriptase II cDNA Kit
Application Note
Comparative study of reverse transcriptase reaction using RNA extracted from zebrafish fertilized eggs
Technical Note
Very fast reverse transcription reactions (5min)
Application Note
Reverse transcriptase reaction for quantitative expression analysis using RNA extracted from mesenteric adipose rat tissue
Application Note
Comparative study of RT-reaction by using RNA extracted from mouse lymph node
Application Note
Comparative study of reverse transcriptase reaction using RNA extracted from peritoneal cells of sterile peritonitis model mouse
Application Note
Cloning of isoflavone biosynthesis related enzyme using RNA extracted from soybean

Which concentration of gene specific primer for LS63 is recommended?

We recommend to use 15 pmol – 20 pmol for gene specific primer

What is the purpose of the step 42°C for 2 minutes and will the yield decrease significantly if I skip this step? If I use oligo dT primer can I skip this step?

The purpose of this step is the annealing of primer. For oligo dT it is basically recommended to have an annealing step at 42°C for 2 minutes, because it has low Tm.

The yield is not influencend if the amount of template is sufficient and the primers work well (good designed). In this case you can skip the step. But if the amount of template is small and the primer are not optimized we expect that there will be an effect to the yield.

In the protocol the annealing step for oligo dT is a standard recommendation. For certain targets, the condition of 40°C for 2 minutes or 37°C for 2 min and so on, could be better for real time experiments than 42°C. This means it is possible that you need to optimize empirically the reaction temperature, time and step for your target.

Can I use the Scriptase II cDNA Kit with a high amount of RNA (2.5 µg per 20 µl)?

We recommend a max of 1 µg. Reason: the highly expressed genes will over proportionally be represented in such high concentration. Meaning the chances of finding a high-concentrated mRNA is much higher than a low concentrated one. If you stick to 1 µg, the amount of enzyme to mRNA will be much higher, guaranteeing the complete RT of all mRNA.

Is this Enzyme influenced by DEPC?

If DEPC is not completely removed, it can inhibit all enzymatic reactions including Scriptase II.

on 07/12/2018

I especially like that the Scriptase II lead to stable results. As a result of performing RT-PCR using tumor derived RNA, we were able to detect the expression of genes whose amplification was unstable with other RT reagents. The Amplification of full-length cDNA has also been confirmed. I would love to also try the 5x Ready Mix.

on 05/17/2018

PCR amplified DNA fragement was cloned into a vector and the sequence was confirmed. As a result, there was no artificial mutation such as changes of single nucleotides.

Also, the manual of your product (FastGene® Scriptase II cDNA Synthesis Kit) was very easy to understand and I felt no stress on the operation. I definitely want to use other products from NIPPON Genetics.

on 12/21/2017

"The FastGene® scriptase II cdna synthesis kit appeared to be a reliable method to perform RT-PCR experiments using induced sputum samples which is a difficult specimen matrix. Indeed, it allowed to obtain a good reproducibility and good amplification curve profils. Furthermore, the cost of this product is really cheap compared to what we use to buy."

Translation by Nippon Genetics:

Das FastGene® Scriptase II cDNA Kit zeichnet sich als zuverlässige Methode aus um RT-PCR Experimente mit Proben eines induzierten Suptums durchzuführen. Obwohl dies eine schwere Probenmatrix ist, konnte eine gute Reproduzierbarkeit und ein gutes Amplifikationskurvenprofil gewonnen werden. Zusätzlich sind die Kosten verglichen zu dem zuvor verwendetem Produkt sehr preisgünstig.

on 09/27/2017

“We have tested the RT kit FastGene Scriptase II in comparison with other kits, like Protoscript II (NEB) and Superscipt II (Invitrogen) and we have noted that the results are similar. Additionally, we can make more “runs” for a better price!”
Overall Customer Rating


Thank you very much for your rating.
Add a review for "FastGene Scriptase II cDNA Kit"
Please confirm recaptcha. Please rate the product. Please make sure you have filled all fields correctly. Please accept our privacy policy terms.