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Short description of different protein analysis / characterisation methods as Edman-Sequencing, Intact Mass Determination, Amino acid analysis, Post-translational Modifications or Disulfide Bridge Analysis.
Standard PCR amplification once required often laborious DNA extraction, purification, end-stage processing and sample set-ups, using relatively primitive instruments and complex protocols. The notion that 35 cycles of PCR amplification could be completed in under 25 minutes, without compromising precision or accuracy, was considered a distant prospect.
SNP PolTaq DNA polymerase for better Sake taste and flavor: SNP PolTaq for qPCR for the unambiguous identification of point mutations in yeast!
Read more about a recent case report from Japan.
Point mutations are the cause of many hereditary diseases and are considered risk factors, for example, for Alzheimer's Disease.
One of the main causes of many hereditary diseases could not be resolved precisely enough by mid-2016, even with the "super tool" CRISPR / Cas9: the point mutation.

Sustainability at Genaxxon

We at Genaxxon bioscience are aware of our corporate responsibility. Our philosophy is to practice sustainability whenever possible. The following are some examples of the many changes that we have implemented successfully.
Nowadays there are many different suppliers and systems for polymerase chain reaction (PCR) and of its derivative techniques, quantitative, or real-time, PCR (qPCR) and reverse transcription PCR (RT-PCR). Competition gives you the opportunity to simplify diagnostics and to make research more financially favorable.
We are proud to inform you that Genaxxon bioscience has been successfully certified according TÜV ISO 9001: 2015!

PCR Beads Ready-To-Use lyophilized - LyoBeads:

Get the same reliable performance in your realtime PCR as before, now with a two-year shelf life at room temperature!

Pre-formulated, freeze-dried realtime PCR master mix in bead format. No need to store the PCR Master Mix (Beads) in the refrigerator or freezer. No unnecessary freeze-thaw cycles. No wasted time for thawing the master mix each time!
The qPCR and Digital PCR Conference started with lectures on the reliability of qPCR and ddPCR, from their technical limitations to the interpretation of results to errors in published data with a very interesting presentation by Prof. Stephen Bustin.

miRNAs in Gene Expression

miRNAs occur naturally in animal and plant organisms. They are highly conserved and play an important role in gene regulation, especially in gene silencing. They have an important function in cell differentiation and dedifferentiation, for example in female fertility and preimplantation development.

Digital PCR (dPCR)

Doing digital PCR means to carry out a PCR reaction with only one single amplification step nonetheless resulting in absolute/quantitative values. For dPCR, in contrast to conventional real-time PCR (qPCR), no standard curves, calculating of Ct-values or standard references are required because the single amplification step is performed to obtain a pure yes (positive) or no (negative) answer.

Citations in Scientific Literature

In the articles below you will find the authors already relying on the Genaxxon products. We say thank you to these authors, trusting in our service. Let us convince you as well.
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