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    In the spring, we will participate in the 1st Czechoslovak Congress of Medical Genetics, which will take place from April 2–4, 2025, at the Cultural and Congress Center Elektra in the spa town of Luha...

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  • RANK 2025

    Visit us at the 19th edition of the RANK 2025 conference, which will take place on March 19th and 20th at the Zlatá Štika Hotel in Pardubice. The conference is organized by the Czech Society of Clinic...

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  • Kapras Day 2025

    We would like to invite you to the 23rd Kapras Day on the topic of  "Clinical Genetics," which will take place on Wednesday, February 26, 2025, in the Congress Hall of Hotel Olšanka in Prague. We loo...

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RNA Contamination Removal Beads (gDNA Purification)

Contact us

40060

gDNA purification

95% efficiency

removal of RNA

Description:

Magnetic beads for genomic DNA (gDNA) purification from the American company BioDynami combine BioDynami's patented chemistry with the unique properties of SPRI beads (Solid Phase Reversible Immobilization). They effectively eliminate contaminating RNA and recover gDNA in a single reaction step. Additionally, unwanted components such as proteins, dNTPs, salts, enzymes, and other impurities can also be removed in the same step. The genomic DNA is then ready for downstream applications such as PCR, qPCR, sequencing, and enzymatic processing, etc.

 

Workflow:

In the first step (gDNA Binding RNA depletion), genomic DNA binds to the magnetic beads while RNA is simultaneously removed. This is followed by magnetic separation (Magnetic Separation), where the beads with bound DNA are captured using a magnet, and unwanted contaminants are removed. In the washing step (Washing), the beads are washed to remove any remaining impurities. Finally, in the elution step (Elution), the purified genomic DNA is released from the beads into the elution buffer.

RNA contamination removal

 

Efficiency:

The graph on the left shows the yield of genomic DNA before (Input) and after (Purified) purification, with the magnetic bead purification maintaining a high DNA recovery rate. The electrophoretic gel on the right demonstrates the presence (Purification +) and absence (Purification -) of RNA contamination in the DNA sample after purification. It shows that after purification with magnetic beads, RNA is effectively removed, resulting in clean genomic DNA suitable for downstream applications.

RNA Contamination Removal

 

Features:

  • Effective removal of RNA contamination by RNase
  • Removal of unwanted components and impurities
  • High recovery rate of genomic DNA


Package size:

40 reactions (Cat. No. 40060S)
200 reactions (Cat. No. 40060L)

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