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- Nucleic Acid Analysis
- Protein Analysis
- Biochemical Reagents
-
Enzymes
- Thermophilic DNA Polymerases
- Mesophilic DNA Polymerases
- Restriction Endonucleases
- Reverse Transcriptase and RNA Polymerases
- DNA/RNA Ligases
- RNases
- Proteases
- Nucleases
- Kinases
- Phosphatases and Sulfurylases
- DNA Repair Proteins
- Single-Stranded DNA Binding Proteins
- Chaperon Proteins and Disulfide Bond Isomerase
- Others
- Gene editing
- Molecular cloning
- Clinical diagnostics
- Human Identification STR kits
- Laboratory instruments
- Software
- A&A Biotechnology
News
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1st Czechoslovak Congress of Medical Genetics 2025
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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PRODUCT HIGHLIGHTS
- Suitable for the simultaneous
processing of multiple samples
- No need for organic extractions
- No need for time-consuming
alcohol precipitations
- Immediate inactivation of exogenous
and endogenous RNases
- Favored binding of RNA
molecules > 200 bases
- Efficient separation of enzyme
inhibitors and contaminants
- Final elution in RNase free water
- Two types of columns for increased
sample and user protection or easy
handling
PRINCIPLE
The peqGOLD Total RNA Kit uses the
reversible binding properties of the
silica based PerfectBind RNA Column.
Samples are first lysed under denaturing
conditions. The lysate is then applied to
the PerfectBind column. The Total RNA
selectively binds to the silica matrix, can
then be washed and eluted with RNase
free water at the end.
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