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The kit uses the technology of DNA sorption on magnetic particles. The entire DNA extraction process combines the steps of sample lysis, subsequent selective binding of the released DNA to magnetic beads, and then, after a series of washes, elution with the option of concentrating the DNA in a low-salt buffer.
Benefits of the set:

• High yield of genomic DNA from E.coli and eukaryotic cells: 4-5 µg DNA from 0.5-1*109 bacterial cells and 0.25-1*106 eukaryotic cells.
• High yield of genomic DNA when isolated from various mouse tissues and organs.
• Indicators A260/280 = 1.80±0.05, A260/230 ≥ 2.1
• Purified DNA is verified to be free of proteins, nucleases or other contaminants and can be used in a wide range of molecular biology techniques such as PCR, RT-PCR or other enzyme reactions.
• High throughput for DNA extraction from large numbers of samples.

a set of reagents for the secretion of nucleic acids (DNA/RNA) from biological material by sorption on magnetic particles. Compatible biomaterial: • Smears from the upper respiratory tract • Buccal epithelium • Saliva • Fecal extracts • Whole blood • Blood plasma

The dNTP mixture is an aqueous solution of four highly purified 2’-deoxynucleoside-5’-triphosphates (dATP, dTTP, dHTF, dCTF) in equimolar concentration

Genta-ExoI exonuclease I hydrolyzes single-stranded DNA in the 3'→ 5' direction, releasing deoxyribonucleoside 5'-monophosphate. It does not cleave DNA chains whose 3’-end is blocked by a phosphoryl or acetyl group. Active in the PCR buffer. Isolated from a strain of Escherichia coli expressing the exonuclease I gene of E.coli.

The polymer provides single-nucleotide separation of fragments of the Sanger DNA sequencing reaction in the range from 20 to 1000 nucleotides as part of genetic analyzers operating on the principle of capillary gel electrophoresis, for example, Nanofor 05

The ALSENSE Forensic reagent kit is designed to determine and evaluate the amount of human genomic DNA and gender by real-time polymerase chain reaction in human biological material. The reagent kit is intended for use in criminology, as well as PCR research in biology and medicine. The reagent kit is based on the polymerase chain reaction method with hybridization-fluorescence detection in real time (PCR-RV) using specific TaqMan probes. Amplification of multi-copy autosomal fragments of different sizes allows for a reliable assessment of the amount of DNA in the sample under study, and amplification of a multi-copy fragment of the Y chromosome to determine gender.

Medicines may contain pyrogens, the sources of which can be bacteria, viruses, fungi, and pyrogens can also be by-products of the production process. Contamination of drugs with pyrogenic substances is a serious threat to the health of patients and can lead to the development of fever and, ultimately, shock and death. Currently, to determine the content of pyrogenic substances (bacterial endotoxins and substances of non-endotoxin nature), the “Pyrogenicity” test is used, carried out on rabbits, which is inaccurate and harmful to animals. The monocyte activation test (MAT) has higher sensitivity and does not require the use of animals.