Magnetic FFPE DNA Extraction Kit, 1 pack = 250 T

Magnetic FFPE DNA Extraction Kit(Prepackaged), 1 pack = 96 T

This DNA extraction is performed in 2 ml microfuge tubes. The superior co-precipitating reagents do not interfere with qPCR and ensure that pellets do not become dislodged during the extraction procedure. This eliminates the need for both centrifuging the samples again or repeating a run. Also, since the kit does not use iodine or glycogen your clothes will be stain-free! The kit provides reagents sufficient for analysis of 50 samples in duplicate.

This DNA extraction is performed in a 96 deep-well plate, a convenient high-throughput format that allows you to process up to 96 samples or multiple plates in the same run. Use multichannel pipettors to increase efficiency and decrease repetitive handling while minimizing mistakes associated with handling individual tubes. The proprietary co-precipitating reagent used in the kit keeps the pellet seated in the well and does not interfere with qPCR. Also, since the kit does not use iodine or glycogen, your clothes will be stain-free! Each kit has reagent sufficient for 96 individual extractions in less than 2 hours.

This DNA extraction buffer is for use with wells, 30 ml

This DNA extraction buffer is for use with tubes, 30 ml

Genomic DNA Extraction Mini spin column kit is a research kit used for isolation of genomic DNA. The kit combines the selective binding properties of a silica gel- based membrane, with the speed of micro spin. The sample is lysed under highly denaturing conditions, to ensure release of intact DNA. Buffering conditions are then adjusted to provide optimum binding of the DNA to the column and the sample is loaded on to a spin column. The DNA binds to the membrane and contaminants are efficiently washed away using two different wash buffers. High quality DNA is eluted in a special buffer, ready for direct usage and storage.

Plant DNA Extraction Kit is a quick, inexpensive, and consistent protocol toextract high-quality DNA with better yield. The silica spin column technologyallows for recovery of high quality nucleic acids from fresh, preserved or frozensamples. The kit combines the selective binding properties of a silica gel- basedmembrane, with the speed of micro spin. The sample is lysed under highlydenaturing conditions, to ensure release of intact DNA. Buffering conditions arethen adjusted to provide optimum binding of the DNA to the column and thesample is loaded on to a spin column.The DNA binds to the membrane and contaminants are efficiently washed awayusing two different wash buffers. High quality DNA is eluted in a special buffer, ready for direct usage and storage.

The overall goal is to isolate chromosomal DNA from leaves. The extraction buffer breaks the cell walls to release the cellular constituents. The buffer contains a detergent cetyl methylammonium bromide (CTAB) that disrupts the cellular membranes to release the DNA, EDTA which minimizes nuclease activity and NaCl that removes polysaccharide. The contaminating RNA is removed by digestion with RNase A. Finally, nucleic acids are precipitated in water-alcohol mixture.

An excellent tool to purify plasmid DNA from bacterial cultures swiftly. Based on the DNA binding to silica-based membranes in chaotropic salts. The Kit shortens the handling time to about 30 min. The high quality plasmid DNA can be used directly for any downstream applications

Tissue DNA Extraction Mini kit is a research kit used for isolation of DNA from a wide variety of tissue specimens. The kit combines the selective binding properties of a silica gel- based membrane, with the speed of micro spin. The sample is lysed under highly denaturing conditions, to ensure release of intact DNA. Buffering conditions are then adjusted to provide optimum binding of the DNA to the column and the sample is loaded on to a spin column. The DNA binds to the membrane and contaminants are efficiently washed away using two different wash buffers. High quality DNA is eluted in a special buffer, ready for direct usage and storage. The Purified DNA is free of protein, nucleases and other contaminants and inhibitors

The overall goal is to isolate chromosomal DNA from bacterial cells. The cells are first re-suspended in a suitable buffer (that minimizes nuclease activity) and ruptured to release the cellular contents. The contaminating RNA is removed by digestion with RNase A. Finally, nucleic acid is precipitated in water-alcohol mixture in presence of high concentration of inorganic salt

Whole Blood DNA extraction kit provides a fast, easy method to purify Genomic DNA for downstream processes. Genomic DNA can be purified from the whole blood that is treated with anticoagulants other than heparin. The kit combines the selective binding properties of silica gel-based membrane, with the speed of microspin. The sample is lysed under highly denaturing conditions, to ensure release of intact DNA. Buffering conditions are adjusted to provide optimum binding of the DNA to the column and the sample is loaded on to a spin column. DNA binds to the membrane and the contaminants are efficiently washed away using two different wash buffers. High quality pure DNA is eluted in a special buffer, ready for immediate use or storage.

PurePlasmid DNA Maxi Extraction Kit, 1 pack = 10 T

Endo-free Plasmid DNA Mini Extraction Kit, 1 pack = 50 T

Endo-free Plasmid DNA Mini Extraction Kit, 1 pack = 100 T

Endo-free Plasmid DNA Midi Extraction Kit, 1 pack = 50 T

N96 Endo-free Plasmid DNA Mini Extraction Kit, 1 pack = 96 T

N96 Endo-free Plasmid DNA Mini Extraction Kit, 1 pack = 96 Tx4

Endo-free Plasmid DNA Maxi Extraction Kit, 1 pack = 10T