Molecular Biology Products

accessories, buffers & reagents

G-Biosciences offers a wide selection of accessories, buffers and reagents used in molecular biology processes, including:

DNA OUT™
DNA OUT™ is formulated to quickly remove DNA and RNA contaminations from glass and plastic wares. Simply spray and rinse. DNA OUT™ is non-toxic and leaves no Online Storeresidues to interfere with downstream applications. The fast acting DNA OUT™ allows laboratory equipment and work areas to be made free from DNA contamination.

Ideal for cleaning microfuge tubes, reaction tubes, PCR machine surface, pipettes, lab benches, lab equipments, and so forth.
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Online StoreMolecular Biology Universal Kit
A selection of 12 x 25ml molecular biology relevant buffers. These buffers are routinely used in molecular biology and are all DNase and RNase free. The buffers supplied are listed on the product details page of the online store.
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LongLife™ Enzyme Preparations
Enzymes regularly used in laboratory applications often require preparation of fresh solution before each use. Making fresh enzyme solution for each application is time consuming and wasteful. A wide variety of enzyme preparations in a ready-to-use format are offered. Online Store

LongLife™ enzyme preparations have a long shelf life and no weighing or buffer preparation is needed; simply take an aliquot and add in your sample. LongLife™ enzyme preparations contain cofactors necessary for optimal enzymatic activity. Supplied in suspension form and when stored properly have a one year shelf life.
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Proteinase K
Proteinase K (also protease K, endopeptidase K, peptidase K or Tritirachium alkaline phosphatase) (EC 3.4.21.64) is a nonspecific, broad spectrum serine protease that is isolated from the saprophytic fungus Tritirachium album.

Online StoreProteinase K is routinely used for the purification of target material from contaminating proteins, for the isolation of RNA and DNA and to inactivate other protein enzymatic activities. Proteinase K exhibits high activity in the presence of SDS, urea and EDTA. This allows the use of EDTA in the purification of DNA or RNA to inhibit calcium dependent nucleases.
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