Category: Molecular Biology Reagents

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  • Categories: Enzymes
  • Categories: Food and Water assays
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Reference: 32-1010

Kit for the extraction of microbial DNA from water samples. For filtration units with 47 or 50 mm frits includes filtration membranes.

Reference: AC115

Proteinase K is a non-specific serine protease. This enzyme exhibits high stability and activity in the presence of SDS, EDTA, and urea, as well as over a wide pH range. Proteinase K is useful for the inactivation of nucleases and lysis during the isolation of DNA and RNA.

Reference: ISWAB‐DNA‐1200

DNA collection kit for humans that can capture samples producing high yields of double stranded, long fragmented DNA from buccal cells using traditional swabs.

Reference: 32-1050

Kit for the extraction of microbial DNA from water samples. For filtration units with 47 or 50 mm frits includes filtration membranes.

Reference: AC116

Proteinase K is a non-specific serine protease. This enzyme exhibits high stability and activity in the presence of SDS, EDTA, and urea, as well as over a wide pH range. Proteinase K is useful for the inactivation of nucleases and lysis during the isolation of DNA and RNA.

Reference: ISWAB‐DNA‐250

DNA collection kit for humans that can capture samples producing high yields of double stranded, long fragmented DNA from buccal cells using traditional swabs.

Reference: ev-8

1.25 µg pSpot8 vector, S.cerevisiae, Spot C-term, Leu/Amp (Ori: 2µ/pBR322), high expression.

Reference: AC117

For RNase digestion during DNA preparation. RNase A is endonuclease-free and has been rigorously tested for RNA digestion activity in plasmid purification procedures.

Reference: ISWAB‐RNA‐v2

The iSWAB-RNA-v2 device allows for the non-invasive collection, concentration, and stabilization of intact buccal cells and/or any mammalian cells collected with a swab or cytobrush allowing for real time ambient stabilization of total RNA from the point of collection to processing. Maintaining RNA stability and protecting it from degradation is a significant challenge, while current RNA stabilization methods such as PAXgene, Tempus, RNAgard or dry blood spots require invasive blood collection resulting in low compliance.