Category: Molecular Biology Reagents

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  • Categories: DNA polymerases
  • Categories: Enzymes
  • Categories: Sample collection
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: PCE0101

highQu ALLin™ Taq DNA Polymerase is the versatile engineered enzyme which in combination with the optimized ALLin™ buffer provides higher success rates in demanding PCR applications like amplification of complex templates, crude sample PCR and fast cycling. ALLin™ Taq DNA Polymerase has the same PCR accuracy like Taq DNA Polymerase, 4.5 x 10^4 (a number of correct nucleotides incorporated before the first error). ALLin™ Taq DNA Polymerase produces A-tailed products suitable for ligating into TA cloning vectors. For the maximum convenience the ALLin™ Taq Mastermix, 2X is available. 

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: PCE0105

highQu ALLin™ Taq DNA Polymerase is the versatile engineered enzyme which in combination with the optimized ALLin™ buffer provides higher success rates in demanding PCR applications like amplification of complex templates, crude sample PCR and fast cycling. ALLin™ Taq DNA Polymerase has the same PCR accuracy like Taq DNA Polymerase, 4.5 x 10^4 (a number of correct nucleotides incorporated before the first error). ALLin™ Taq DNA Polymerase produces A-tailed products suitable for ligating into TA cloning vectors. For the maximum convenience the ALLin™ Taq Mastermix, 2X is available. 

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. 

Reference: PCM0201

highQu ALLin™ Taq DNA Polymerase is the versatile engineered enzyme which in combination with the optimized ALLin™ buffer provides higher success rates in demanding PCR applications like amplification of complex templates, crude sample PCR and fast cycling. ALLin™ Taq DNA Polymerase has the same PCR accuracy like Taq DNA Polymerase, 4.5 x 10^4 (a number of correct nucleotides incorporated before the error occurs) and produces A-tailed products suitable for ligating into TA cloning vectors. The convenience of ALLin™ Taq DNA Polymerase is maximized by the use of 2X Red Mastermix providing the additional advantage of reduced pipetting and minimized errors. ALLin™ Red Taq Mastermix, 2X is premixed with red dye and density reagents for direct loading on the gels after the PCR. In a 2% agarose TAE gel the dye migrates with~350 bp DNA, in 1% agarose TAE gel with ~ 600 bp DNA fragments. The mastermix is even supplied with the PCR Water, and the only thing to add is the template with primers.

Reference: AC118

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‐P‐1200

Non-invasive sample collection tube for collection and stabilization of protein and DNA in the same oral sample.  Oral sample collection has gained widespread acceptance due to its non-invasive nature and because continuous visual contact of the collection process is possible.  Current non-invasive collection products are designed for immediate detection using stick-based technology, but are limited to simple yes/no answers.  If additional data is required, a more robust collection method coupled with high-sensitivity downstream analysis is necessary.

Reference: PCM0205

highQu ALLin™ Taq DNA Polymerase is the versatile engineered enzyme which in combination with the optimized ALLin™ buffer provides higher success rates in demanding PCR applications like amplification of complex templates, crude sample PCR and fast cycling. ALLin™ Taq DNA Polymerase has the same PCR accuracy like Taq DNA Polymerase, 4.5 x 10^4 (a number of correct nucleotides incorporated before the error occurs) and produces A-tailed products suitable for ligating into TA cloning vectors. The convenience of ALLin™ Taq DNA Polymerase is maximized by the use of 2X Red Mastermix providing the additional advantage of reduced pipetting and minimized errors. ALLin™ Red Taq Mastermix, 2X is premixed with red dye and density reagents for direct loading on the gels after the PCR. In a 2% agarose TAE gel the dye migrates with~350 bp DNA, in 1% agarose TAE gel with ~ 600 bp DNA fragments. The mastermix is even supplied with the PCR Water, and the only thing to add is the template with primers.