The kit contains HL-dsDNase which efficiently removes gDNA from RNA preps before running RT-qPCR.
gDNA is removed, leaving RNA ready for reverse transcription in the same tube.
Heat-labile dsDNase can easily be inactivated.
This procedure minimizes pipetting steps and reduces hands-on time.
The Heat&Run kit is especially well suited for high throughput experiments.
The high activity of the HL-dsDNase at low temperature and its heat-lability makes it ideal to use in a combination with a heat activated RT enzyme. The contaminating genomic DNA is cleaved at ambient temperature and increasing the temperature over 50°C will inactivate the DNase and start the Reverse Transcriptase.
Kit Contents
10X reaction Buffer
HL-dsDNase (50 reactions)
Storage Conditions: Store at -20˚C. Sample Material: The Heat&Run kit is suited for gDNA removal of RNA from any source. Quality Control: The kit is tested for absence of RNase.
Emerging recombinant noroviruses identified by clinical and waste water screening Jennifer H. Lun, Joanne Hewitt, Alefiya Sitabkhan, John-Sebastian Eden, Daniel Enosi Tuipulotu, Natalie E. Netzler, Leigh Morrell, Juan Merif, Richard Jones, Bixing Huang, David Warrilow, Kelly-Anne Ressler, Mark J. Ferson, Dominic E. Dwyer, Jen Kok, William D. Rawlinson, Daniel Deere, Nicholas D. Crosbie & Peter A. White (2018) Emerging Microbes & Infectionsvolume 7, Article number: 50 (2018)
Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutationAnnelot Baert, Julie Depuydt, Tom Van Maerken, Bruce Poppe, Fransiska Malfait, Katrien Storm, Jenneke van den Ende, Tim Van Damme, Sylvia De Nobele, Gianpaolo Perletti, Kim De Leeneer, Kathleen B. M. Claes, and Anne Vral (2016) Breast Cancer Research : BCR 18 (2016): 52. PMC. Web. 1 June 2016.
The kit contains HL-dsDNase which efficiently removes gDNA from RNA preps before running RT-qPCR.
gDNA is removed, leaving RNA ready for reverse transcription in the same tube.
Heat-labile dsDNase can easily be inactivated.
This procedure minimizes pipetting steps and reduces hands-on time.
The Heat&Run kit is especially well suited for high throughput experiments.
The high activity of the HL-dsDNase at low temperature and its heat-lability makes it ideal to use in a combination with a heat activated RT enzyme. The contaminating genomic DNA is cleaved at ambient temperature and increasing the temperature over 50°C will inactivate the DNase and start the Reverse Transcriptase.
Kit Contents
10X reaction Buffer
HL-dsDNase (50 reactions)
Storage Conditions: Store at -20˚C. Sample Material: The Heat&Run kit is suited for gDNA removal of RNA from any source. Quality Control: The kit is tested for absence of RNase.
Emerging recombinant noroviruses identified by clinical and waste water screening Jennifer H. Lun, Joanne Hewitt, Alefiya Sitabkhan, John-Sebastian Eden, Daniel Enosi Tuipulotu, Natalie E. Netzler, Leigh Morrell, Juan Merif, Richard Jones, Bixing Huang, David Warrilow, Kelly-Anne Ressler, Mark J. Ferson, Dominic E. Dwyer, Jen Kok, William D. Rawlinson, Daniel Deere, Nicholas D. Crosbie & Peter A. White (2018) Emerging Microbes & Infectionsvolume 7, Article number: 50 (2018)
Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutationAnnelot Baert, Julie Depuydt, Tom Van Maerken, Bruce Poppe, Fransiska Malfait, Katrien Storm, Jenneke van den Ende, Tim Van Damme, Sylvia De Nobele, Gianpaolo Perletti, Kim De Leeneer, Kathleen B. M. Claes, and Anne Vral (2016) Breast Cancer Research : BCR 18 (2016): 52. PMC. Web. 1 June 2016.