Heat&Run gDNA Removal Kit

Heat&Run gDNA Removal Kit

Brand: ArcticZymes
In stock
SKU
Heat&Run gDNA Removal Kit

Kit allows rapid, effortless and complete removal of gDNA in RNA preps from any source

Grouped product items
Product Name Size
Heat&Run gDNA Removal Kit
SKU: 80200-50
50 Rxns
Heat&Run gDNA Removal Kit
SKU: 80200-250
250 Rxns
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Heat&Run gDNA Removal Kit
Heat&Run gDNA Removal Kit

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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.

  1. Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice
    Marjolijn Renard, Suzanne Vanhauwaert, Marine Vanhomwegen, Ali Rihani, Niels Vandamme, Steven Goossens, Geert Berx, Pieter Van Vlierberghe, Jody J. Haigh, Bieke Decaesteker, Jolien Van Laere, Irina Lambertz, Frank Speleman, Jo Vandesompele & Andy Willaert (2018)
    Scientific Reports vol 8, Article number: 7642 (2018)
  2. Transcriptome Profiling Reveals Interplay of Multifaceted Stress Response in Escherichia coli on Exposure to Glutathione and Ciprofloxacin
    Manish Goswami, Akkipeddi Venkat Satya Surya Narayana Rao (2018)
    American Society for Microbiology Journals, February 13, 2018.
  3. 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)
  4. Complete Coding Sequence of a Case of Chikungunya Virus Imported into Australia
    Bixing Huang, Alyssa T. Pyke, Jamie McMahon, David Warrilow (2017)
    Genome Announc. May 2017 vol. 5 no. 19 e00310-17
  5. 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.
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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.

  1. Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice
    Marjolijn Renard, Suzanne Vanhauwaert, Marine Vanhomwegen, Ali Rihani, Niels Vandamme, Steven Goossens, Geert Berx, Pieter Van Vlierberghe, Jody J. Haigh, Bieke Decaesteker, Jolien Van Laere, Irina Lambertz, Frank Speleman, Jo Vandesompele & Andy Willaert (2018)
    Scientific Reports vol 8, Article number: 7642 (2018)
  2. Transcriptome Profiling Reveals Interplay of Multifaceted Stress Response in Escherichia coli on Exposure to Glutathione and Ciprofloxacin
    Manish Goswami, Akkipeddi Venkat Satya Surya Narayana Rao (2018)
    American Society for Microbiology Journals, February 13, 2018.
  3. 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)
  4. Complete Coding Sequence of a Case of Chikungunya Virus Imported into Australia
    Bixing Huang, Alyssa T. Pyke, Jamie McMahon, David Warrilow (2017)
    Genome Announc. May 2017 vol. 5 no. 19 e00310-17
  5. 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.
Write Your Own Review
You're reviewing:Heat&Run gDNA Removal Kit
Your Rating