Volcano3G® RT-PCR 2x Master Mix (+GreenDye)

Catalog Number: #6301

Write Your Own Review
You're reviewing:Volcano3G® RT-PCR 2x Master Mix (+GreenDye)
Your Rating
Key Features

(q)PCR, RT-(q)PCR

Qty:
+ -
Qty:
+ -

Custom Quote

Product Overview
Product NameVolcano3G® RT-PCR 2x Master Mix (+GreenDye)
Catalog Number#6301
Description

Volcano3G® RT-PCR 2x Master Mix (+GreenDye) is a ready-to-use master mix for reliable qPCR and RT-qPCR in all standard PCR cyclers. The mix contains an aptamer-based fast-start formulated enzyme blend of a robust Taq DNA polymerase and an engineered thermostable Volcano3G® DNA polymerase with reverse transcriptase activity. The mix is supplemented with a highly sensitive GreenDye (#2000) with low polymerase inhibition. Volcano3G® RT-PCR master mix enables amplification of RNA target sequences with quick and easy PCR protocols, even including "zero-step" amplification.

For more information, please check :
Volcano3G® RT-PCR 2x Master Mix (+GreenDye)

Application(q)PCR, RT-(q)PCR
BrandmyPOLS Biotec
Further Specification
Content

S pack: 1 x 1.25 ml Volcano3G® RT-PCR 2x Master Mix (+GreenDye)

M pack: 5 x 1.25 ml Volcano3G® RT-PCR 2x Master Mix (+GreenDye)

Storage and Shipping
Storage -20°C
ShippingCold packs
References
References

Zander, J., Scholtes, S., Ottinger, M., Kremer, M., Kharazi, A., Stadler, V., ... & Hauck, C. R. (2021). Self-Collected Gargle Lavage Allows Reliable Detection of SARS-CoV-2 in an Outpatient Setting. Microbiology spectrum, 9(1), e00361-21.

Kuiper, J. W., Baade, T., Kremer, M., Kranaster, R., Irmisch, L., Schuchmann, M., ... & Hauck, C. R. (2020). Detection of SARS-CoV-2 from raw patient samples by coupled high temperature reverse transcription and amplification. PloS one, 15(11), e0241740.

Schwaderer, J., Phan, T. S., Glöckner, A., Delp, J., Leist, M., Brunner, T., & Delgado, M. E. (2020). Pharmacological LRH-1/Nr5a2 inhibition limits pro-inflammatory cytokine production in macrophages and associated experimental hepatitis. Cell death & disease, 11(2), 1-13.

Chovancova, P., Merk, V., Marx, A., Leist, M., & Kranaster, R. (2017). Reverse-transcription quantitative PCR directly from cells without RNA extraction and without isothermal reverse-transcription: a ‘zero-step’RT-qPCR protocol. Biology Methods and Protocols, 2(1), bpx008.

Reviews