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dsDNase Enzyme

Original price was: $1,195.00.Current price is: $595.00.

Catalog Number: B2016874 (5U)
dsDNase Enzyme is a high quality efficient enzyme used for the specific removal of double-stranded DNA (dsDNA) from RNA samples. It is commonly used in molecular biology and biochemistry research to eliminate contaminating DNA that may interfere with downstream applications such as reverse transcription or PCR. dsDNase is designed to be fast-acting and easy to use, making it a valuable tool for researchers working with RNA samples. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

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Product Description

dsDNase Enzyme
Catalog number: B2016874
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 5U
Molecular Weight or Concentration: N/A
Supplied as: Solution
Applications: a molecular tool for various biochemical applications
Storage: -20°C
Keywords: dsDNase
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Liu W, Yue S, Zheng X, Hu M, Cao J, Zheng Y. aFARP-ChIP-seq, a convenient and reliable method for genome profiling in as few as 100 cells with a capability for multiplexing ChIP-seq Epigenetics. 2019 Sep;14(9):877-893.
2: Lee J, Kim JH, Kang SH, Yoo HM. Improvement of digital PCR conditions for direct detection of KRAS mutations J Clin Lab Anal. 2020 Aug;34(8):e23344.
3: Zhou C, Zhao Y, Guo B, Yang M, Xu Q, Lei C, Wang H. Establishment of a Simple, Sensitive, and Specific Salmonella Detection Method Based on Recombinase-Aided Amplification Combined with dsDNA-Specific Nucleases Foods. 2024 Apr 29;13(9):1380.
4: Kumar GNM, Kannangara CG, Knowles NR. Nucleases are upregulated in potato tubers afflicted with zebra chip disease Planta. 2022 Feb 1;255(3):54.
5: Lee J, Kim JH, Kang SH, Yoo HM. Improvement of digital PCR conditions for direct detection of KRAS mutations J Clin Lab Anal. 2020 Aug;34(8):e23344.
6: Robertson NM, Toscano AE, LaMantia VE, Hizir MS, Rana M, Balcioglu M, Sheng J, Yigit MV. Unlocked Nucleic Acids for miRNA detection using two dimensional nano-graphene oxide Biosens Bioelectron. 2017 Mar 15;89(Pt 1):551-557.
7: Stinson LF, Keelan JA, Payne MS. Identification and removal of contaminating microbial DNA from PCR reagents: impact on low-biomass microbiome analyses Lett Appl Microbiol. 2019 Jan;68(1):2-8.
8: Huang HJ, Cui JR, Xia X, Chen J, Ye YX, Zhang CX, Hong XY. Salivary DNase II from Laodelphax striatellus acts as an effector that suppresses plant defence New Phytol. 2019 Oct;224(2):860-874.
9: Jámbrik K, Máthé C, Vasas G, Beyer D, Molnár E, Borbély G, M-Hamvas M. Microcystin-LR induces chromatin alterations and modulates neutral single-strand-preferring nuclease activity in Phragmites australis J Plant Physiol. 2011 May 1;168(7):678-86.
10: Liu W, Yue S, Zheng X, Hu M, Cao J, Zheng Y. aFARP-ChIP-seq, a convenient and reliable method for genome profiling in as few as 100 cells with a capability for multiplexing ChIP-seq Epigenetics. 2019 Sep;14(9):877-893.

Products Related to dsDNase Enzyme can be found at Enzymes

Additional Information

Weight 48 oz
Dimensions 8 × 8 × 8 in

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