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YEASEN

[YEASEN] Recombinant Deoxyribonuclease I (DNase I,RNase-free) GMP-grade (2 U/μL)

Cat-No. 10611ES
10611ES76 - 500U
10611ES92 - 10000U

YEASEN은 생명과학 연구 및 진단을 위한 고품질의 연구용 시약과 기기를 제공하는 글로벌 바이오 기업입니다.




제품 설명


Recombinant Deoxyribonuclease I  (DNase I,RNase-free) GMP-grade (2 U/μL)




제품 번호


10611ES76 - 500U

10611ES92 - 10000U




제품 설명


Description

DNase I is an endonuclease that can digest single-stranded and double-stranded DNA to produce single deoxynucleotides or single-stranded or double-stranded oligodeoxynucleotides. It can hydrolyze the phosphodiester bond to produce monodeoxynucleotides and oligodeoxynucleotides containing 5'-phosphate groups and 3'-OH groups. The average digestion product is the smallest polytetranucleotide. DNase I can catalyze many forms of DNA, such as single-stranded DNA, double-stranded DNA, and even chromatin (its cutting rate is affected by histones). The optimum pH range is 7-8. The activity of DNase I depends on Ca2+ and can be activated by divalent metal ions, such as Co2+, Mn2+, Zn2+, etc. 5 mM Ca2+ can protect the enzyme from being hydrolyzed. In the presence of Mg2+, the enzyme can recognize and cut any site on any strand of DNA randomly; and in the presence of Mn2+, it can recognize two strands of DNA at the same time and cut at almost the same site to form blunt ends, Or sticky ends with 1-2 nucleotides protruding. DNase I is widely used in the preparation of DNA-free RNA; remove the template DNA after in vitro transcription; prepare DNA-free RNA before RT-PCR and RT-qPCR reactions; combine with DNA polymerase I to perform DNA labeling through nick translocation; DNA fragmentation library construction.
This product is produced in accordance with GMP process requirements, and the product is provided in liquid form.

Feature

  • DNA specific Endonuclease
  • Degrades double-stranded and single-stranded DNA
  • Products are short oligos with 5'-phosphate and 3'-OH

Application

  • Removal of contaminating genomic DNA from RNA samples
  • Degradation of DNA templates in transcription reactions


Specification

SourceRecombinant E. coli with DNase I gene
Optimum temperature37℃
Storage Buffer10 mM Tris-HCl pH 7.6,2 mM CaCl2, 50% (v/v) Glycerol 
Unit DefinitionThe amount of enzyme required to completely degrade 1 μg of plasmid DNA within 10 min at 37°C. (The reaction buffer is: 10 mM Tris-HCl pH 7.6, 2.5 mM MgCl2, 0.5 mM CaCl2, 1 μg plasmid DNA)


Components

Components No.Name10611ES76 (500 U)10611ES84 (2,000 U)10611ES92 (10,000 U)
10611Deoxyribonuclease I (DNase I) GMP-grade (2 U/μL)250 μL1 mL5 mL


Shipping and Storage

Deoxyribonuclease I (DNase I) GMP-grade products are shipped with dry ice and can be stored at -15℃ ~ -25℃ for one year.


Figures

Figure 1. DNase I from YEASEN could effectively remove DNA template during transcription,compared with competitor brands.


Citations & References:

[1] Lu Z, Liu H, Song N, et al. METTL14 aggravates podocyte injury and glomerulopathy progression through N<sup>6</sup>-methyladenosine-dependent downregulating of Sirt1. Cell Death Dis. 2021;12(10):881. Published 2021 Sep 27. doi:10.1038/s41419-021-04156-y(IF:8.469)

[2] Yu Y, Wang Y, Zhang W, et al. Biomimetic periosteum-bone substitute composed of preosteoblast-derived matrix and hydrogel for large segmental bone defect repair. Acta Biomater. 2020;113:317-327. doi:10.1016/j.actbio.2020.06.030(IF:7.242)




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