Recombinant DNase I Set (RNase-free, Yeast) _ 14550ES yeasen

$55.00
In stock
SKU
14550ES50
Catalog No.SizePrice (USD)
14550ES5050 T$55.00
14550ES72250 T$225.00

Product Description

DNase I, or Deoxyribonuclease I, is an endonuclease that can digest single-stranded or double-stranded DNA. It hydrolyzes phosphodiester bonds to produce monodeoxynucleotides and oligodeoxynucleotides containing 5'-phosphate groups and 3'-OH groups. The optimal working pH range of DNase I is 7-8. The activity of DNase I depends on Ca 2+ and can be activated by divalent metal ions such as Co 2+ , Mn 2+ , and Zn 2+ . In the presence of Mg 2+ , DNase I can randomly cut any site of double-stranded DNA; in the presence of Mn 2+ , DNase I can cut the DNA double strand at the same site, forming a blunt end or a sticky end with 1-2 nucleotides protruding, which can be used for the treatment of various RNA samples.

Features

  • Recombinant source, yeast
  • RNase-free
  • High enzymatic cleavage efficiency.
  • More suitable for applications sensitive to RNase.

Applications

  • Removal of contaminating genomic DNA from RNA samples
  • Degradation of DNA templates in transcription reactions
  • Removal of gDNA before RNA extraction or reverse transcription.
  • Removal of template DNA in in vitro transcription.

Specifications

  • Cat.N
  • o
  • Size
  • Price
  • 145
  • 50
  • ES
  • 5
  • 0
  • 50 T
  • 65
  • 145
  • 50
  • ES
  • 72
  • 250 T
  • 325

Components

  • Components No.
  • Name
  • 1
  • 4550
  • ES
  • 50
  • 1
  • 4550
  • ES
  • 7
  • 2
  • 1
  • 4550
  • A
  • Recombinant DNase I (RNase-free, Yeast)
  • 150 μL
  • 750 μL
  • 1
  • 4550
  • B
  • DNase I Reaction Buffer (10×)
  • 1 mL
  • 5×1 mL

Shipping and Storage

This product should be stored at -25~-15℃ for two year s

Figures

RNA extraction application verification

Figure 1 RNA extraction application verification 20 U of the enzyme preparation was used to treat 12 pre-treatment samples of mouse liver from different sources. RNA extraction and agarose gel electrophoresis analysis showed that the RNA integrity of the enzyme-treated group was good, indicating that this DNase I can effectively digest DNA without affecting the quality of RNA, and fully meets the technical requirements of RNA extraction experiments.

Safety Data Sheet

  • 1
  • 45
  • 50
  • _MSDS_HB
  • 250514
  • _EN.PDF

Manuals

  • 145
  • 50
  • _Manual_Ver.E
  • N
  • 20250514.pdf

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