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Cat. No. |
CMC04 |
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Product
Overview |
DNase I is a
glycosylated polypeptide that is commonly used to degrade
unwanted single- and double-stranded DNA into
5´phosphodinucleotide and oligonucleotide fragments. The
properties of DNase I can be modified by divalent ions. For
example, in the presence of Mg2+, Ca2+ or Zn2+, DNase I degrades
DNA by making random single-strand nicks in the phosphate
backbone. In the presence of divalent transition metals such as
Mn2+ or Co2+, DNase I creates double-strand breaks, resulting in
fragments with 0-2 nucleotide overhangs. DNase I is suitable for
removal of genomic DNA from cell lysates, removal of plasmid
from in vitro transcribed RNA, nick translation and DNase I
footprinting. |
|
Source |
E.coli |
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Packaging |
DNase I(RNase
Free)(5U/ul)
1000U, 200ul, 2×DNase
Buffer, 1000ul. |
|
Concentration |
5U/ul |
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Unit
Definition |
One unit is
that amount of enzyme causing an increase in absorbance at 260
nm by 0.001 per minute at 25°C. |
|
Reaction buffer |
[2×DNase
Buffer ] 200mM Tris-HCl (pH7.5, 20mM CaCl2, 20mM MgCl2. |
|
Storage buffer |
[pH5.3]75mM
NaCl, 10mM NaAc, 50% glycerol(v/v) |
|
Application |
RT-PCR; In
vitro transcription; Nick translation; Shot gun sequencing; Foot
printing. |
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Storage |
-20°C. |
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