Bsp143I (Sau3AI)
5'-^G A T C -3' 3'- C T A G^-5'
digested lambda DNA
1.4% agarose![]()
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#ER0781
Supplied with:
10X Buffer Bsp143I
10X Buffer Tango™300 u
1 ml
1 ml#ER0782
Supplied with:
10X Buffer Bsp143I
10X Buffer Tango™1500 u
1 ml
1 mlCommercial Isoschizomers:
BfuCI, BssMI, (BstKTIm), BstMBI, (DpnI), DpnIIm, Kzo9I,
(MalI), MboIm, NdeIIm, Sau3AIm
Enzymes in parentheses have different cleavage specificities.
"m" indicates different sensitivity to methylation.Related Documents (in pdf, ~55 KB):
Certificate of Analysis: #ER0781, #ER0782
MSDS (English)
MSDS (English-USA)
MSDS (German)
Chart (in pdf, 721 KB)
Brochure (in pdf, 316 KB)Concentration
10 u/µlConditions for 100% Activity
Recommended
bufferIncubation
temperatureUnits for
overnight
incubation,
u/µg DNAThermal
inactivation,
in 20 minEnzyme activity, %
Bsp143I
(unique)B
(blue)G
(green)O
(orange)R
(red)Tango™
(yellow)1X 1X 1X 1X 1X 1X 2X Buffer Bsp143I 37°C 0.1 65°C 100 20-50 20-50 0-20 0-20 50-100 20-50 Storage Buffer
10 mM Tris-HCl (pH 7.5 at 25°C), 50 mM KCl, 1 mM DTT, 0.1 mM EDTA, 0.15% Triton X-100, 0.2 mg/ml BSA and 50% glycerol.Ligation and Recleavage
After 50-fold overdigestion with Bsp143I, more than 95% of the digested DNA fragments can be ligated and recut.
Methylation Effects Dam:
Dcm:
CpG:
EcoKI:
EcoBI:completely overlaps
never overlaps
may overlap
never overlaps
may overlap- no effect.
- no effect.
- blocked.
- no effect.
- no effect.Double Digestions using Tango™ Buffer, DoubleDigest™
Optimal
bufferEnzyme activity, %
Tango™
(yellow)1X 2X Buffer Bsp143I 50-100 20-50 Number of Recognition Sites in DNA Molecules
Lambda PhiX174 M13mp18/19 pBR322 pUC18/19 pUC57 pTZ19R/U pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184 116 0 7 22 15 15 15 15 15 22 15
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See also General Properties of Restriction Enzymes:
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Updated kovo 05, 2008 16:41