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NEBuffer 3
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dam-/dcm- Competent E. coli
BsaI
Cloned At NEBRecombinant SourceNEBuffer 350Heat InactivatedDCM
Catalog # Size Concentration Price Qty  
R0535L 5,000 units 10,000 units/ml $244.00
R0535S 1,000 units 10,000 units/ml $61.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Recognition Site:

GGTCTC

isoschizomers | compatible ends | single letter code

Source:
A E. coli strain that carries the BsaI gene from Bacillus stearothermophilus 6-55 (Z. Chen).

Reagents Supplied:
NEBuffer 3 (10X)


Enzyme Properties


Activity in NEBuffers:
NEBuffer 1:75%
NEBuffer 2:75%
NEBuffer 3:100%
NEBuffer 4:50%

When using a buffer other than the optimal (supplied) NEBuffer, it may be necessary to add more enzyme to achieve complete digestion.

Methylation Sensitivity:
dam methylation: Not sensitive
dcm methylation: Blocked by overlapping
CpG methylation: Blocked by some combinations of overlapping

Activity at 37°C:
10%

Heat Inactivation:
65°C for 20 minutes

Survival in a Reaction:
Minimum units to digest 1 µg of substrate DNA in 16 hours: 1.00 unit(s)


Reaction & Storage Conditions


Reaction Conditions:
1X NEBuffer 3
Incubate at 50°C.

1X NEBuffer 3:
50 mM Tris-HCl
100 mM NaCl
10 mM MgCl2
1 mM Dithiothreitol
pH 7.9 @ 25°C

Unit Definition:
One unit is defined as the amount of enzyme required to digest 1 µg of T7 DNA in 1 hour at 50°C in a total reaction volume of 50 µl.

Concentration:
10,000 units/ml

Unit Assay Substrate:
T7 DNA

Storage Conditions:
10 mM Tris-HCl
200 mM NaCl
1 mM Dithiothreitol
0.1 mM EDTA
200 µg/ml BSA
50% Glycerol
pH 7.4 @ 25°C

Storage Temperature:
-20°C

Diluent Compatibility:
Diluent B


Quality Control for Current Lot


Quality control values for a specific lot can be found on the datacard which accompanies each product.

Ligation and Re-cutting:
After a 10-fold overdigestion with BsaI, > 95% of the DNA fragments can be ligated with T4 DNA Ligase (at a 5' termini concentration of 1-2 μM) at 16ºC. Of these ligated fragments, > 95% can be recut with BsaI.


16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA and 200 units of BsaI incubated for 16 hours at 50ºC resulted in a DNA pattern free of detectable nuclease degradation as determined by agarose gel electrophoresis.

Exonuclease Activity:
Incubation of a 50 μl reaction containing 100 units of BsaI with 1 μg of a mixture of single and double-stranded [3H] E. coli DNA (205 cpm/μg) for 4 hours at 50ºC released < 0.05% of the total radioactivity.

Endonuclease Activity:
Incubation of a 50 μl reaction containing 50 units of BsaI with 1 μg of ΦX174 RF I DNA for 4 hours at 50ºC resulted in < 5% conversion to RFII as determined by agarose gel electrophoresis.


Reagents Sold Separately


NEBuffer 3


Companion Products


dam-/dcm- Competent E. coli


Legal


Patents:
New England Biolabs, Inc.: U.S. Patent No. 6,723,546

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