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Restriction Endonucleases >
Restriction Endonucleases >
SspI |
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 Recognition Site:


 isoschizomers | compatible ends | single letter code
Source: A E. coli strain that carries the SspI gene from Sphaerotilus species (ATCC 13925).
Reagents Supplied: NEBuffer SspI
Enzyme Properties

 Activity in NEBuffers:
| NEBuffer 1: |  | 50% | | NEBuffer 2: |  | 100% | | NEBuffer 3: |  | 50% | | 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: Not sensitive | | CpG methylation: Not sensitive |
Heat Inactivation: 65°C for 20 minutes
Survival in a Reaction: Minimum units to digest 1 µg of substrate DNA in 16 hours: 0.25 unit(s)
Reaction & Storage Conditions

 Reaction Conditions: 1X NEBuffer SspI Incubate at
37°C.
1X NEBuffer SspI: 100 mM Tris-HCl 50 mM NaCl 10 mM MgCl2 0.025 % Triton X-100
pH 7.5 @ 25°C
Unit Definition: One unit is defined as the amount of enzyme required to digest 1 µg of λ DNA in 1 hour at 37°C in a total reaction volume of 50 µl.
Concentration: 5,000 units/ml and 25,000 units/ml
Unit Assay Substrate: λ DNA
Storage Conditions: 10 mM Tris-HCl 200 mM NaCl 1 mM Dithiothreitol 0.1 mM EDTA 200 µg/ml BSA 50% Glycerol 0.15 mM Triton X-100
pH 7.4 @ 25°C
Storage Temperature: -20°C
Diluent Compatibility: Diluent C
Notes

 General notes:- Conditions of low ionic strength, high enzyme concentration, glycerol concentration > 5%, or pH > 8.0 may result in star activity.
FAQs


- What is Star Activity and how can it be avoided?
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 SspI, > 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 SspI.
16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA
and 30 units of SspI incubated for 16 hours at 37ºC
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 500 units of SspI with 1 μg of a mixture of single and double-stranded
[3H] E. coli DNA (205 cpm/μg) for 4 hours at 37ºC
released < 0.1% of the total radioactivity.
Reagents Sold Separately

 NEBuffer SspI
Companion Products

 SspI-HF™
Legal

 Patents: New England Biolabs, Inc.: U.S. Patent No. 5,516,678
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