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Restriction Endonucleases >
Restriction Endonucleases >
SexAI |
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 Recognition Site:


 isoschizomers | compatible ends | single letter code
Source: An E. coli strain that carries the SexAI gene from Streptomyces exfoliatus (B. Frey)
Reagents Supplied: NEBuffer 4 BSA
Enzyme Properties

 Activity in NEBuffers:
| NEBuffer 1: |  | 100% | | NEBuffer 2: |  | 75% | | NEBuffer 3: |  | 50% | | NEBuffer 4: |  | 100% |
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 | | CpG methylation: Not sensitive | |
More information about: Methylation Sensitivity |
Heat Inactivation: 65°C for 20 minutes
Survival in a Reaction: (+ +) Intermediate activity. Suitable for extended digestion, but < 8 hours. More information about: Extended Digests with Restriction Enzymes
Reaction & Storage Conditions

 Reaction Conditions: 1X NEBuffer 4 Supplemented with 100 μg/ml Bovine Serum Albumin Incubate at
37°C.
1X NEBuffer 4: 20 mM Tris-acetate 50 mM potassium acetate 10 mM Magnesium Acetate 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 pBC4 DNA (dcm-) in 1 hour at 37°C in a total reaction volume of 50 µl.
Concentration: 4,000 units/ml
Unit Assay Substrate: pBC4 DNA
Storage Conditions: 10 mM Tris-HCl 50 mM KCl 1 mM Dithiothreitol 0.1 mM EDTA 200 µg/ml BSA 50% Glycerol
pH 8.0 @ 25°C
Storage Temperature: -20°C
Diluent Compatibility: Diluent A
FAQs


- Do degenerate recognition sites need to be palindromic?
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 SexAI, approximately 75%
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, approximately 75% can be recut with SexAI.
16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA
and 16 units of SexAI 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 16 units of SexAI 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 4 BSA
Companion Products

 dam-/dcm- Competent E. coli
Legal

 Patents: New England Biolabs, Inc.: U.S. Patent No. 5,354,669
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England Biolabs, Inc. is an ISO 9001 and ISO
14001 Certified Company.
NEB certifies that it is a small business in accordance with the US Small Business Administration and 13 CFR 121.201 |
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