 |
|
 |
 |
 |
| Home >
Products >
Restriction Endonucleases >
Restriction Endonucleases >
MfeI-HF™ |  |  |  | | MfeI-HF™ |  |  | New | High-Fidelity Enzymes |  |
|  |
 |
|
Prices are in US dollars and valid only for US orders.
|

 Recognition Site:


 isoschizomers | compatible ends | single letter code
Source: An E. coli strain that carries the cloned and modified (Q13A/F35Y) MfeI gene from Mycoplasma fermentas (N.F. Halden)
Reagents Supplied: NEBuffer 4 (10X)
Enzyme Properties

 Activity in NEBuffers:
| NEBuffer 1: |  | 75% | | NEBuffer 2: |  | 50% | | NEBuffer 3: |  | 10% | | 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: Not sensitive | | CpG methylation: Not sensitive |
Heat Inactivation: 65°C for 10 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 4 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 λ DNA in 1 hour at 37°C in a total reaction volume of 50 µl.
Concentration: 20,000 units/ml
Unit Assay Substrate: λ DNA
Storage Conditions: 10 mM Tris-HCl 50 mM NaCl 1 mM DTT 0.1 mM EDTA 200 µg/ml BSA 50% Glycerol
pH 7.4 @ 25°C
Storage Temperature: -20°C
Diluent Compatibility: Diluent A
Notes

 Usage notes:- MfeI-HF™ has the same specificity as MfeI (NEB #R0589), but it has been engineered for reduced star activity.
FAQs


- What does HF refer to following the name of the restriction enzyme?
- When should I choose the HF version of the enzyme?
- When is star activity a concern?
- Why does the HF version of the enzyme have a different recommended buffer than the wild type enzyme?
- Can the change in buffer preference of the HF enzyme be advantageous?
- Will the HF enzyme produce elevated star activity when used in a buffer other than the one recommended?
- What does it mean to be Time-Saver qualified?
- How is the improvement in fidelity of HF restriction endonucleases quantitated?
- What is the Fidelity Index (FI)?
- How does the level of star activity of MfeI-HF compare to MfeI?
- What is the difference between MfeI-HF and MfeI?
- What is the specific activity of MfeI-HF?
- Is there any difference in the methylation sensitivity between MfeI-HF and MfeI?
- Is there a difference in cutting close to the ends between MfeI-HF and MfeI?
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 20-fold overdigestion with MfeI-HF™, > 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 MfeI-HF™.
16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA
and 35 units of MfeI-HF™ 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 100 units of MfeI-HF™ with 1 μg of a mixture of single and double-stranded
[3H] E. coli DNA (205 cpm/μg) for 4 hours at 37ºC
released < 0.3% of the total radioactivity.
Endonuclease Activity:
Incubation of a 50 μl reaction containing 70 units of MfeI-HF™ with 1 μg of
pUC19 DNA for 4 hours at 37ºC resulted
in < 5% conversion to RFII as determined by agarose gel electrophoresis.
Blue/White Screening Assay:
An appropriate vector is digested at a unique site within the
lacZα gene with a 10-fold excess of enzyme.
The vector DNA is then ligated, transformed, and plated onto Xgal/IPTG/Amp plates.
Successful expression of β-galactosidase is a function of how intact its gene remains after cloning,
an intact gene gives rise to a blue colony, removal of even a single base gives rise to a white colony.
Enzyme preparations must produce fewer than 3% white colonies to be Blue/White certified.
Reagents Sold Separately

 NEBuffer 4
Legal

 Patents: The National Institute of Health: Licensed Under U.S. Patent No. 4,935,367 The United States of America as represented by the Department of Health: Licensed Under U.S. Patent No. 5,073,486
| |
 |
 |
|
 |