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NEBuffer 4
MfeI-HF
New | High-Fidelity Enzymes
Cloned At NEBRecombinant SourceEngineered EnzymeTime SaverStar Activity ReducedNEBuffer 437Heat InactivatedPass Blue White Selection Assay
Catalog # Size Concentration Price Qty  
R3589S 500 units 20,000 units/ml $66.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Recognition Site:

CAATTG

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

FAQs


  1. What does HF refer to following the name of the restriction enzyme?
  2. When should I choose the HF version of the enzyme?
  3. When is star activity a concern?
  4. Why does the HF version of the enzyme have a different recommended buffer than the wild type enzyme?
  5. Can the change in buffer preference of the HF enzyme be advantageous?
  6. Will the HF enzyme produce elevated star activity when used in a buffer other than the one recommended?
  7. What does it mean to be Time-Saver qualified?
  8. How is the improvement in fidelity of HF restriction endonucleases quantitated?
  9. What is the Fidelity Index (FI)?
  10. How does the level of star activity of MfeI-HF compare to MfeI?
  11. What is the difference between MfeI-HF and MfeI?
  12. What is the specific activity of MfeI-HF?
  13. Is there any difference in the methylation sensitivity between MfeI-HF and MfeI?
  14. 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

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