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NEBuffer 4
Hpy166II
Cloned At NEBRecombinant SourceTime SaverNEBuffer 437Heat Inactivated
Catalog # Size Concentration Price Qty  
R0616L 2,500 units 10,000 units/ml $252.00
R0616S 500 units 10,000 units/ml $63.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Recognition Site:

GTNNAC

isoschizomers | compatible ends | single letter code

Source:
A E. coli strain that carries the cloned Hpy166II gene from Helicobacter pylori J166 (M.J. Blaser)

Reagents Supplied:
NEBuffer 4


Enzyme Properties


Activity in NEBuffers:
NEBuffer 1:100%
NEBuffer 2:100%
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: Not sensitive
CpG methylation: Blocked

Heat Inactivation:
65°C for 20 minutes

Survival in a Reaction:
Minimum units to digest 1 µg of substrate DNA in 16 hours: 0.13 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 pBR322 in 1 hour at 37°C in total reaction volume of 50  μl.

Concentration:
10,000 units/ml

Unit Assay Substrate:
pBR322 DNA

Storage Conditions:
10 mM Tris-HCl
50 mM KCl
1 mM Dithiothreitol
0.1 mM EDTA
200 µg/ml BSA
50% Glycerol
pH 7.4 @ 37°C

Storage Temperature:
-20°C

Diluent Compatibility:
Diluent A


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 Hpy166II, > 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 Hpy166II.


16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA and 200 units of Hpy166II 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 Hpy166II 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

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