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NEBuffer 3
Nt.BspQI
Cloned At NEBRecombinant SourceTime SaverNEBuffer 350Heat Inactivated
Catalog # Size Concentration Price Qty  
R0644L 5,000 units 10,000 units/ml $252.00
R0644S 1,000 units 10,000 units/ml $63.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Recognition Site:

GCTCTTC

isoschizomers | single letter code

Description:
Nt.BspQI is a nicking endonuclease that cleaves only one strand of DNA on a double-stranded DNA substrate.

Source:
An E. coli strain expressing an engineered BspQI variant from BspQI restriction enzyme

Reagents Supplied:
NEBuffer 3 (10X)


Enzyme Properties


Activity in NEBuffers:
NEBuffer 1:10%
NEBuffer 2:75%
NEBuffer 3:100%
NEBuffer 4:25%

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

Activity at 37°C:
80%

Heat Inactivation:
80°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 3
Incubate at 50°C.

1X NEBuffer 3:
50 mM Tris-HCl
100 mM NaCl
10 mM MgCl2
1 mM Dithiothreitol
pH 7.9 @ 25°C

Unit Definition:
One unit is defined as the amount of enzyme required to convert 1 μg of supercoiled pUC19 DNA to open circular form in 1 hour at 50°C in a total reaction volume of 50 μl.

Concentration:
10,000 units/ml

Unit Assay Substrate:
pUC19 DNA

Storage Conditions:
10 mM Tris-HCl
300 mM NaCl
1 mM Dithiothreitol
0.1 mM EDTA
500 µg/ml BSA
50% Glycerol
pH 7.4 @ 25°C

Storage Temperature:
-20°C

Diluent Compatibility:
Diluent B


Notes


General notes:
  1. Incubation at 37°C results in 80% activity.

Quality Control for Current Lot


Quality control values for a specific lot can be found on the datacard which accompanies each product.

16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA and 100 units of Nt.BspQI incubated for 16 hours at 50ºC 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 Nt.BspQI with 1 μg of a mixture of single and double-stranded [3H] E. coli DNA (205 cpm/μg) for 4 hours at 50ºC released < 0.1% of the total radioactivity.


Reagents Sold Separately


NEBuffer 3

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