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Reagents Sold Separately
NEBuffer 1
BSA
Tsp45I
NEBuffer 1BSA65Not Heat Inactivated
Catalog # Size Concentration Price Qty  
R0583L 1,000 units 4,000 units/ml $252.00
R0583S 200 units 4,000 units/ml $63.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Recognition Site:

GTSAC

isoschizomers | compatible ends | single letter code

Source:
Thermus species YS45 (R.A.D. Williams)

Reagents Supplied:
NEBuffer 1
BSA


Enzyme Properties


Activity in NEBuffers:
NEBuffer 1:100%
NEBuffer 2:25%
NEBuffer 3:0%
NEBuffer 4:75%

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:
10%

Heat Inactivation:
No

Survival in a Reaction:
Minimum units to digest 1 µg of substrate DNA in 16 hours: 0.50 unit(s)


Reaction & Storage Conditions


Reaction Conditions:
1X NEBuffer 1
Supplemented with 100 μg/ml Bovine Serum Albumin
Incubate at 65°C.

1X NEBuffer 1:
10 mM Bis-Tris-Propane-HCl
10 mM MgCl2
1 mM Dithiothreitol
pH 7.0 @ 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 65°C in a total reaction volume of 50 µl.

Concentration:
4,000 units/ml

Unit Assay Substrate:
λ DNA

Storage Conditions:
20 mM Tris-HCl
1 mM Dithiothreitol
0.1 mM EDTA
200 µg/ml BSA
50% Glycerol
0.15% Triton X-100
pH 7.4 @ 25°C

Storage Temperature:
-20°C

Diluent Compatibility:
Diluent A


FAQs


  1. Do degenerate recognition sites need to be palindromic?
  2. How can this enzyme be inactivated?

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 Tsp45I, > 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 Tsp45I.


16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA and 100 units of Tsp45I incubated for 16 hours at 65ºC 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 12 units of Tsp45I with 1 μg of a mixture of single and double-stranded [3H] E. coli DNA (205 cpm/μg) for 4 hours at 65ºC released < 0.5% of the total radioactivity.


Reagents Sold Separately


NEBuffer 1
BSA


Legal


Patents:
New England Biolabs, Inc.: U.S. Patent No. 5,866,422

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