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NEBuffer 3
BSA
AflIII
Cloned At NEBRecombinant SourceNEBuffer 3BSA37Heat Inactivated
Catalog # Size Concentration Price Qty  
R0541L 1,250 units 5,000 units/ml $244.00
R0541S 250 units 5,000 units/ml $61.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Recognition Site:

ACRYGT

isoschizomers | compatible ends | single letter code

Source:
A E. coli strain that carries the AflIII gene from Anabaena flos-aquae (CCAP 1403/13f).

Reagents Supplied:
NEBuffer 3
BSA


Enzyme Properties


Activity in NEBuffers:
NEBuffer 1:25%
NEBuffer 2:75%
NEBuffer 3:100%
NEBuffer 4:50%

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
More information about: Methylation Sensitivity

Heat Inactivation:
80°C for 20 minutes

Survival in a Reaction:
(+ + +) Suitable for an extended or overnight digestion. Enzyme is active > 8 hours.
More information about: Extended Digests with Restriction Enzymes


Reaction & Storage Conditions


Reaction Conditions:
1X NEBuffer 3
Supplemented with 100 μg/ml Bovine Serum Albumin
Incubate at 37°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 digest 1 µg of λ DNA in 1 hour at 37°C in a total reaction volume of 50 µl.

Concentration:
5,000 units/ml

Unit Assay Substrate:
λ DNA

Storage Conditions:
20 mM Tris-HCl
200 mM NaCl
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 B


FAQs


  1. Do degenerate recognition sites need to be palindromic?

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 5-fold overdigestion with AflIII, > 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 AflIII.


16-Hour Incubation:
A 50 μl reaction containing 1 μg of DNA and 50 units of AflIII 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 50 units of AflIII with 1 μg of a mixture of single and double-stranded [3H] E. coli DNA (205 cpm/μg) for 4 hours at 37ºC released < 0.2% of the total radioactivity.


Reagents Sold Separately


NEBuffer 3
BSA

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