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SalI-HF
SalI
Cloned At NEBRecombinant SourceTime SaverNEBuffer 3BSA37Heat InactivatedPass Blue White Selection Assay
Catalog # Size Concentration Price Qty  
R0138L 10,000 units 20,000 units/ml $224.00
R0138M 10,000 units 100,000 units/ml $224.00
R0138S 2,000 units 20,000 units/ml $56.00
R0138T 2,000 units 100,000 units/ml $56.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Recognition Site:

GTCGAC

isoschizomers | compatible ends | single letter code

Source:
A E. coli strain that carries the SalI gene from Streptomyces albus G (ATCC 49789).

Reagents Supplied:
NEBuffer 3
BSA


Enzyme Properties


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

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 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 (HindIII digest) in 1 hour at 37°C in a total reaction volume of 50 µl.

Concentration:
20,000 units/ml and 100,000 units/ml

Unit Assay Substrate:
λ DNA (HindIII digest)

Storage Conditions:
10 mM Tris-HCl
50 mM KCl
1 mM Dithiothreitol
0.1 mM EDTA
300 µg/ml BSA
50% Glycerol
pH 7.5 @ 25°C

Storage Temperature:
-20°C

Diluent Compatibility:
Diluent A


Notes


General notes:
  1. Conditions of low ionic strength, high enzyme concentration, glycerol concentration > 5%, or pH > 8.0 may result in star activity.
  2. GTm5CGAC is resistant to cleavage (in eukaryotes).
  3. When cleaving close to the end of DNA fragments, cleavage should be done at 37°C for 1 hour using 10 units/µg of DNA with a minimum of 3 bases on each side of the recognition sequence.
  4. Supercoiled forms of pBR322 and pUC require 10-fold overdigestion with SalI to achieve complete digestion.

FAQs


  1. Is SalI affected by methylation?
  2. Is SalI sensitive to pH?
  3. Is SalI affected by star activity?
  4. Are extended digestions with SalI recommended?
  5. Is SalI inhibited by nucleotides?
  6. Does SalI exhibit reduced activity on supercoiled DNA?
  7. What is the activity of SalI at 25°C?
  8. Does SalI have trouble cleaving PCR products?
  9. What is the molecular weight of SalI?
  10. Are more units of SalI required to cut supercoiled DNA than lambda DNA?
  11. Are SalI buffer and BamHI buffer identical?
  12. How many bases does SalI require for cleavage close to the ends?

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 40-fold overdigestion with SalI, > 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 SalI.


16-Hour Incubation:
A 50 μl reaction containing 1 μg of pBR322 DNA and 150 units of SalI 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 200 units of SalI 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.

Endonuclease Activity:
Incubation of a 50 μl reaction containing 40 units of SalI with 1 μg of ΦX174 RF I DNA for 4 hours at 37ºC resulted in < 20% 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 3
BSA


Companion Products


SalI-HF

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