Bgl I

Product Details

Bgl I is a restriction enzyme purified from Bacillus globigii lacking BglII.

Reagents supplied: 10x BglI and 10x EQ buffer

Unit definition: One unit is the amount of enzyme required to digest 1 μg of Lambda DNA in 60 min at 37^oC in a total reaction volume of 50 μl.

Digest Guidelines

• Standard reaction conditions: In order to overcome DNA source variability, a ~10 fold overdigest is suggested:

10U Bgl I	1μl
10x EQ buffer	5μl
DNA substrate	1μg
Sterile ultrapure water	Up to 50 μl

• Speed Digest reaction: Incubate for 15 minutes at 37^oC as in standard reaction in 1x BglI buffer (100 mM KCl, 20 mM Tris-HCl (pH 8.5 @ 25°C), 10 mM MgCl2, 0.04% Triton X-100, 100 μg/ml BSA) or  1x eQ buffer (20 mM Tris-acetate (pH 7.9 @ 25^oC), 10 mM Mg-acetate, 50 mM K-acetate, 100 μg/ml BSA).

• Activity(%) in EnzyQuest buffers -Double digest tips

R1	R2	R3	R4	EQ
10-25	75-100	75-100	75-100	100

Reactions were performed as for unit definition reaction. The above data could be used as guideline for double digest reactions. Our enzymes are also active and compatible in buffer systems from other vendors.

Heat inactivation: 65^oC for 20 minutes

Methylation Sensitivity:

• dam methylation: Not sensitive
• dcm methylation: Not sensitive
• CpG methylation: Blocked by some combinations of overlapping

Unit calculation assay conditions:

• 1x BglI buffer
• Lambda DNA
• Incubation at 37^oC

Storage conditions:

• 300 mM NaCl
• 20 mM Tris-HCl (pH 7.5)
• 0.1 mM EDTA
• 1 mM dithiothreitol
• 500 μg/ml BSA
• 50% glycerol
• Store at -20^oC

Non-specific nuclease activity: 100 units of Bgl I do not produce any unspecific cleavage products after 16 hrs incubation with 1 μg of Lambda DNA at 37^oC.

Re-ligation and recut: After 50-fold overdigestion with Bgl I, greater than 95% of the DNA fragments can be ligated and recut with this enzyme.