Chromosome Location
NC_003552.1 (792605..793582)
Storage Buffer
Supplied as a liquid in 10mM Tris-HCl, pH 7.5, 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/ml BSA, 50% glycerol.
Unit Definition
One unit is defined as the amount of Bpl I required to digest 1ug of lambda DNA-Xhol in 1 hour at 37°C in 50ul of assay buffer (a maximal cleavage level is achieved at which no change in the fragmentation pattern is observed with further increase of enzyme).
Buffer Supplied
MBS638383 Restndion Enzyme Buffer A, lOX: 33mM Tns-acetate, pH 7.9, 10mM magnesium acetate,66mM potassium acetate, 0.1 mg/ml bSA
SAM: 0.05mM S-adenosylmethionine
Stability during Prolonged Incubation
A minimum of 0.3 units of Bpl l is required for complete digestion of 1 ug of DNA in 16 hours at 37°C.
Thermal Inactivation
Bpl l is inactivated by incubation at 65°C for 20 mins.
Methylation Effect
DAM, DCM, EcoKl, EcoBl: never overlaps no effect.
CpG: may overlap- no effect.
Number of Recognition Sites in DNA
Lambda: 1
PhiX174, M13mp1Sj19, pBR322,
pUC1S/19, pUCS7,
pTZ19R/U: 0
Digestion of Agarose-embedded DNA
A minimum of 10 units of Bpi l is required for complete digestion of 1 ug of agarose-embedded lambda DNA in 16 hours.
Overdigestion Assay
No detectable change in the specific fragmentation pattern is observed after 16D-fold overdigestion (10u/ug lambda DNA x 16 hours) with Bpll.
Ligation/Recutting Assay
The ligation and recreavage assay was replaced with LO test after validating experiments showed LO test ability10 trace nuclease and phosp,hatase activities with sensitivity that is higher thab L/R by a factor of 100.
Labeled Oligonucleotide (La) Assay
No detectable degradation of a single-stranded and double-stranded labeled oligonucleotide was observed after incubation with 10 units of Bpl I for 4 hours.
Blue/White Cloning Assay
The B/W assay was replaced with LO test after validating experiments showed LO test ability to aetect nuclease and phosphatase activities with sensitivity that equals to that of B/W test.