BglI restriction enzyme product blog
Tags: Restriction Enzyme; BglI; BglI restriction enzyme;
The BglI n/a (Catalog #MBS638401) is a Restriction Enzyme produced from Bacillus globigii and is intended for research purposes only. The product is available for immediate purchase.The BglI n/a product has the following accession number(s) (GI #54660748) (NCBI Accession #AAV37465.1). Researchers may be interested in using Bioinformatics databases such as those available at The National Center for Biotechnology Information (NCBI) website for more information about accession numbers and the proteins they represent. Even researchers unfamiliar with bioinformatics databases will find the NCBI databases to be quite user friendly and useful.
To buy or view more detailed product information and pricing, please click on the technical datasheet page below:
Please refer to the product datasheet for known applications of a given restriction enzyme. We\'ve tested the BglI with the following immunoassay(s):
Testing Data ()
5\'-G C C N N N N^N G G C-3\'.
Dilution Buffer: 10mM Tris-HCl (pH 7.4 at 25 degree C), 100mM KCl, 1mM EDTA, 1mM DTT, 0.2mg/ml BSA and 50% glycerol. For longer periods-the Storage Buffer should be used.
Digestion of Agarose-embedded DNA: A minimum of 5units of enzyme is required for digestion of 1ug of agarose-embedded lambda DNA in 16 hours.
Methylation Effects: The hemi-methylated sequence GCCN5GGm5C is cleaved by BglI at a significantly slower rate. Cleavage is blocked when both strands are methylated at positions: 5\'� GCCN5GGm5C�3\' 3\'�m5CGGN5CC G�5\'. Overlapping CG methylation may influence DNA cleavage.
pACYC177: 1
pACYC184: 2. Labeled Oligonucleotide (LO) Assay: No detectable degradation of a single-stranded and double-stranded labeled oligonucleotide was observed after incubation with 10units of restriction endonuclease for 4 hours.
Lambda: 29
Ligation/Recutting Assay: After 50-fold overdigestion (3u/ug DNA x 17 hours) with BglI, more than 95% of the DNA fragments can be ligated at a 5\'-termini concentration of 0.3uM. More than 95% of these can be recut.
M13mp18/19: 1
Overdigestion Assay: No detectable change in the specific fragmentation pattern is observed after 160-fold overdigestion (10u/ug lambda DNA x 16 hours) with BglI.
pBR322: 3
PhiX174: 0
pTZ19R/U: 2
pUC18/19: 2
pUC57: 2
Stability During Prolonged Incubation: A minimum of 0.1units of enzyme is required for complete digestion of 1ug of lambda DNA in 16 hours at 37 degree C.
Storage Buffer: 10mM Tris-HCl (pH 7.5 at 25 degree C), 300mM NaCl, 1mM DTT, 0.1mM EDTA, 0.2mg/ml BSA and 50% glycerol.
Thermal Inactivation: Enzyme is inactivated by incubation at 65 degree C for 20min.
Unit Definition: One unit is defined as the amount of enzyme required to digest 1ug of lambda DNA in 1 hour at 37 degree C in 50ul of assay buffer.