missing translation for 'onlineSavingsMsg'
Learn More
Learn More
OPTIZYME™ XbaI, Fisher BioReagents™
Brand: Fisher BioReagents BP8008-5
This item is not returnable.
View return policy
Description
5'...T^C T A G A...3'
3'...A G A T C^T...5'
Supplied with: 10X OPTIZYME Buffer 4
Conditions for 100% Activity
- 1X OPTIZYME Buffer 4: 33mM Tris-acetate (pH 7.9 at 37°C), 10mM Mg-acetate, 66mM K-acetate and 0.1mg/ml BSA
- Incubate at 37°C
- Buffer 1: 50 - 100%
- Buffer 2: 50 - 100%
- Buffer 3: 20 - 50%
- Buffer 4: 100%
- Buffer 5: 0 - 20%
10mM Tris-HCl (pH 7.4 at 25°C), 100mM KCl, 7mM 2-mercaptoethanol, 1mM EDTA, 0.2mg/ml BSA and 50% (v/v) glycerol
Ligation and Re-cleavage:
More than 95% of the DNA fragments can be ligated and re-cut after a 50-fold over-digestion with XbaI.
Digestion of Agarose-embedded DNA:
A minimum 5 units of XbaI is required for the complete digestion of 1μg of agarose-embedded lambda DNA in 16 hours.
Notes:
- XbaI is blocked by overlapping dam methylation.
- To avoid dam methylation, use a dam-, dcm- strain.
Methylation Effects:
Dam: May overlap - blocked
- 5'...TCTAGm6A TC...3'
- 3'...AGATC Tm6AG...5'
- (Cleavage is blocked)
CpG: Never overlaps - no effect
EcoKI: Never overlaps - no effect
EcoBI: Never overlaps - no effect
Specifications
50 U/μL | |
37°C | |
Indicates ligation efficiency of DNA fragments generated by digestion with the Restriction Enzyme | |
10,000 U | |
XbaI |
10X OPTIZYME™ Buffer 4 | |
7.4 | |
10mM Tris HCl (pH 7.4), 100mM KCl, 7mM 2-mercaptoethano, 1mM EDTA, 0.2mg/mL BSA, 50% Glycerol | |
T.CTAGA | |
Liquid |
Safety and Handling
Product Identifier
- OPTIZYME
Product Content Correction
Your input is important to us. Please complete this form to provide feedback related to the content on this product.
Product Title
Spot an opportunity for improvement?Share a Content Correction