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Invitrogen™ Novex™ TBE Running Buffer (5X)
Description
Novex™ TBE Gels provide highest resolution possible for analyzing restriction digests and PCR products. DNA fragments ranging from 10 to 3,000 base pairs are clearly resolved into sharp, tight bands.
- Prepared with 0.5X TBE as gel buffer
- Sufficient for good electrophoretic separation, yet low enough to promote DNA-protein interactions
- TBE and DNA Retardation Gels are designed to run on the XCell SureLock™ Mini-Cell
Acrylamide Gel Electrophoresis, DNA & RNA Purification & Analysis, Nucleic Acid Gel Electrophoresis & Blotting
Order Info
Shipping Condition: Room Temperature
Specifications
Specifications
| Buffer | Running Buffer |
| Concentration | 5 X |
| Content And Storage | Store at room temperature |
| Gel Compatibility | Polyacrylamide Gels, Agarose Gels |
| For Use With (Application) | Nucleic Acid Gel Electrophoresis, Blotting |
| Product Line | Novex |
| Product Type | TBE Running Buffer |
| Quantity | 1 L |
| Shipping Condition | Room Temperature |
Frequently Asked Questions (FAQs)
If a slight turbidity develops, the fine precipitate can be dissolved by autoclaving for 5 minutes at 110°C. Do not autoclave in the container supplied. This treatment has no deleterious effect on the buffering properties of TBE.
Please see the recipes below:
TBE Running Buffer (5X):
Tris base, 54.0 g
Boric acid, 27.5 g
EDTA (free acid), 2.9 g
Deionized water to 1.0 L
Hi-Density TBE Sample Buffer (5X):
5X TBE Running buffer (Cat. No. LC6675), 2 mL
Ficoll Type 400, 1.5 g
Bromophenol blue, 1 mL of 1% solution
Xylene cyanol 1 mL of 1% solution
Deionized water to 10.0 mL
For Research Use Only. Not for use in diagnostic procedures.