Tris Glycine-SDS Buffer 1x pH 8.3 (1000 ml) (10 pouches)
For Research Use Only
Protein electrophoresis under denaturing conditions (SDS-PAGE) involves separating proteins based on their size. By treating the sample under denaturing and reducing conditions with sodium dodecyl sulfate (SDS), proteins unfold and become coated with SDS detergent molecules, thereby acquiring a high net negative charge that is proportional to the length of their polypeptide chain. During electrophoresis, the negatively-charged protein molecules migrate towards the positive electrode and they are separated exclusively by size.
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Formulated from analytical grade chemicals.
Ideal for standardizing protein electrophoresis.
Exactly pre-weighed in pouches.
Ready to use in minutes.
|Chemicals: Analytical grade. |
Format: Exactly pre-weighed powder mix.
Volume: 1000 ml and 5000 ml.
Concentration: 0.025 M Tris, 0.192 M glycine, 0.10% SDS.
pH: 8.3 ± 0.2 at 25°C.
|Denaturing protein electrophoresis running buffer (SDS-PAGE).|
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