AFFINITY GEL Detergent Removing Gel
| Catalog # | S119 |
|---|
Detergent Removing Gel has a low affinity for proteins and extraordinarily high affinity for detergents commonly employed for solubilization of membrane proteins. The principle of the gel is a combination of a powerful detergent binding liquid attached to a small pure matrix which excludes proteins having a molecular weight greater than 10,000 daltons. Protein detergent samples from pH 3-10 are efficiently stripped of detergents using this gel. The presence of 100 micromoles of phosphate and or 200 micromoles of sodium chloride will greatly enhance detergent binding to the gel.
Pricing & Ordering
| Quantity | Price | Action |
|---|---|---|
| 10ml gel + | $176.00 |
|
| 25ml gel + | $304.00 |
|
| 50ml gel + | $555.00 |
|
| 100ml gel + | $770.00 |
|
This detergent removing gel has a very low capacity for proteins and an extraordinarily high capacity for detergents commonly employed for solubilization of membrane proteins. The principle of the gel is a combination of a powerful detergent binding liquid attached to a small pure matrix which excludes proteins having a molecular weight greater than 10,000 daltons. Protein detergent samples from pH 3-10 are efficiently stripped of detergents using this gel. The presence of 100 micromoles of phosphate and or 200 micromoles of sodium chloride will greatly enhance detergent binding to the gel.
- Detergent Removing Gel has a low affinity for proteins and extraordinarily high affinity for detergents
- The gel is a combination of a powerful detergent binding liquid attached to a small pure matrix which excludes proteins greater than 10,000 daltons
- Protein detergent samples from pH 3-10 are efficiently stripped of detergents using this gel
- Adding 100 micromoles of phosphate and or 200 micromoles of sodium chloride will greatly enhance detergent binding to the gel
Articles about AFFINITY GEL
Detergent Removal for Protein Analysis: A Practical Technique Guide
Detergents help solubilize challenging protein samples, but they can complicate downstream assays and analytical readouts. This technique guide walks through…
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