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Immunodepletion - Multiple Affinity Removal System
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Please select a topic from this section below:
Immunodepletion - Multiple Affinity Removal System
Click a question below to see the answer:
Albumin binds to other serum proteins. What other proteins will the Multiple Affinity Removal column remove?
What is the difference between the Multiple Affinity Removal LC Columns and Spin Cartridge capacity?
Can I check the Multiple Affinity Removal column capacity somehow?
Do you have custom Multiple Affinity Removal columns for larger volume injections?
Can I use the Multiple Affinity Removal System for human plasma or cerebrospinal fluid (CSF)?
Can I use the human Multiple Affinity Removal Column for mouse or rat serum?
Can the Multiple Affinity Removal System be used with any HPLC or FPLC instrument?
Has the column been tested with ''compromised'' plasma samples (e.g. hemolytic, lipimic, exteric)?
I need a 4.6 x 100 mm column for the high capacity. But, I think my sample loop is 100 µL size. What can I do?
My FPLC is in a cold room or cool box. Could column performance such as dynamic binding capacity be affected?
Can I get some information on the buffer content for the Multiple Affinity Removal System?
How can I get started using the Multiple Affinity Removal System?
Where can I get more technical information and ordering details for the Agilent Multiple Affinity Removal System?
Will the human protein depletion Multiple Affinity Removal LC Columns and Spin Cartridges work for any other species?
Do I need to exchange the buffer from my flow-through fraction?
Do the buffers have any detergents or surfactants in them?
Do I need to exchange buffer from my flow-through?
What is normal operating pressure? At what pressure should the frits be changed?
Should you expect to be able to detect the targeted proteins in the flow-though fraction?
How do you calculate which size column you need to end up with a certain amount of low abundance (flow through fraction) proteins?
Can I have any Triton X-100 or other detergent in the sample prior to injectin on the Multiple Affinity Column?
Can whole blood or blood spots be used with the Multiple Affinity Column or Spin Cartridges?
Can you use the flow-through and bound peak areas to calculate depletion efficiency?
