Hi,
We try to work with cytometric bead array. We want to conjugate a protein to the beads, but everytime, the beads degradate during this procedure. Does somebody know, what can degradate these beads? And how long (and in which) can be the beads with conjugated protein stored (before the meassure)?
Thank you too much for the answers.
Problem with cytometric bead array
Started by marry, May 13 2012 12:11 PM
flow cytometry protein conjugatio CBA
No replies to this topic
Also tagged with one or more of these keywords: flow cytometry, protein conjugatio, CBA
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