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Problem with cytometric bead array

flow cytometry protein conjugatio CBA

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#1 marry



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Posted 13 May 2012 - 12:11 PM


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.

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