Coated beads
A coating and molecular technology, applied in instruments, microcapsules, capsule delivery, etc., can solve the problems of reduced and completely denatured proteins lacking tertiary and secondary structures
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[0050] Coating of beads is conventional and well known in the art. That is, beads such as polystyrene beads are coated with an appropriate buffer, such as phosphate-buffered saline pH 7.2 or carbonate pH 9.6, which contains a typical concentration of 0.5-20ug / mL (depending on the protein) desired antigen or antibody and mixed gently at room temperature for 8-12 hours. The volume of buffer equals 50 μL / bead, so for 100,000 beads this equals 5000 mL. Excess coating solution is then usually aspirated off. Subsequent additions usually contain 50% Stabilcoat TM or Stabilguard TM of blocking / stabilizing buffer and mix for 30 min at room temperature, again using 50 μL / bead. Then discard most of the remaining blocking / stabilizing buffer. Typically, however, a small percentage of liquid remains, such as 2-5%. This was found to be necessary to allow the physical layer of the stabilizer to form a protective shell over the bound antigen / antibody. The beads and remaining liquid are ...
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