A procedure has been described for the rapid and separate measurement of B12-binding α- and β-globulins using the batch technic. The method involves saturating B12-binders with Co57B12, removing excess radioactive B12 with a hemoglobin-coated charcoal pellet, and then separating the B12 binders using a pellet of DEAE cellulose, from which only the β-globulins are eluted in 0.06 M phosphate buffer at pH 6.35.

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