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1 of six hFSH isoform preparations derived by chromatofocusing.
2 concanavalin A affinity chromatography, and chromatofocusing.
3 eing dominant, were observed in pericytes by chromatofocusing.
4 ysiological fluids are commonly separated by chromatofocusing.
5 arose, hydroxyapatite, phenyl-Sepharose, and chromatofocusing.
6 pitation, anion exchange chromatography, and chromatofocusing.
7 ium sulfate precipitation, ion-exchange, and chromatofocusing.
8 y concanavalin-A affinity chromatography and chromatofocusing.
12 no Q, hydroxylapatite, phenyl-Sepharose, and chromatofocusing fast protein liquid chromatography from
15 ificantly improved performance that gradient chromatofocusing has in protein separations compared to
16 sults are compared with that of conventional chromatofocusing in the chromatography of several protei
20 lar sieve chromatography on Sephacryl S-100, chromatofocusing on Polybuffer exchanger 94, and affinit
21 ins was achieved in less than 20 min using a chromatofocusing resin and two buffers in a microcentrif
25 ses from inherent advantages in the gradient chromatofocusing technique in optimizing conditions pert
26 in peak width achieved with the pH gradient chromatofocusing technique through the manipulation of b
27 , anion-exchange column packings are used in chromatofocusing to demonstrate the resolution and speed
28 involves fractionation according to pI using chromatofocusing with analytical columns in the first di
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