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1.the precipitate was dissolved in 20mM Tris-HCl buffer(PH7.4) and dialysed against the same buffer.

2.after 16h of dialysis, the sample was applied onto a ConA sepharose 4B column pre-equilibrated with equilibration buffer(20mM Tris-HCl, 1M NaCl,1mM CaCl2, MgCl2, MnCl2) at a flow rate of 0.1 ml/min.

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dialysed against the same buffer¾ÍÊÇÓÃͬÑùµÄ»º³åҺ͸Îö¡£
proteins in the supernatant were fractionated by ammonium sulphate precipitation(20%-60%)µÄÒâ˼ÊÇÉÏÇåÓÃ20-60%±¥ºÍ¶ÈÁòËáï§·Ö¼¶³Áµí£¬¼´ÓÃÁ½´Î³Áµí£¬ÏÈÓÃ20%µÄ³ÁµíÏ£¬ÊÕ¼¯ÉÏÇ壬ȻºóÔÙ¼ÓÁòËáï§ÖÁ60%±¥ºÍ¶ÈÔٴγÁµí£¬ÊÕ¼¯³Áµí¡£
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dialysed against the same buffer¾ÍÊÇÓÃͬÑùµÄ»º³åҺ͸Îö¡£
proteins in the supernatant were fractionated by ammonium sulphate precipitation(20%-60%)µÄÒâ˼ÊÇÉÏÇåÓÃ20-60%±¥ºÍ¶ÈÁòËáï§·Ö¼¶³Áµí£¬¼´ÓÃÁ½´Î³Á ...

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