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Process for the pure presentation of the protease activating the blood coagulation factor VII, its proenzyme or a mixture of both proteins by means of ion exchange chromatography

机译:通过离子交换色谱纯呈递激活血凝因子VII的蛋白酶,其酶原或两种蛋白质的混合物的方法

摘要

A method is described for the purification of the protease activating the blood coagulation factor VII and / or its proenzyme, in which it is produced from biological or DOLLAR A) liquids produced by genetic engineering by means of anion or cation exchange chromatography at a pH below the isoelectric Point of the protein to be isolated or DOLLAR A b) by a combination of anion or cation exchange chromatography with affinity chromatography and / or fractional precipitation at pH values between 2.5 and 9.0, preferably between 2.5 and 7, 2 can be obtained, the affinity chromatography using DOLLAR A - calcium phosphate / hydroxylapatite, DOLLAR A - a hydrophobic matrix, DOLLAR A - a chelating matrix, DOLLAR A - a matrix which is combined with an immobilized or directed against the protein to be isolated, monoclonal or polyclonal antibody or its F (ab) or F (ab) 2 fragments ten coated is carried out. DOLLAR A A pharmaceutical preparation and a reagent are also described which contain the protease and / or its proenzyme.
机译:描述了一种用于纯化激活血液凝结因子VII和/或其蛋白酶的蛋白酶的方法,其中所述蛋白酶是由通过遗传工程通过阴离子或阳离子交换色谱法在低于pH的pH的生物或DOLLAR A)液体中产生的。通过将阴离子或阳离子交换色谱法与亲和色谱法和/或在pH值介于2.5和9.0之间,优选在2.5和7之间的部分沉淀相结合,可以得到待分离蛋白质或DOLLAR A b)的等电点,使用DOLLAR A-磷酸钙/羟基磷灰石,DOLLAR A-疏水性基质,DOLLAR A-螯合基质,DOLLAR A-与固定化或针对待分离蛋白的基质,单克隆或多克隆抗体结合的亲和色谱或对其F(ab)或F(ab)2片段进行十次包被。美元A还描述了包含蛋白酶和/或其原酶的药物制剂和试剂。

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