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通过制备型平板等速电泳分离Fc结合血清蛋白。

Separation of Fc-binding serum proteins by preparative flat-bed isotachophoresis.

作者信息

Nicolaisen E M, Brogren C H

出版信息

J Immunol Methods. 1982 Oct 29;54(2):165-73. doi: 10.1016/0022-1759(82)90057-6.

Abstract

Preparative flat-bed isotachophoresis with discrete spacers was applied as a single-step procedure to separate 2 Fc-dependent activities of normal chicken serum, i.e., (1) the ability to raise the titre of haemagglutinating allo-antisera which is due to a high molecular weight beta-globulin (HEF), (2) the ability to activate guinea pig complement components in mixed complement reaction. The results demonstrate that the 2 activities can be clearly separated, and HEF must therefore be different from the first complement factor in the chicken. Under the chosen conditions the molecule active in the mixed complement reaction is not stacked in contrast to other serum protein including HEF. The same technique with human serum shows that human Clq behaves in the same was as the chicken complement factor. This means that by selective unstacking, flat-bed isotachophoresis can be used as an efficient single-step purification method for human and chicken Clq.

摘要

采用带有离散间隔物的制备型平板等速电泳作为单步程序,以分离正常鸡血清中两种依赖Fc的活性,即:(1)提高血凝同种抗血清滴度的能力,这归因于一种高分子量β球蛋白(HEF);(2)在混合补体反应中激活豚鼠补体成分的能力。结果表明,这两种活性可以清晰分离,因此HEF必定与鸡的第一补体因子不同。在所选择的条件下,与包括HEF在内的其他血清蛋白不同,在混合补体反应中具有活性的分子不会堆积。对人血清采用相同技术表明,人Clq的行为与鸡补体因子相同。这意味着,通过选择性去堆积,平板等速电泳可作为人及鸡Clq的高效单步纯化方法。

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