首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Evaluation of commercial chromatographic adsorbents for the direct capture of polyclonal rabbit antibodies from clarified antiserum
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Evaluation of commercial chromatographic adsorbents for the direct capture of polyclonal rabbit antibodies from clarified antiserum

机译:评价用于从澄清的抗血清中直接捕获多克隆兔抗体的商业色谱吸附剂

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We have carried out a rigorous evaluation of eight commercially available packed bed chromatography adsorbents for direct capture and purification of immumoglobulins from clarified rabbit antiserum. Three of these materials featured rProtein A (rProtein A Sepharose Fast Flow, Mabselect, Prosep rProtein A) as the affinity ligand, and differed from one another primarily with respect to the underlying base matrix. The remaining five matrices comprised various synthetic low molecular weight ligands immobilised on hydrophilic porous supports and these included: MEP HyperCel, MabSorbent AlP, MabSorbent A2P, FastMabsA and Kaptiv-GY. The general experimental approach taken was to sequentially challenge packed beds of each matrix with a series of different strengths of a clarified antiserum; beginning with the weakest and ending with the strongest. Marked differences in performance (principally evaluated on the basis of dynamic binding capacity, recovery, and purity) were obtained, which allowed clear recommendations concerning the choice of adsorbents best suited for antibody capture from rabbit antisera, to be made. (c) 2006 Elsevier B.V. All rights reserved.
机译:我们已经对八种市售填充床色谱吸附剂进行了严格的评估,以直接从澄清的兔抗血清中捕获和纯化免疫球蛋白。这些材料中的三种以rProtein A(rProtein A Sepharose Fast Flow,Mabselect,Prosep rProtein A)为亲和配体,并且主要区别在于基础基质。其余五种基质包括固定在亲水性多孔载体上的各种合成的低分子量配体,包括:MEP HyperCel,MabSorbent AlP,MabSorbent A2P,FastMabsA和Kaptiv-GY。采取的一般实验方法是用一系列不同强度的澄清抗血清依次攻击每种基质的填充床。从最弱开始,到最强结束。获得了明显的性能差异(主要根据动态结合能力,回收率和纯度进行了评估),这使得可以就最适合从兔抗血清中捕获抗体的吸附剂的选择提出明确的建议。 (c)2006 Elsevier B.V.保留所有权利。

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