Mahassni Sawsan H, Klapper David G, Hiskey Richard G
Department of Biochemistry, King Abdulaziz University, Jeddah, Saudi Arabia.
Hybridoma (Larchmt). 2009 Jun;28(3):189-97. doi: 10.1089/hyb.2008.0087.
An IgM monoclonal antibody, S11-23.4, raised against the 47-62 amino acid sequence in bovine prothrombin fragment 1 (F-1, the amino-terminal 156 residues of prothrombin), was purified from tissue culture supernatants and ascites using different purification schemes to determine the best method. There are many different purification schemes for the purification of IgG antibodies, which are generally easier to purify than IgM antibodies. Several different methods and schemes were tried to purify S11-23.4, and it was determined that the best purification schemes are ion exchange chromatography for cell culture IgM antibodies, and a G-100 gel filtration column, in conjunction with precipitation, reduction, and alkylation, for the same IgM antibody in ascites.
一种抗牛凝血酶原片段1(F-1,凝血酶原氨基末端156个残基)中47-62氨基酸序列产生的IgM单克隆抗体S11-23.4,使用不同的纯化方案从组织培养上清液和腹水中进行纯化,以确定最佳方法。对于IgG抗体的纯化有许多不同的纯化方案,其通常比IgM抗体更容易纯化。尝试了几种不同的方法和方案来纯化S11-23.4,确定最佳的纯化方案是用于细胞培养IgM抗体的离子交换色谱法,以及用于腹水中相同IgM抗体的G-100凝胶过滤柱,结合沉淀、还原和烷基化。