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Purification and characterization of immunoglobulin production stimulating factor derived from human B lymphoblastoid HO-323 cells

机译:人B淋巴母细胞HO-323细胞产生的免疫球蛋白刺激因子的纯化和鉴定

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摘要

An immunoglobulin (Ig) production stimulating factor (IPSF) for hybridomas was found in spent medium of the human B lymphoblastoid cell line, HO-323. The IPSF was purified by serial use of DEAE chromatography, ultrafiltration, gel filtration and HPLC-DEAE chromatography. Purified IPSF was estimated to be a 410 k macro molecule by gel filtration, and contained three types of isomers which were separated from each other by native polyacrylamide gel electrophoresis. All of the isomers were, however, assumed to have the same protein components by SDS polyacrylamide gel electrophoresis.The IPSF was effective for human-human and mouse-mouse hybridomas producing IgM, but not for IgG producers in the experimental condition used here. Human-human hybridoma HF10B4, cultured in IPSF-containing medium, produced 20 times more IgM than in IPSF-free medium under serum-free conditions. The IPSF showed very little proliferation stimulating activity on HF10B4 cells.
机译:在人类B淋巴母细胞系HO-323的废培养基中发现了杂交瘤的免疫球蛋白(Ig)产生刺激因子(IPSF)。通过连续使用DEAE色谱法,超滤,凝胶过滤和HPLC-DEAE色谱法纯化IPSF。通过凝胶过滤,纯化的IPSF估计为410k大分子,并且包含通过天然聚丙烯酰胺凝胶电泳彼此分离的三种类型的异构体。然而,通过SDS聚丙烯酰胺凝胶电泳假定所有异构体具有相同的蛋白质成分.IPSF对产生IgM的人-人和小鼠-小鼠杂交瘤有效,但在此处使用的实验条件下对IgG产生者无效。在不含血清的条件下,在含IPSF的培养基中培养的人-人杂交瘤HF10B4产生的IgM比不含IPSF的培养基高20倍。 IPSF对HF10B4细胞几乎没有增殖刺激活性。

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