THE CULTURE OF RAT MYELOMA AND RAT HYBRIDOMA CELLS IN A PROTEIN-FREE MEDIUM

被引:6
作者
KEEN, MJ
机构
[1] Biology Research Division, Wellcome Research Laboratoires, Beckenham, Kent, Langley Court
关键词
Y0; HYBRIDOMA; MYELOMA; PROTEIN-FREE; CULTURE MEDIUM;
D O I
10.1007/BF00749657
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Y0 is a rat x rat hybridoma cell line, which does not secrete immunoglobulin, produced using a fusion partner derived from the Y3 (Y3,Ag.1.2.3) rat myoloma cell line. Y0 and Y3 have both been widely used as fusion partners in the production of rat x rat hybridomas. Y0 has also been used in recombinant gene technology. Y0 cells grown in shake flask culture, using RPMI 1640 medium with 4mM l-glutamine and 5% foetal bovine serum, reached a maximal cell density of 1.5 x 10(6) cells ml(-1) with 86% viability. Y0 cells which had been adapted to grow in ABC protein-free medium reached a maximal density, in shake flask culture, of 8.75 x 10(5) cells ml(-1) with 79% viability. An improved protein-free medium, designated W38 medium, was developed. In shake flask culture, W38 medium supported Y0 cell growth to a density of 2.02 x 10(6) cells ml(-1) with 96% viability. Two Y3 hybridomas, YID 13.9.4 cells and SAM 618 cells were adapted to growth in W38 medium. For both hybridomas, cell growth and product yield in shake flask culture using W38 medium was superior to that obtained with serum-containing RPMI 1640 medium.
引用
收藏
页码:193 / 202
页数:10
相关论文
共 20 条
[1]  
CLEVELAND WL, 1983, J IMMUNOL METHODS, V56, P221
[2]   A SIMPLE METHOD FOR MEASURING PATIENT ANTI-GLOBULIN RESPONSES AGAINST ISOTYPIC OR IDIOTYPIC DETERMINANTS [J].
COBBOLD, SP ;
REBELLO, PRUB ;
DAVIES, HFS ;
FRIEND, PJ ;
CLARK, MR .
JOURNAL OF IMMUNOLOGICAL METHODS, 1990, 127 (01) :19-24
[3]  
DARFLER FJ, 1990, IN VITRO CELL DEV BI
[4]   PLAQUE PRODUCTION BY THE POLYOMA VIRUS [J].
DULBECCO, R ;
FREEMAN, G .
VIROLOGY, 1959, 8 (03) :396-397
[5]   RAT-X-RAT HYBRID MYELOMAS AND A MONOCLONAL ANTI-FD PORTION OF MOUSE IGG [J].
GALFRE, G ;
MILSTEIN, C ;
WRIGHT, B .
NATURE, 1979, 277 (5692) :131-133
[6]  
HALE G, 1988, LANCET, V2, P1394
[8]  
JOYCE C, 1990, THESI U LONDON
[9]  
KEEN MJ, 1995, CYTOTECHNOLOGY
[10]  
KENTEN JH, 1986, Patent No. 216846