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作 者:乔自林[1] 冯若飞[1] 李明生[1] 冯玉萍[2] 暴艳敏 姚敏香[2]
机构地区:[1]西北民族大学生物工程与技术国家民委重点实验室,甘肃兰州730030 [2]西北民族大学生命科学与工程学院,甘肃兰州730030 [3]兰州民海生物工程有限公司,甘肃兰州730010
出 处:《西北民族大学学报(自然科学版)》2008年第3期53-55,70,共4页Journal of Northwest Minzu University(Natural Science)
摘 要:用含不同浓度的牛源性血红蛋白细胞培养液培养小鼠骨髓瘤细胞,通过细胞计数绘制生长曲线,计算最大增殖浓度和倍增时间。并进行比较分析.结果表明:当培养液的血红蛋白浓度在1-5rag/dL时小鼠骨髓瘤细胞生长较好,细胞最大增殖浓度在1.2×10^6/mL以上,倍增时间小于20h,当培养液的血红蛋白浓度为6mg/dL时细胞生长抑制,细胞最大增殖浓度和倍增时间为6.7×10^5/mL和21.6h.由此可见,培养液中血红蛋白浓度≤5mg/dL时不影响细胞生长,达到6mg/dL时抑制细胞生长.SP2/0 - Ag14 cells were seeded in cell cultures which contained the different concentrations of hemoglobin from bovine blood. By means of accounting the number of SP2/0 - Ag14 cells, the growth curves were made and the Max proliferation concentration and population doubling time were analyzed. The results showed that at 1- 5 mg/dL concentration of hemoglobin, the SP2/0 - Ag14 cells grew well, and the Max proliferation concentration was more than 1.2 ×10^6 cell/mL, and the population doubling time appeared before 20 hours. When in cell culture the concentration of hemoglobin was over 6 mg/dL, the SP2/0 - Agl4 cell growth was arrested, the Max proliferation concentration were 6.7 ×10^5 cell/mL and the population doubling time was 21.6 hours. The concentration of hemoglobin which was lower than 5 mg/dL failed to affect the SP2/0 - Ag14 cell growth. However, one reaching 6mg/dL could restrict the growth of SP2/0 - Ag14.
关 键 词:血红蛋白 细胞培养 SP2/0-Ag14
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