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Establishment and characterization of a fibroblast cell line derived from Jining Black Grey goat for genetic conservation

机译:济宁黑灰山羊成纤维细胞遗传保护的建立与鉴定

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An ear marginal fibroblast cell bank was established from the Jining Black Grey (JBG) goat using attachment culture and freezing biotechniques. This bank included 32 ear samples (15 males and 17 females) and has stocks of 168 cryogenically preserved vials, each vial contained 4.0c10e cells per milliliter. The cells of the bank that were checked for the quality and the biological characteristics showed a typical fibroblast morphology when they cultured in vitro. The growth curve consisted of a growth curve consisting of a latent phase, logarithmic growth phase and stationary phase, cell population doubling time (PDT) of 48h. The chromosome analysis showed that the frequency of cells having the diploid number of chromosomes (60) was 98.65pl2.89%, and no microbe contamination (bacteria, epiphyte, virus or mycoplasma) was detected. In addition, lactate dehydrogenase (LDH) and malate dehydrogenase (MDH) zymography indicated that this cell bank was free of cross-contamination. At 24, 48 and 72h after transfection, the expression efficiency of pEGFP-C1, pEGFP-N3, pEYFP-N1, pECFP-N1, pECFP-mito and pDsRed1-N1 were between 11.8% and 56.3%. The fluorescence could be observed well-distributed in cytoplasm and nucleus except for some cryptomere vesicles at 24h after transfection. These newly established cell lines meet all the quality control standards established by the American Type Culture Collection. We have employed a new method for conserving the genetic resources of an important and endangered animal breed. The fibroblast bank that we have established from the JBG goat also provides an invaluable material resource for future studies that will utilize molecular and cell biology applications.
机译:使用附着培养和冷冻生物技术从济宁黑灰(JBG)山羊建立了耳朵边缘成纤维细胞库。该库包含32个耳朵样本(雄性15个,雌性17个),并有168个低温保存的小瓶,每个小瓶每毫升包含4.0c10e个细胞。在体外培养时,检查了库的细胞的质量和生物学特性的细胞显示出典型的成纤维细胞形态。生长曲线由潜伏期,对数生长期和静止期,细胞群倍增时间(PDT)48h组成的生长曲线组成。染色体分析表明,具有二倍体染色体数(60)的细胞的频率为98.65pl2.89%,并且没有检测到微生物污染(细菌,附生植物,病毒或支原体)。此外,乳酸脱氢酶(LDH)和苹果酸脱氢酶(MDH)酶谱表明该细胞库没有交叉污染。转染后24、48和72h,pEGFP-C1,pEGFP-N3,pEYFP-N1,pECFP-N1,pECFP-mito和pDsRed1-N1的表达效率在11.8%至56.3%之间。转染后24h,除了一些隐绒毛囊泡外,荧光在细胞质和细胞核中分布良好。这些新建立的细胞系符合美国典型培养物保藏中心建立的所有质量控制标准。我们采用了一种新方法来保护重要且濒临灭绝的动物品种的遗传资源。我们从JBG山羊那里建立的成纤维细胞库也为利用分子和细胞生物学应用的未来研究提供了宝贵的材料资源。

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