Given below are a few of the essential "do’s and don'ts" of cell culture. Some of these are mandatory e.g. use of personal protective equipment (PPE). Many of them are common sense and apply to all laboratory areas. However some of them are specific to tissue culture.
The Do’s
Use personal protective equipment, (laboratory coat/gown, gloves and eye protection) at all times. In addition, thermally insulated gloves, full-face visor and splash-proof apron should be worn when handling liquid nitrogen.
Always use disposable caps to cover hair.
Wear dedicated PPE for tissue culture facility and keep separate from PPE worn in the general laboratory environment. The use of different colored gowns or laboratory coats makes this easier to enforce.
Keep all work surfaces free of clutter.
Correctly label reagents including flasks, medium and ampules with contents and date of preparation.
Only handle one cell line at a time. This common-sense point will reduce the possibility of cross contamination by mislabeling etc. It will also reduce the spread of bacteria and mycoplasma by the generation of aerosols across numerous opened media bottles and flasks in the cabinet.
Clean the work surfaces with a suitable disinfectant (e.g. 70% ethanol) between operations and allow a minimum of 15 minutes between handling different cell lines.
Wherever possible maintain separate bottles of media for each cell line in cultivation.
Examine cultures and media daily for evidence of gross bacterial or fungal contamination. This includes medium that has been purchased commercially.
Quality Control all media and reagents prior to use.
Keep cardboard packaging to a minimum in all cell culture areas.
Ensure that incubators, cabinet, centrifuges and microscopes are cleaned and serviced at regular intervals.
Test cells for mycoplasma on a regular basis.
The Don’ts
Do not continuously use antibiotics in culture medium as this will inevitably lead to the appearance of antibiotic resistant strains and may render a cell line useless for commercial purposes.
Don’t allow waste to accumulate particularly within the microbiological safety cabinet or in the incubators.
Don't have too many people in the lab at any one time.
Don't handle cells from unauthenticated sources in the main cell culture suite. They should be handled in quarantine until quality control checks are complete.
Avoid keeping cell lines continually in culture without returning to frozen stock.
Avoid cell culture becoming fully confluent. Always sub-culture at 70-80% confluency or as advised on ECACC's cell culture data sheet.
Do not allow media to go out of date. Shelf life is only 6 weeks at +4ºC once glutamine and serum is added.
Avoid water baths from becoming dirty by using Sigma Clean (Prod. No. S5525).
Don’t allow essential equipment to become out of calibration. Ensure microbiological safety cabinets are tested regularly.
文|《中国科学报》记者李思辉实习生何睿她是一位知名三甲医院的科室主任:不仅负责科室的管理工作,而且每周4个半天坐诊,每年主刀800多台手术;她是院士师门的“大师姐”:繁忙的临床工作之余,做研究、带学生......
Fanzor(Fz)是一种广泛存在于真核生物结构域的ωRNA引导内切酶,具有独特的基因编辑潜力。2024年8月28日,麻省理工学院/博德研究所张锋团队在Cell在线发表题为“Structuralins......
叶绿体蛋白在ATP酶马达的驱动下,通过叶绿体外膜(TOC)转座子和叶绿体内膜(TIC)超复合体的转座子导入。Ycf2-FtsHi复合体已被确定为叶绿体进口马达。然而,其在前蛋白转运过程中与TIC复合物......
日前,国产期刊TheInnovation获得首个影响因子(IF=32.1),成为科睿唯安JCR综合性期刊分类下排名仅次于《自然》(IF=64.8)和《科学》(IF=56.9)的期刊,并且这本期刊在目前......
文| 《中国科学报》记者李思辉实习生毕若雪“2021年暑假的一个凌晨,我突然灵机一动,思考了很久的一个模型突然清晰起来。我立即从床上蹦起来,花了5分钟,在纸上把它清楚地画了出来!”说起最近发......
“一稿多投”一直被认为是不端的行为,但这个“规矩”是在纸质时代信息沟通不畅的情况下制定的,近年来广大作者呼吁取消这一观念的声音已振聋发聩!让人欣喜的是,截止目前,已经有两大国际知名出版社响应了这一呼吁......
2024年4月23日,北京理工大学生命学院肖振宇副教授、中国科学院动物研究所王红梅、于乐谦、郭靖涛研究员、中国农业大学魏育蕾教授、郑州大学第一附属医院何南南助理研究员在国际学术期刊Cell发表文章《3......
2019年10月3日,加州大学圣地亚哥分校BrendaL.Bloodgood团队(G.StefanoBrigidi为第一作者)在Cell在线发表题为“GenomicDecodingofNeuronal......
美国宾夕法尼亚大学佩雷尔曼医学院科研人员发现,蚂蚁的血脑屏障在控制其行为方面起着积极的作用。血脑屏障可以调节蚂蚁大脑中的激素水平,从而影响他们在蚁群中的行为。相关研究成果发表在《Cell》杂志上。研究......
RNA引导系统利用引导RNA和靶核酸序列之间的互补性来识别遗传元件,在原核生物和真核生物的生物过程中都起着核心作用。例如,原核CRISPR-Cas系统为细菌和古细菌提供了对外来遗传因子的适应性免疫。C......