Purpose
To describe the preparation of a Master Cell Bank
Safety
See SP 09-001 for lab safety considerations for the cell culture lab.
Equipment
Laminar Flow Hood
Freezers, -70oC or Rate-Controlled Freezer
Liquid Nitrogen Freezer
Materials
Cryovials, 1.8 ml (Nunc or equivalent)
Cryovial rack (Nunc or equivalent)
Sterile Centrifuge tubes, 50 ml (VWR # 21008-146 or equivalent)
Fetal Bovine Serum, heat inactivated (BioWhittaker # 14-503F or equivalent)
Sterile DMSO (Sigma # D2650 or equivalent)
Sterile Pipets of appropriate sizes
Ice
Permanent Marking Pen
Lab Coat
Latex Gloves
70 % alcohol or equivalent
Trypan Blue, 0.4% (GIBCO # 630-5250AG or equivalent)
Hemocytometer
Nunc Freezing Container (# 5100-0001)
Freezer Log
Procedure
The Master Cell Bank consists of 20 vials of cells at 5 x 106 cells/vial.
Before preparing the Master Cell Bank, ensure that the cell line is stabilized and that the cells are free from mycoplasma contamination.
The day before freezing, refeed the cells with fresh medium, or add additional medium to suspension cultures to ensure that they are in log phase of growth.
Chill the Freezing medium on ice.
Label with cryotubes with the cell line name, the cells/vial, and the date. Include on the label that the vials are the Master Cell Bank. Place the vials in the cryotube rack and place the rack on ice.
Prepare a single cell suspension, use trypsin for adherent cell line.
Take an aliquot for a cell count. Count the cells using a hemocytometer, according to the current revision of SP 05-009. Determine the viability using trypan blue stain, according to the current revision of SP 09-005. NOTE: The cells must have greater than 90% viability before proceeding. If the cells are less than 90% viability, do not freeze.
Transfer the cell suspension to centrifuge tubes.
Centrifuge at 1000 rpm for 5 minutes, 2-8oC.
Siphon off all the medium.
Slowly add chilled freezing medium to yield 5 x 106 cells/ml. Resuspend the cells in the freezing medium by gently pipetting.
Place the tube on ice. Dispense the cells, 1 ml/vial, into the labeled cryovials. Recap vials tightly. Complete all vials.
Place the vials into the Nunc Freezing Container or Rate Controlled Freezer Racks.
Replace the lid on the freezing container. Place the Freezing Container in the -700C Freezer overnight.
Transfer the vials to the vapor phase of the liquid nitrogen freezer.
Record the cell line information and location in the Freezer Log.
文|《中國科學報》記者李思輝實習生何睿她是一位知名三甲醫院的科室主任:不僅負責科室的管理工作,而且每周4個半天坐診,每年主刀800多臺手術;她是院士師門的“大師姐”:繁忙的臨床工作之余,做研究、帶學生......
Fanzor(Fz)是一種廣泛存在于真核生物結構域的ωRNA引導內切酶,具有獨特的基因編輯潛力。2024年8月28日,麻省理工學院/博德研究所張鋒團隊在Cell在線發表題為“Structuralins......
葉綠體蛋白在ATP酶馬達的驅動下,通過葉綠體外膜(TOC)轉座子和葉綠體內膜(TIC)超復合體的轉座子導入。Ycf2-FtsHi復合體已被確定為葉綠體進口馬達。然而,其在前蛋白轉運過程中與TIC復合物......
文| 《中國科學報》記者李思輝實習生畢若雪“2021年暑假的一個凌晨,我突然靈機一動,思考了很久的一個模型突然清晰起來。我立即從床上蹦起來,花了5分鐘,在紙上把它清楚地畫了出來!”說起最近發......
“一稿多投”一直被認為是不端的行為,但這個“規矩”是在紙質時代信息溝通不暢的情況下制定的,近年來廣大作者呼吁取消這一觀念的聲音已振聾發聵!讓人欣喜的是,截止目前,已經有兩大國際知名出版社響應了這一呼吁......
2024年4月23日,北京理工大學生命學院肖振宇副教授、中國科學院動物研究所王紅梅、于樂謙、郭靖濤研究員、中國農業大學魏育蕾教授、鄭州大學第一附屬醫院何南南助理研究員在國際學術期刊Cell發表文章《3......
2019年10月3日,加州大學圣地亞哥分校BrendaL.Bloodgood團隊(G.StefanoBrigidi為第一作者)在Cell在線發表題為“GenomicDecodingofNeuronal......
美國賓夕法尼亞大學佩雷爾曼醫學院科研人員發現,螞蟻的血腦屏障在控制其行為方面起著積極的作用。血腦屏障可以調節螞蟻大腦中的激素水平,從而影響他們在蟻群中的行為。相關研究成果發表在《Cell》雜志上。研究......
RNA引導系統利用引導RNA和靶核酸序列之間的互補性來識別遺傳元件,在原核生物和真核生物的生物過程中都起著核心作用。例如,原核CRISPR-Cas系統為細菌和古細菌提供了對外來遺傳因子的適應性免疫。C......
大約700萬年前,人類從我們最接近的動物親戚黑猩猩那里分離出來,在進化樹上形成了我們自己的分支。在此后的時間里---從進化的角度看是短暫的---我們的祖先進化出了使我們成為人類的性狀,包括比黑猩猩大得......