The Cell Culture Media Preparation Facility (located in room 721 of the McArdle Laboratory) is under the faculty supervision of Dr. Janet Mertz. This 220 square foot facility is equipped with a laminar flow food, a water distillation apparatus, multiple filtration apparatuses, a balance, a pH meter, a 37 degree Celsius incubator, and several refrigerators. Ms. Kathy Johnson prepares and sterilizes cell culture media according to the needs of each investigator. Last year she prepared more than 3,800 liters of media; these media included DMEM with high glucose, Joklik, S-MEM, DMEM without phenol red, RPMI-1640 and F-12. Ms. Johnson also prepares special buffers and media such as DMEM lacking specific amino acids. She insures the sterility of each batch of medium by testing it for growth of contaminants and holding it for 3 to 4 weeks until all tests prove negative. During the last year, Ms. Johnson also prepared for bacterial and yeast work approximately 8,150 plates containing various nutrients, drugs, and indicators. These media are stored in 1/2 and 1 litter bottles in refrigerators located in room 721. Researchers throughout the McArdle Laboratory check out these media as needed, indicating the quantities taken so the costs of the ingredients can be charged back to the individual research groups.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA007175-35
Application #
6101409
Study Section
Project Start
1999-04-01
Project End
2000-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
35
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Thompson, Nancy E; Glaser, Bryan T; Foley, Katherine M et al. (2009) Minimal promoter systems reveal the importance of conserved residues in the B-finger of human transcription factor IIB. J Biol Chem 284:24754-66
Habig, Jeffrey W; Loeb, Daniel D (2006) Sequence identity of the direct repeats, DR1 and DR2, contributes to the discrimination between primer translocation and in situ priming during replication of the duck hepatitis B virus. J Mol Biol 364:32-43
Liu, Ning; Ji, Lin; Maguire, Megan L et al. (2004) cis-Acting sequences that contribute to the synthesis of relaxed-circular DNA of human hepatitis B virus. J Virol 78:642-9
Tessier, Charles R; Doyle, Glenn A; Clark, Brad A et al. (2004) Mammary tumor induction in transgenic mice expressing an RNA-binding protein. Cancer Res 64:209-14
Ostrow, Kristin M; Loeb, Daniel D (2004) Underrepresentation of the 3' region of the capsid pregenomic RNA of duck hepatitis B virus. J Virol 78:2179-86
Habig, Jeffrey W; Loeb, Daniel D (2003) Template switches during plus-strand DNA synthesis of duck hepatitis B virus are influenced by the base composition of the minus-strand terminal redundancy. J Virol 77:12412-20
Habig, Jeffrey W; Loeb, Daniel D (2003) The conformation of the 3' end of the minus-strand DNA makes multiple contributions to template switches during plus-strand DNA synthesis of duck hepatitis B virus. J Virol 77:12401-11
Bunger, Maureen K; Moran, Susan M; Glover, Edward et al. (2003) Resistance to 2,3,7,8-tetrachlorodibenzo-p-dioxin toxicity and abnormal liver development in mice carrying a mutation in the nuclear localization sequence of the aryl hydrocarbon receptor. J Biol Chem 278:17767-74
Liu, Ning; Tian, Ru; Loeb, Daniel D (2003) Base pairing among three cis-acting sequences contributes to template switching during hepadnavirus reverse transcription. Proc Natl Acad Sci U S A 100:1984-9
Mueller-Hill, Karlyn; Loeb, Daniel D (2002) cis-Acting sequences 5E, M, and 3E interact to contribute to primer translocation and circularization during reverse transcription of avian hepadnavirus DNA. J Virol 76:4260-6

Showing the most recent 10 out of 79 publications