The mission of the Cell Biology & Microinjection component of Reproductive Sciences is to provide CancerCenter members with access to centralized facilities, instrumentation and technical expertise necessary toallow investigators to carry out embryonic stem (ES) cell line derivation, electroporation, and to creategenetically modified mice for in vivo studies of gene function. The Service generates genetically modifiedmice on a variety of inbred strain and hybrid backgrounds and has derived germline-competent ES celllines from inbred mouse strains. Germline-competence validation, training, custom projects, and testedreagents and supplies are also offered. The Service, which has previously been supported by CancerCenter support grant (CCSG) funds, works closely with Cryopreservation, Importation and Rederivationwithin Reproductive Sciences, as well as Phenotyping Sciences to provide Cancer Center members wellintegrated comprehensive services. In 2004 the Cell Biology & Microinjection Service merged with theReproductive Technologies Resource to form Reproductive Sciences. The synergy created by the mergerallowed management and staff to identify complementary and overlapping functions within the groups;establish new collaborative service offerings; merge similar processes to eliminate redundancy; andcombine laboratory, vivarium and office space to maximize productivity. Cell Biology & MicroinjectionService personnel work closely with other members of Reproductive Sciences and the Molecular BiologyService to offer Cancer Center investigators seamless access to services. This close internal collaborationinsures that investigators with expertise outside of these areas can fully employ current transgenic andgene targeting technology in their own work by utilizing these interactive services. Senior Staff Scientist Dr.Thomas Gridley was named Faculty Advisor (Project Leader) of Cell Biology & Microinjection Service in1999. He oversees this fee-for-service operation which employs two ES cell technologists, twomicroinjection technologists, a colony manager and senior operational manager. The Service occupies1,899 ft2 of laboratory, vivarium and office space in Research Laboratory Building 4 and the GeneticsResources Building. Dr. Gridley communicates with the Cancer Center users, Service staff and CenterAdministration to ensure that research needs are met in the most efficient, cost-effective and technicallycurrent manner.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA034196-24
Application #
7535433
Study Section
Subcommittee G - Education (NCI)
Project Start
2007-07-01
Project End
2012-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
24
Fiscal Year
2007
Total Cost
$193,999
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
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Shi, Jiayuan; Hua, Li; Harmer, Danielle et al. (2018) Cre Driver Mice Targeting Macrophages. Methods Mol Biol 1784:263-275
Hosur, Vishnu; Farley, Michelle L; Low, Benjamin E et al. (2018) RHBDF2-Regulated Growth Factor Signaling in a Rare Human Disease, Tylosis With Esophageal Cancer: What Can We Learn From Murine Models? Front Genet 9:233
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Dominguez, Pilar M; Ghamlouch, Hussein; Rosikiewicz, Wojciech et al. (2018) TET2 Deficiency Causes Germinal Center Hyperplasia, Impairs Plasma Cell Differentiation, and Promotes B-cell Lymphomagenesis. Cancer Discov 8:1632-1653
Paigen, Kenneth; Petkov, Petko M (2018) PRDM9 and Its Role in Genetic Recombination. Trends Genet 34:291-300
Schloss, Jennifer; Ali, Riyasat; Racine, Jeremy J et al. (2018) HLA-B*39:06 Efficiently Mediates Type 1 Diabetes in a Mouse Model Incorporating Reduced Thymic Insulin Expression. J Immunol 200:3353-3363
Nakatsuji, Teruaki; Chen, Tiffany H; Butcher, Anna M et al. (2018) A commensal strain of Staphylococcus epidermidis protects against skin neoplasia. Sci Adv 4:eaao4502
Racine, Jeremy J; Stewart, Isabel; Ratiu, Jeremy et al. (2018) Improved Murine MHC-Deficient HLA Transgenic NOD Mouse Models for Type 1 Diabetes Therapy Development. Diabetes 67:923-935
Ye, Fengdan; Jia, Dongya; Lu, Mingyang et al. (2018) Modularity of the metabolic gene network as a prognostic biomarker for hepatocellular carcinoma. Oncotarget 9:15015-15026

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