The Cell Biology & Microinjection Service provides researchers with valuable tools for studies of gene expression in vivo and a mechanism for creating induced mutations. The Service provides the expertise and supplies necessary for embryonic stem cell (ES cell) culture and manipulation, ES cell aggregation, and both blastocyst and pronuclear injection for the creation of targeted mutant and transgenic mice, which can be produced on both inbred and hybrid genetic backgrounds. C57BL/6J, 129/ImJ and a host of hybrid 129 ES cell lines have been derived and tested by the Service?s staff, and are available for use. In addition, the highly skilled technical staff perform technically challenging protocols such as pronuclear injection of very large (>200kb) BAC clones. Service is provided to Cancer Center staff at the level required; investigators can forward manipulated ES cells to the Service for microinjection and chimera production, or they may opt to forward DNA constructs for electroporation, ES cell cloning, screening, and microinjection. Related services and reagents are available including pathogen-free timed pregnancies, superovulated and vasectomized mice, premeasured and tested hormones, feeder cells, and cell culture supplies. The Service assists in the breeding of founder and chimeric mice, complete ovarian transplants, and timed harvesting of eggs. Cell Biology & Microinjection has been supported by Cancer Center support grant (CCSG) funds for the past five years, during which time use of the Service has increased an average of 33.7 percent. Thomas Gridley, Ph.D., a developmental biologist, has served as the Scientific Staff Supervisor since 1999. Dr. Gridley communicates regularly with the User Group and service personnel to insure that users have equitable service access and that their needs are met in the most efficient, cost effective and technically current manner. Service's staff work closely with Microchemistry Service staff to provide comprehensive tools and capabilities to Cancer Center staff for state-of-the-art genetic engineering.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA034196-20
Application #
6652228
Study Section
Project Start
2002-08-01
Project End
2003-07-31
Budget Start
Budget End
Support Year
20
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
Becker, Timothy; Lee, Wan-Ping; Leone, Joseph et al. (2018) FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods. Genome Biol 19:38
Wang, Qianghu; Hu, Baoli; Hu, Xin et al. (2018) Tumor Evolution of Glioma-Intrinsic Gene Expression Subtypes Associates with Immunological Changes in the Microenvironment. Cancer Cell 33:152
Richter, Wolfgang F; Christianson, Gregory J; Frances, Nicolas et al. (2018) Hematopoietic cells as site of first-pass catabolism after subcutaneous dosing and contributors to systemic clearance of a monoclonal antibody in mice. MAbs 10:803-813
Tamura, Ryo; Yoshihara, Kosuke; Saito, Tetsuya et al. (2018) Novel therapeutic strategy for cervical cancer harboring FGFR3-TACC3 fusions. Oncogenesis 7:4
Rutherford, Sarah C; Fachel, Angela A; Li, Sheng et al. (2018) Extracellular vesicles in DLBCL provide abundant clues to aberrant transcriptional programming and genomic alterations. Blood 132:e13-e23
Barthel, Floris P; Wesseling, Pieter; Verhaak, Roel G W (2018) Reconstructing the molecular life history of gliomas. Acta Neuropathol 135:649-670
Kim, Hyunsoo; Kumar, Pooja; Menghi, Francesca et al. (2018) High-resolution deconstruction of evolution induced by chemotherapy treatments in breast cancer xenografts. Sci Rep 8:17937
Winer, Benjamin Y; Shirvani-Dastgerdi, Elham; Bram, Yaron et al. (2018) Preclinical assessment of antiviral combination therapy in a genetically humanized mouse model for hepatitis delta virus infection. Sci Transl Med 10:
Barthel, Floris P; Johnson, Kevin C; Wesseling, Pieter et al. (2018) Evolving Insights into the Molecular Neuropathology of Diffuse Gliomas in Adults. Neurol Clin 36:421-437
Schechter, Lisa M; Creely, David P; Garner, Cherilyn D et al. (2018) Extensive Gene Amplification as a Mechanism for Piperacillin-Tazobactam Resistance in Escherichia coli. MBio 9:

Showing the most recent 10 out of 1156 publications