The Fluorescence-Activated Cell Sorting (FACS) Facility has provided flow cytometry services to AECCC investigators since 1980. This shared resource makes available instrumentation for fluorescence analysis of cell surface and cytoplasmic markers, DNA content, apoptosis, changes in intracellular calcium concentration and for multiparameter cell sorting. The facility also offers computer support for analysis of flow cytometric data and advice on the design and implementation of experimental protocols. At the time of the last CCSG review, the facility was equipped with a FACscan analytic flow cytometer, a FACStar Plus Cell Sorter, and a Zeiss fluorescence microscope. During the current grant period the facility has acquired a second analyzer, the FACS Calibur, and an AutoMACS magnetic cell sorter. A Zeiss inverted fluorescence microscope has also been acquired and a high speed FACS Vantage cell sorter has recently been leased and will be installed shortly. These changes in instrumentation permit the facility to offer analysis of cellular apoptosis, using annexin staining, the TUNEL assay and measurement of DNA content and activation assays that monitor fluxes in intracellular calcium concentration. In addition, the new high speed cell sorter will provide simultaneous analysis of cell populations using up to six fluors and eight parameters simultaneously. The Director of the Facility carries out cell sorting and trains and supervises AECCC investigators, students, fellows, technicians and faculty in the operation of the analyzers and the AutoMACS. The Director maintains the instruments, provides instruction and ensures quality control. This facility is essential for the phenotypic analysis of normal and malignant lymphoid and other cells and for the monitoring of changes in protein expression that accompany activation and transformation of cells of diverse lineages. The high cost of the instrumentation and the need for skilled personnel mandates the availability of a shared resource for flow cytometry. The facility also permits maximum and efficient utilization of the instrumentation. This shared resource represents the only access to flow cytometry and cell sorting within the institution and thus is crucial to AECCC investigators.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013330-30
Application #
6502388
Study Section
Project Start
1977-06-01
Project End
2006-06-30
Budget Start
Budget End
Support Year
30
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Zamurrad, Sumaira; Hatch, Hayden A M; Drelon, Coralie et al. (2018) A Drosophila Model of Intellectual Disability Caused by Mutations in the Histone Demethylase KDM5. Cell Rep 22:2359-2369
Sparano, Joseph A (2018) Prognostic gene expression assays in breast cancer: are two better than one? NPJ Breast Cancer 4:11
Centini, Ryan; Tsang, Mark; Iwata, Terri et al. (2018) Loss of Fnip1 alters kidney developmental transcriptional program and synergizes with TSC1 loss to promote mTORC1 activation and renal cyst formation. PLoS One 13:e0197973
Nadaradjane, Celine; Yang, Chia-Ping Huang; Rodriguez-Gabin, Alicia et al. (2018) Improved Dose-Response Relationship of (+)-Discodermolide-Taxol Hybrid Congeners. J Nat Prod 81:607-615
Tiwari, Sangeeta; van Tonder, Andries J; Vilchèze, Catherine et al. (2018) Arginine-deprivation-induced oxidative damage sterilizes Mycobacterium tuberculosis. Proc Natl Acad Sci U S A 115:9779-9784
Celestrin, Kevin; Díaz-Balzac, Carlos A; Tang, Leo T H et al. (2018) Four specific immunoglobulin domains in UNC-52/Perlecan function with NID-1/Nidogen during dendrite morphogenesis in Caenorhabditis elegans. Development 145:
Haider, Afreen; Wei, Yu-Chen; Lim, Koini et al. (2018) PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress. Dev Cell 45:481-495.e8
Cai, Ying; Lin, Jhih-Rong; Zhang, Quanwei et al. (2018) Epigenetic alterations to Polycomb targets precede malignant transition in a mouse model of breast cancer. Sci Rep 8:5535
Li, Ke; Baker, Nicholas E (2018) Regulation of the Drosophila ID protein Extra macrochaetae by proneural dimerization partners. Elife 7:
Xie, Xianhong; Xue, Xiaonan; Strickler, Howard D (2018) Generalized linear mixed model for binary outcomes when covariates are subject to measurement errors and detection limits. Stat Med 37:119-136

Showing the most recent 10 out of 1508 publications