| Director
|
Facility
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Daniel C. Marcus, DSc
Program Director
Lisa Duer
Grant Manager
Brian
Willis
Administrative Assistant |
Administrative Core |

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Philine Wangemann,
PhD Director, Core B
Joel
Sanneman Confocal Core Manager
| Confocal Microfluorometry and
Microscopy |

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Philine Wangemann,
PhD Co-Director, Core C
Roman R. Ganta, PhD
Co-Director, Core C
Nithya Raveendran Core Manager, Molecular Biology
and Biochemistry Support Facility
|
Molecular Biology and Biochemistry Support Facility |
 |
Daniel C. Marcus, DSc
Director, Core D |
Epithelial Electrophysiology |
COBRE Administrative Office
Core A supports the establishment and maintenance
of the COBRE Administrative Office. The Administrative Core is headed
by the PI, Dr. Daniel C. Marcus, assisted by the Manager/Administrator,
Lisa Duer. This core organizes and supports the formal mentoring
meetings, the External Speaker Seminar Series, the Literature Review
Series and meetings of both the External Advisory Committee and the
Internal Advisory Committee. The PI travels to NCRR in Bethesda MD
each year to confer with NCRR staff. The Advisory Committees will consider
applications for funding from additional junior investigators at the
participating universities and for common-use equipment or facilities
after graduation of the initial junior investigators from the COBRE.
Confocal Microfluorometry and
Microscopy
Core B, the
Confocal Microfluorometry and
Microscopy Core
facility provides instrumentation, expertise, training and mentoring in confocal microfluorometry and microscopy necessary for the advancement of
COBRE research projects. Projects depend critically on microfluorometry of
fast Ca2+ signals in cultured and native epithelial tissues, on the subcellular visualization of molecules including the 3-dimensional
reconstruction of labeling, on co-localization experiments, where maximal
resolution and color separation through emission fingerprinting are
necessary and on advanced co-localization techniques such as FRET, for
which emission scanning is critical. Instrumentation, expertise, training
and mentoring will enable COBRE investigators to establish themselves
through advancing their research on epithelia in health and disease.
Molecular Biology and Biochemistry Support Facility
Core C supports the
establishment and maintenance of the COBRE Molecular Biology Support
Facility. The Core provides: a)
the interface, expertise, training and mentoring in gene array analysis
necessary for the advancement of COBRE projects on different epithelia, b)
equipment and support for measurement and analysis of RNA quantity &
quality, c)
equipment and support for quantitative, real time PCR and d) equipment and
support for DNA sequencing. All projects will benefit from support by this
Core facility. This facility enables COBRE investigators to establish
themselves through advancing their research on epithelia in health and
disease.
Epithelial Electrophysiology
Core D supports the establishment and maintenance
of the COBRE Epithelial Electrophysiology Core facility. The Core
provides the instrumentation, expertise, training and mentoring in
epithelial electrophysiology necessary to advance COBRE
projects on different epithelia. These projects
depend critically on making non-invasive current and non-radioactive ion
flux measurements. Based on our expertise and experience, and with the goal
to advance the mentored projects, we have identified the following
equipment for this facility: 1) vibrating current-density probe, 2)
self-referencing ion-selective electrodes and 3) scanning conductance
probe. This instrumentation, in conjunction with the provided expertise,
training and mentoring enables COBRE investigators to establish
themselves through advancing their research on epithelia in health and
disease.
We request that all Core Facility users
include a statement of acknowledgement in their research publications. A
sample statement would be:
We acknowledge the Kansas State University
COBRE [Confocal Microscopy Facility] [Molecular Biology Support Core]
[Epithelial Electrophysiology Facility] supported by NIH grant
P20-RR017686.
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