MGH RESEARCH CORES

Nucleic Acid Quantitation
Biostatistics Core
Clinical Genetic Research Facility
Clinical Research Program
DNA Microarray Core (Seed)
DNA Sequencing Core
DNA Synthesis Core
Electrophysiology Core
Flow Cytometry Core
Glass Washing and Autoclaving Core
Knight Surgical Research Laboratory
Knockout Facility
Laser Capture Microscopy Core
Magnetic Resonance Imaging Core
Microscopy and Image Analysis Core
Microscopy Core (Brown)
Model Shop (Prototyping and Fabrication Facility)
Morphometry Analysis Center
Musculoskeletal Imaging Research Core
Neuroscience Microscope Core
Nucleic Acid Quantitation (Real-Time PCR) Core
Peptide Synthesis/Protein Sequencing Core
PET Core
Radiation Safety Core
Transgenic Core
Transgenic Drosophila Fly Core
Tumor Imaging Metrics Core
Vector Development and Production Core
Web Development Core
 

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Nucleic Acid Quantitation Core (Real-Time PCR)
Director: Samuel Rabkin
Location: Building 149 13th Street, Room 6029, Charlestown
 

Core Summary:

The Nucleic Acide Quantification Core (Real-Time PCR) offers quantitative measurement of DNA or RNA levels using real-time PCR.

Personnel/Contact Information:

Director: Samuel Rabkin, Ph.D.
Phone: (617) 726-6817
Fax: (617) 643-3422
Email: rabkin@helix.mgh.harvard.edu

Other Staff:

Research Technician: Luba Zagachin
Phone: (617) 726-9587
Fax: (617) 726-7864
Email: lzagachin@partners.org

Facilities and Equipment:

Location of Core:

The facility is located at Building 149 13th Street, Room 6029, Charlestown.

Major Equipment:

Real-time quantitative PCR machine (ABI Prism 7000 Sequence Detector System)
Software for primer selection and data analysis
Automated nucleic acid purification and processing (ABI Prism 6100 Nucleic Acid PrepStation)

Services:

Real-time quantitative PCR provides improved sensitivity, accuracy, speed, and throughput
over standard PCR methods. The ABI Prism 7000 is a new instrument that replaces the
ABI 7700, which has been a standard for real-time PCR. It has a detection range of over 5 logs in a 96 well format. Detection is based on TaqMan fluorescent probes with 5' reporter and 3' quencher labels, such that synthesis from flanking primers leads to cleavage of the 5' reporter dye and detectable fluorescence. TaqMan probes can be synthesized with different color dyes permitting the analysis of multiple sequences in a single PCR reaction, so that each reaction can contain an internal control. The TaqMan probes can also be used for allelic discrimination assays. SYBR green can be used in place of the TaqMan probes to detect total PCR product.

Fee Schedule/Rates:

Service
MGH
Laser Capture Microscopy
$50/hour

Getting Started:

To access the core, please contact Luba Zagachin at (617) 726-9587 or by email at
lzagachin@partners.org.

Departmental Web Link:

http://www.massgeneral.org/ncs/neuro_core_NucleicAcidQuantitation.htm