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Flow Cytometry Service Request Form

Immunology Core Facilities

core logoFLOW CYTOMETRY REQUEST FORM

Flow Cytometry Unit of Immunology Core at
DAI 5085 and BIGGS C505
Core Director: Dr. David A. Lawrence BIGGS C539 (402-5684)
Assistants: at BIGGS -- Joan Pedersen-Lane/Renjie Song/Steve Rich
at DAI -- Kenneth Class
(Telephone: BIGGS C505 474-3697; DAI 5085 486-4915)

INFORMATION ABOUT FLOW CYTOMETERS

Becton Dickinson FACSVantage: (DAI)
Laser excitation wavelengths: two lasers generating three laser lines
Lines at 350 nm, 488 nm, 633 nm.
Eight-parameter detection: Forward scatter, Side scatter and five fluorescent dyes.
A MacroSORT option is available for large particle (up to 150um)
analysis or sorting. An Automatic Cell Deposition Unit (ACDU) That sorts a predefined number of cells into individual wells of a 96 or 24 well microtiter plate is also available. Location: DAI /5085

Becton Dickinson FACSCalibur: (DAI)
Laser excitation wavelength: Argon 488nm and red diode 635 nm
Emission wavelength detection: Forward scatter (size), side scatter (granularity), Four high performance, high dynamic range photomultipliers with band pass filters: 530nm (FITC), 585 nm (PE/PI), 661nm (APC), and 650 nm (PerCP) with FL3 or >670nm with FL4.
FACSLoader provides automated or manual introduction of prepared samples, featuring removable 40-tube carousels, with on-board mixing.

Becton Dickinson FACScan: (DAI & BIGGS)
Laser excitation wavelength: Argon 488nm
Emission wavelength detection: up to 5 parameters; forward scatter (size), side scatter (granularity), FL1: 515-545nm(green), FL 2: 564-606nm(yellow/orange), FL3 >650nm(red).

INFORMATION PROVIDED BY INVESTIGATOR: (please print).

NAME:


PRINCIPAL INVESTIGATOR:


LAB ROOM # ____________    PHONE # __________________________

FUNDING INFORMATION: REQUIRED BEFORE USAGE
HRI ACCOUNT#__________________________STATE ACCOUNT#__________________
Please contact core personnel about the charge fee for flow usage.
PI will be billed quarterly.

Sample Preparation Requirements:
SINGLE PARTICLES in a NON-PROTEIN BUFFER
Concentration of 0.5-2.0 x 106 particles/ mL.
Volume at 0.5-1 mL/sample/tube.
For new protocols: All appropriate controls necessary for parameter setups must be included as determined by Core personnel.

SAMPLE INFORMATION: please be as detailed as possible, attach additional pages as necessary.

FLUORSCENT PROBE/DYE CHARACTERISTICS (spectra, Ex nm, Em nm)
_______________________________________________

DESCRIPTION OF SAMPLE: (cells including their source, DNA, and relative size)
_______________________________________________

DESCRIPTION OF SAMPLE PROTOCOL, GOALS AND REFERENCE:
_________________________________________
_________________________________________
_________________________________________
_________________________________________
_________________________________________

APPROVED BY (ALL SIGNATURES ARE REQUIRED BEFORE USAGE)
PI: _________________________________________ DATE: _________
LAB CHIEF: _________________________________DATE: _________
CORE DIRECTOR: __________________________ DATE: _________

Print & Send completed form to:
Flow Unit Assistants: Joan Pedersen-Lane/Renjie Song/Steve Rich, (DAI) Kenneth Class
BIGGS C505 474-3697, DAI 5085 486- 4915
Or to Core Director, Dr. David Lawrence BIGGS, C539. Phone 402-5684; Fax 474-1412