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COMMERCE BUSINESS DAILY ISSUE OF JULY 12,1999 PSA#2385NASA/George C. Marshall Space Flight Center, Procurement Office,
Marshall Space Flight Center, AL 35812 66 -- PROTEIN PURIFICATION SYSTEM SOL 8-1-9-10-C3280 DUE 073099 POC
Glen A. Alexander, Contract Specialist, Phone (256) 544-3797, Fax (256)
544-9354, Email glen.alexander@msfc.nasa.gov -- Valerie N. Holmes,
Contracting Officer, Phone (256)544-0314, Fax (256)544-9354, Email
valerie.holmes@msfc.nasa.gov WEB: Click here for the latest information
about this notice,
http://nais.nasa.gov/EPS/MSFC/date.html#8-1-9-10-C3280. E-MAIL: Glen A.
Alexander, glen.alexander@msfc.nasa.gov. This notice is a combined
synopsis/solicitation for commercial items prepared in accordance with
the format in FAR Subpart 12.6, as supplemented with additional
information included in this notice. This announcement constitutes the
only solicitation; quotes are being requested and a written
solicitation will not be issued. This procurement is being conducted
under the Simplified Acquisition Procedures (SAP). We require the
ability to purify biomolecules from complex starting materials derived
from cell lysates, tissue homogenates, recombinant protein expression
systems and other sources. The system we will purchase must be able to
perform separations based on a variety of sample characteristics, such
as molecular weight, net surface charge, and hydrophobicity, while
retaining biological activity. We may want to automate the running of
large open columns on the system, as well as a variety of gel
filtration media. We require a flow rate range of .01-100 ml/min at
pressures ranging from 0-1500 psi. The system must have the capability
of interchanging pump heads as a future option. Because the resolution
we require may necessitate the use of very precise, shallow gradients,
the system must be a two-pump gradient system, with dynamic mixing, as
evidence suggests that this configuration produces the highest accuracy
and precision in gradient formation. Because we will be using salt
buffers, the entire wetted flow path of the system must be inert to
halides. The controller must allow programs to be time-based,
volume-based, or column-volume based. In order to facilitate cleaning,
storage, and selection of our various chromatographic columns, the
system must include two motorized valves, one for the column inlets and
one for the column outlets. This is also necessary so that the desired
column may be selected without removing the tubing and fittings by
which the column is plumbed into the flow path, since such removal of
fittings risks introduction of air into the column. The system
controller must allow the userto be entering details of the next
purification at the same time the current separation is being done, or
to simultaneously be integrating and evaluating the results of earlier
runs. If desired the user must be able to leave the controlling program
and enter into word processing, spreadsheets, etc. that lie outside the
operating program. Control of up to four motorized valves, chart
recorder, fraction collector, dynamic gradient mixer, and two pumps
must all be possible from the system controller. The pumps, UV and
Conductivity monitors, valves, and fraction collector must all be
specified for use in a cold room at 4 degrees C. The controller must
accept seven input signals (e.g. 3 UV wavelengths, conductivity, pH,
temperature, pressure). It must be capable of plotting, and integrating
these signals, as well as using them to trigger sub-routines in the
programming when the signal exceeds a preset threshold, to allow the
automation of multi-dimensional separations. The system must include
one automatic three-position injection valve (load, inject, wash
positions), which will allow for automated sample loading . The system
controller should allow for the automation of the optimization of
separation parameters (e.g. sample volume, flow rate, gradient slope,
buffer pH ). This should allow a small amount of sample to be consumed
in optimization of the purification scheme, after which the best
regime can be scaled up on the same LC system. Column equilibration
before and after sample injection and elution must be capable of being
monitored, with a feed-back loop to the control system, so we can be
certain equilibration is completed without consuming excess volume of
sometimes expensive buffers. The documentation of each run should be
automatic and exhaustive, so that for purposes of subsequent
replication and eventual publication, no detail is left unrecorded.
Post-run chromatographic analysis and reporting functions should also
be included. In order to protect our columns, the system must have a
settable pressure limit system, which will stop the pump and generate
an audible and visual warning in the event pressure exceeds the preset
limit. We also require that the controller allow the user the option
of including in his/her chromatographic methods, commands which will
automatically reduce the flow rate if an over-pressurization occurs as
sample is being applied or eluted from the column. Additional
variables which should also be programmable to trigger sub-routines
(e.g. new tube on fraction collector; valve changes; etc.) should
include UV or conductivity signals. The controller should permit
automatic running of up to 32 different chromatographic programs in a
user-designated sequence, changing any single or several variables of
choice. It must turn off the pump flow when a signal is received from
the fraction collector indicating there no tubes remaining, so that
valuable sample is preserved. The system must automatically and
continuously record throughout each chromatographic run the following
parameters: flow rate,auto-scaled UV signal (which can also be set to
a defined range by the user if desired, with all data still being
collected), actual and programmed conductivity of the eluent, eluent pH
(with both ion concentration and temperature being accounted for),
system pressure, accumulated time and volume of the run, all valve
positions and changes in position, and activity of a fraction
collector. It must allow these recorded data to be called up later for
interpretation and to aid in future replication of results. It must
also allow for post-run analysis of chromatograms, export data to other
spreadsheet programs, and generate custom written reports. The system
must have the ability to be interfaced with an autosampler and be
controlled from the system software. The system must have the ability
to perform buffer blending and do this in a manner that is based on pKa
and accounts for both ion concentration and temperature. The system
must have an eight line buffer valve that allows for cleaning in place
programs as well as automated Gel Filtration and Affinity techniques.
The evaluation software must be capable of custom reports, HETP
calculations, Sigma, Resolution and Histograms in addition to
overlaying multiple runs and performing numerous manipulations. The
software must contain template protocols for purification of synthetic
peptides, labelled synthetic oligonucleotides, native peptides, and
protein fragments in addition to templates for general chromatographic
techniques e.g. gel filtration, RPC, affinity, IEX, HIC and CIP. The
software must have on-line HELP that pertains to the all portions of
the program. The software must provide buffer preparation protocols on
line and an advisor program that has online part numbers, column and
media information and troubleshooting. The software and system must be
capable of validation by FDA standards. All data must be easily
exportable into ASCII format for importation into alternative programs
ie Excel or Word for publication and presentation. The system must
allow for manual intervention while a programmed method is running. The
systems UV detection lamp must turn on and off automatically when the
system is running saving on lamp life in addition to being
automatically calibrated every time the lamp turns on. At each start-up
each instrument must perform an automatic self-diagnostic test and
calibrate appropriate settings ensuring top performance throughout the
day-to-day operation. The system must require minimal bench space. The
system must be also mounted on a swivel base allowing accessibility to
all sides of the system. The system must allow peak fractionation
based on slope of threshold. The system must have an outlet valve
allowing for sample collection to be done with included fraction
collector or through alternate outlet valve ports for larger sample
collection. System should provide a free-standing computer with at
least the following specifications: a 350 MHz Pentium II processor,
100mHz bus speed, 512 KB cache, 6.4 GB Ultra ATA hard drive, 3.5" 1.44
floppy drive, 24X CD-ROM drive, Iomega internal ZIP100 drive (IDE
version), ATI Rage PRO Turbo AGP 2X enhanced graphics, 4MB video
SGRAM-ESS ES1869 embedded sound card, 1 AGP expansion slot, 2 ISA
expansion slots, 5 PCI expansion slots, 2 serial and 1 parallel port,
104 key enhanced keyboard, PS/2 style mouse, PCI network interface
card, 17 inch Compaq V75 monitor or equivalent, and Microsoft Windows
NT 4.0 Workstation 4.0 software and documentation. Computer should have
Standard three year limited warranty (first year on-site). Computer
must be able to perform true multi-tasking to outside applications i.e.
word processing. Installation of purification system and training must
be provided by the vendor, at no additional cost. The system quoted
should include spare parts we are likely to need during the first 12
months of operation. The system must have a 1 year warranty on all
parts and service. The provisions and clauses in the RFQ are those in
effect through FAC 99-12. This procurement is a total small business
set-aside. See Note 1. The SIC code and the small business size
standard for this procurement are 3821 and 500, respectively. The
quoter shall state in their quotation their size status for this
procurement. All qualified responsible business sources may submit a
quotation which shall be considered by the agency. Delivery to MSFC is
required within 45 days ARO. Delivery shall be FOB Destination. The
DPAS rating for this procurement is DO-C9. Quotations for the items(s)
described above are due by Close of Business, July 30, 1999, and may
be mailed or faxed to the identified point of contact by the date/time
specified and include, solicitation number, FOB destination to this
Center, proposed delivery schedule, discount/payment terms, warranty
duration (if applicable), taxpayer identification number (TIN),
identification of any special commercial terms, and be signed by an
authorized company representative. Quoters are encouraged to use the
Standard Form 1449, Solicitation/Contract/Order for Commercial Items
form found at URL: http://procure.arc.nasa.gov/Acq/Forms/Index.html to
submit a quotation. Quoters shall provide the information required by
FAR 52.212-1. Addenda to FAR 52.212-1 are as follows: MSFC 52.213-91.
If the end product(s) quoted is other than domestic end product(s) as
defined in the clause entitled "Buy American Act -- Supplies," the
quoter shall so state and shall list the country of origin. The
Representations and Certifications required by FAR 52.2l2-3 may be
obtained via the internet at URL:
http://ec.msfc.nasa.gov/msfc/pub/reps_certs/sats/ FAR 52.212-4 is
applicable. Addenda to FAR 52.212-4 are as follows: MSFC 52.232-90, NFS
1852.246-71, FAR 52.204-4, 52.211-15, and 52.247-34. FAR 52.212-5 is
applicable and the following identified clauses are incorporated by
reference: FAR 52.222-21, 52.222-26, 52.222-35, 52.222-36, 52.222-37,
and 52.225-3. Questions regarding this acquisition must be submitted in
writing no later than Close of Business July 19, 1999. Quotations are
due by COB July 30, 1999. Selection and award will be made to the
lowest priced, technically acceptable quoter. Technical acceptability
will be determined by information submitted by the quoter providing a
description in sufficient detail to show that the product quoted meets
the Government's requirement. Quoters must provide copies of the
provision at 52.212-3, Offeror Representation and Certifications --
Commercial Items with their quote. See above for where to obtain copies
of the form via the Internet. An ombudsman has been appointed -- See
Internet Note "B". It is the quoter's responsibility to monitor the
following Internet site for the release of amendments (if any):
http://procurement.nasa.gov/EPS/MSFC/class.html. Potential quoters will
be responsible for downloading their own copy of this combination
synopsis/solicitation and amendments (if any). See Note(s). Any
referenced notes can be viewed at the following URL:
http://genesis.gsfc.nasa.gov/nasanote.html Posted 07/08/99
(D-SN351924). (0189) Loren Data Corp. http://www.ld.com (SYN# 0392 19990712\66-0023.SOL)
66 - Instruments and Laboratory Equipment Index Page
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