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COMMERCE BUSINESS DAILY ISSUE OF FEBRUARY 10,1999 PSA#2280U.S. Department of Agriculture, ARS, LPSI, East Side Service Center,
Bldg. 307, Room 129, BARC-East, Beltsville, MD 20705 66 -- CUSTOM NORMALIZATION CDNA LIBRARY SOL 3K45-JW-004 DUE 022599 POC
John Wilkinson, Telephone (301) 504-5799, Fax (301) 504-8696 USDA
intends to award the following solicitation as a sole source
procurement due to the "PATENT" that "Life Technologies Inc." holds for
the "Superscript RT Enzyme". USDA intends to purchase a "Custom
normalized cDNA library". This procurement request is for cDNA library
normalization service to construct a normalized cDNA library from
bovine mammary gland tissue. A normalized cDNA library of low clonal
redundancy is required as a resource by our laboratory to efficiently
generate 10,000 unique expressed sequence tags (ESTs) from the bovine
mammary gland. This service needs to follow specific parameters to
insure our lab obtains the highest quality cDNA library necessary for
our EST project. First, mRNA has to be isolated from seven unique
mammary tissue samples. The mRNA must be mixed in equimolar
concentrations before producing >1 kb cDNA fragments with a high
fidelity enzyme like SuperScript II H- RNase reverse transcriptase. We
require these cDNAs fragments be cloned into pCMV Sport 6.0 vectorand
transformed into DH10B cells. From these reactions, two libraries
should be produced; each with >1 x 107 primary clones. Individual
clones from these libraries need to be analyzed to determined average
cDNA insert size. The primary libraries have to be produced in 4-6
weeks. A hundred clones are then returned to our laboratory for
sequence analysis to determine redundant clones for quality control
analysis of the normalization procedure. The primary libraries are
amplified using a semi-solid agarose procedure to minimize clonal bias
that would occur in a liquid amplification. The libraries should be
amplified 10-100,000 fold. Once amplified, the DNA isolated from the
libraries should undergo a Cot-500 normalization using subtractive
hybridization technology. The DNA is again transformed into E. coli to
produce a final copy of the normalized cDNA library containing a
minimum of 5 x 106 unique clones with an average insert size >1 kb.
Completion of the normalized library from the primary libraries has to
be done in 4-6 weeks. The resultant normalized library should have
reduced abundant genes by 10-100 fold. Levels of ribosomal RNA clones
also need to be determined by colony hybridization. All steps used to
produce this cDNA library must be assured by a quality control process.
All residual materials need to be returned to our laboratory. A copy of
the solicitation will be made by WRITTEN REQUEST ONLY. This
solicitation incorporates clauses that are in effect through Federal
Acquisition 97-7. This acquisition will be solicited on a unrestricted
basis. The Standard Industrial Classification Code is 8731. Delivery
is required 30 days after award of this solicitation. Delivery shall be
F.O.B. Destination to the U.S. Department of Agriculture in Beltsville,
Maryland. Any interested/qualified sources who can provide the item
stated above, must respond by February 28, 1999. All responses will be
evaluated in order to determine the capabilities stated in the RFQ.
The Government will award a contract resulting from this solicitation
to the responsive/responsible offeror whose quote conforms to the
solicitation and will be most advantageous to the Government based on
price. Posted 02/08/99 (W-SN296138). (0039) Loren Data Corp. http://www.ld.com (SYN# 0181 19990210\66-0003.SOL)
66 - Instruments and Laboratory Equipment Index Page
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