title: UofToronto-yeastORF-6.4k3.48

status: Public on Feb 28 2006

city: Boston

first: Pamela

middle: A

last: Silver

state: MA

address: 200 Longwood Ave

department: Systems Biology

country: USA

institute: Harvard Medical School

organism: Saccharomyces cerevisiae

technology: spotted DNA/cDNA

distribution: non-commercial

manufacture_protocol: Double-spotted array containing 6,240 yeast ORFs (plus control spots totalling 6.4K).


title: UofToronto-yeastORF-6.4k6


title: CodeLink Uniset Mouse I Bioarray

status: Public on Feb 20 2006

city: Houston

first: Huiping

last: Zhu

state: TX

address: 2121 W. Holcombe Blvd

department: Center for Environmental and Genetic Medicine

institute: Institute of Biosciences and Technology, TAMUSHSC

organism: Mus musculus

technology: spotted oligonucleotide

distribution: custom-commercial


title: Transcriptome analysis of a cnidarian/dinoflagellate symbiosis

status: Public on Feb 21 2006

city: Corvallis

first: Mauricio

last: Rodriguez-Lanetty

state: OR

address: 3029 Cordley Hall

department: Zoology

institute: Oregon State University

organism: Anthopleura elegantissima

description: Array slide: Ultragap (Corning)

manufacturer: Center for Genome Research and Biocomputing, Oregon State University

first: Wendy

middle: S

last: Phillips

first: Virginia

middle: M

last: Weis

manufacture_protocol: ArrayerSoftware:TAS Application Suite/ Arrayer:MicroGrid II/ Spotting buffer 3X SSC plus 1.5 M Betaine/


title: OMRF Microarray Core Facility Human 22k Print 13

status: Public on Feb 18 2006

city: Oklahoma City

first: Parima

last: Pathipvanich

state: OK

address: 755 Research Parkway, Suite 464

department: Arthritis/Immunology

institute: Oklahoma Medical Research Foundation

organism: Homo sapiens

description: Average feature diameter is 110 microns.

first: Mark

middle: B

last: Frank

first: Craig

last: Cadwell

first: Sean

last: Turner

first: Michael

last: Centola

manufacture_protocol: Resuspend Operon Human Version 2.1 Genome Set (Oligos, 70 mers) in 3X SSC. Print oligos with GeneMachines OmniGrid 100 at 60% humidity using Telechem Stealth 2.5 pins. UV crosslink with 300 mJ.


title: ENCODE NimbleGen hg17 tiling array

city: Calgary

last: Bieda

state: AB

address: 3330 Hospital Dr NW

department: Biochemistry and Molecular Biology

country: Canada

institute: University of Calgary

technology: in situ oligonucleotide

middle: C

manufacture_protocol:
oligos synthesized on array
Standard ENCODE hg17 array from NimbleGen


title: MPIIB Helicobacter pylori cDNA array

status: Public on Feb 23 2006

city: Berlin

first: Hans-Joachim

last: Mollenkopf

address: Charitéplatz 1

country: Germany

institute: Max-Planck-Institute for Infection Biology

organism: Helicobacter pylori

first: Dagmar

last: Beier

last: Pflock

manufacture_protocol: A whole-genome microarray containing 1649 PCR products generated with specific primer pairs derived from the genome sequences of H. pylori 26695 and J99 which were spotted in duplicate. Microarrays were produced as described previously (Gressmann, H., B. Linz, R. Ghai, K.-P. Pleissner, R. Schlapbach, Y. Yamaoka, C. Kraft, S. Suerbaum, T. F. Meyer, and M. Achtmann. 2005. Gain and loss of multiple genes during the evolution of Helicobacter pylori. PLoS Genet 1(4):e43.17).


title: Neospora 60mer Oligonucleotide Microarray

city: Beltsville

first: Robert

middle: W

last: Li

state: MD

address: Barc East

department: Animal & Natural Resources Institute

institute: USDA

organism: Neospora caninum

description:
More contact info: Dr. Wenbin Tuo
wtuo@anri.barc.usda.gov
Phone: 301-504-8258
Fax: 301-504-5306

first: Wenbin

last: Tuo

manufacture_protocol: in situ synthesis


title: INRS Homo sapiens 6649_01

status: Public on Feb 16 2006

city: Nancy

first: Bertrand

last: Rihn

address: 5 rue A Lebrun

department: Faculté de Pharmacie

country: France

institute: Université de Lorraine

first: Steve

last: Mohr

first: Philippe

last: Moncuquet

manufacture_protocol: spotted cDNA amplified by PCR on an array containing 6356 probes with sequence complementary to 4311 human genes and 2045 human ESTs


title: YALE/NIMBLEGEN_HUMAN-CHR22_372K_v1.0

city: New Haven

first: Jan

middle: Oliver

last: Korbel

state: CT

address: 266 Whitney Avenue

institute: Yale University

first: Alexander

middle: E

last: Urban

middle: O

first: Rebecca

last: Selzer

first: Sherman

last: Weissman

first: April

last: Hacker

first: Beverly

last: Emanuel

first: Joseph

middle: F

last: Cubells

first: Todd

last: Richmond

first: Roland

last: Green

first: George

middle: V

last: Popescu

last: Gerstein

last: Snyder

manufacture_protocol:
Maskless array synthesis [1] was used to construct isothermal arrays. This array contains oligonucleotides that start every 85 bp and tiles the entire nonrepetitive part of human chromosome 22 (human genome build NCBI35/hg17 was utilized).  Repetitive elements were identified using RepeatMasker [2] and oligonucleotide probes were designed to represent the nonrepetitive DNA sequence. The oligonucleotides were designed to be of variable length, adjusted to match a target melting temperature of 76°C according to the following formula: Tm = 81.5 + 16.6*(log10([Na+])) + 0.41*(%GC) - 600/length. Probe lengths were constrained to be a minimum of 45 bp and maximum of 85 bp.

[1] Nuwaysir, E.F., Huang, W., Albert, T. J., Singh, J., Nuwaysir, K., Pitas, A., Richmond, T., Gorski, T., Berg, J. P., Ballin, J. et al., Genome Res., 2002. 12: p. 1749-1755, PMID: 12421762, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=search&term=12421762

[2] Smit, A.F.A., Hubley, R. & Green, P., RepeatMasker Open-3.0, 1996-2004.


title: Bos Taurus Expression Array for Smooth Muscle Gene Expression

first: Marc

middle: E.

last: Lenburg

address: 715 Albany Street, E613B

department: Genetics and Genomics

institute: Boston University School of Medicine

organism: Bos taurus

first: Jeannette

last: Kanefsky

first: Chi-Ming

last: Hai

manufacture_protocol:
Oligonucleotide Design:  50 mer oligonucleotides for 402 experimental genes related to smooth muscle function and 78 “house-keeping” genes were by first identifying 50bp sequences within the target cDNA sequence that were unique within the Bos taurus BTGI genome database (searches performed between January and February, 2004) and then filtering these to minimize predicted RNA secondary structure and to select sequences with a predicted annealing temperature of 84 +/- 6 degrees Celsius.  These steps were performed with the program ArrayOligoSelector (Bozdech Z, Zhu J, Joachimiak MP, Cohen FE, Pulliam B, DeRisi JL.  Expression profiling of the schizont and trophozoite stages of Plasmodium falciparum with a long-oligonucleotide microarray.  Genome Biology 2003; 4:R9.).  Among the five best candidate-probe sequences, the probe that hybridized to the most 3’ region of the target was selected.  For 54 genes that we wished to include on the microarray, an orthologous Bos taurus sequence had not been identified.  For these genes we searched the Bos taurus BTGI genome database for the most homologous sequence and used this in the probe selection process.

Oligonucleotide Synthesis:  Oligonucleotides were synthesized on an ABI 3900 DNA Synthesizer (Applied Biosystems; Foster City, CA) on a 200 nmol scale using standard phorphoramidite chemistry. The 5’-DMT final group was retained for purification. All sequences were synthesized on 5’-DMT-mdC(TEG-FMOC) columns (Biosearch Technologies; Novato, CA) to provide an amino group for coupling to the array surface. Following synthesis, oligonucleotides were cleaved from the support and deprotected in conc. NH4OH at 65 °C for 5hr. The oligonucleotides were purified on Varian TOP columns (Varian Instruments; Walnut Creek, CA) following the manufacturer’s protocol. Quantitation was performed on a Wallac 1420 Victor¬2 plate reader (Perkin Elmer Life Sciences; Boston, MA) using an Oligreen ssDNA Quantitation Kit (Molecular Probes; Eugene, OR).

Array Preparation: Oligonucleotides were aliquoted into 384-well spotting plates to produce a final concentration of 50 μM in 150 mM sodium phosphate pH 8.5. In addition to the gene specific oligonucleotides, the spotting plates contain SpotReport Alien Oligo sequences (Stratagene; La Jolla, CA) for use in balancing the intensities of the two signal channels and solvent blanks. Spotting was performed on a QArraymini (Genetix; Boston, MA) employing Stelth SMP4 pins (Telechem; Sunnyvale, CA). Oligonucleotides were spotted in duplicate onto Codelink slides (Amersham Biosciences; Piscataway, NJ) at 25 °C and 55% relative humidity, with the spotting plates chilled to 15 °C. Following spotting, the arrays were incubated for 24 hrs in a sealed container containing a NaCl slurry (~75% relative humidity). The arrays were washed, with agitation on a shaker, in 4X SSC; 0.1% SDS at 50 °C for 30 min, rinsed twice with water, and dried by centrifugation at 900 rpm for 10 min.


title: Buck Institute Human 8k cDNA microarray

status: Public on Feb 17 2006

city: Ottawa

first: Douglas

middle: Joseph

last: Mahoney

state: ON

address: 401 Smyth Rd

department: Apoptosis Research Center

institute: CHEO Research Institute

manufacturer: Genomics Facility, Buck Institute for Age Research

middle: J

first: Gianni

last: Parise

first: Simon

last: Melov

first: Adeel

last: Safdar

first: Mark

last: Tarnopolsky

manufacture_protocol: 8,432 randomly chosen cDNAs from a 40k Research Genetics human cDNA library were amplified under standard conditions (GeneAmp PCR System 9700) with the help of a volumetric robot (Tecan/Genesis, RSP150 and Tomtec/Quadra 384).  Amplified products were transferred to a 384-well plates, purified transferred to 384-well print plates (Genetix), dried and resuspended in print buffer (3xSSC, 1.5M Betaine).  Spotted cDNA microarrays were generated on glass slides (MWC epoxy) using an Omnigene (GeneMachines) microarrayer.  After printing, slides were incubated overnight at 50% humidity, UV irradiated (65 ujoules), and stored in a desicator until hybridization.


title: WRAIR Homo sapiens 6.7k expression in SHIV-positive Rhesus

status: Public on Feb 26 2006

city: Silver Spring

first: Rasha

last: Hammamieh

address: 503 Robert Grant Ave

department: Molecular Pathology

institute: Walter Reed Army Institute of Research

first: R

first: M

last: Jett

first: N

last: Chakraborty

first: E

last: Carroll

first: A

last: Phillips

manufacture_protocol: Custom array


title: HMS Macaca mulatta 2.7K V1.0

status: Public on Feb 27 2006

first: Andrei

last: Tkatchenko

address: 220 Longwood Avenue, B2-201

department: Neurobiology

organism: Macaca mulatta

manufacturer: Dept. of Genetics, Harvard Medical School

first: Pamela

last: Walsh

first: Tatiana

first: Stefano

last: Gustincich

first: Elio

last: Raviola

manufacture_protocol:
cDNA subtractions and construction of cDNA libraries were performed as previously described. Briefly, subtracted cDNA libraries were generated using the PCR-Select cDNA Subtraction Kit (BD
Biosciences Clontech, Mountain View, CA) by cloning the secondary PCR
products into the pCRII-TOPO vector (Invitrogen, Carlsbad, CA). Two subtractions were carried out resulting in two cDNA libraries. One library was
enriched in clones potentially up-regulated in the retina of the closed eye and the other was enriched in cDNAs potentially down-regulated. One thousand
clones from each library were organized in 384-well plates. Bacterial clones
from these plates were manually printed onto nylon filters using a 384-pin tool
(V&P Scientific, San Diego, CA) to prepare two identical sets of bacterial
colony filters. These filters were hybridized with subtracted probes, and 535 differentially-expressed cDNAs were amplified by PCR, purified, dried and resuspended in 5xSSC. The cDNA library was then spotted onto glass slide using QArray2 microarrayer.


title: UofToronto-yeastORF-6.4k4

last: Silver


title: KUL Human 4K_2 BAC array Aneuploidy Screening

status: Public on Feb 15 2006

city: Leuven

first: Joris

middle: R

last: Vermeesch

address: Herestraat, 49

department: Center for Human Genetics

country: Belgium

institute: Katholic University Leuven

description: An array containing 3,475 BAC and PAC clones at an average resolution of 1 Mb (Fiegler et al. 2003), 96 additional clones (RP clones; plate 1, offset A1) for each of the chromosomes 18, 19, 20, 21 and 22 from the Human 32K BAC Re-Array of CHORI BACPAC Resources, and 58 home-made clones (CME), was used, resulting in an array with 4,013 clones, amplified by DOP-PCR.

first: Cedric

last: Le Caignec

first: Paul

last: Van Hummelen

first: Bernard

last: Thienpont

manufacture_protocol: As described in Vermeesch JR et al. J Histochem Cytochem 2005;53:413-422.


title: ORNL Shewanella oneidensis 11.5k array

first: XiaoYun

last: Qiu

address: 200 longwood Ave

department: Microbiology and Molecular Genetics

organism: Shewanella oneidensis MR-1

description: The ArrayIt® brand SuperAmine 2 Microarray Substrates line represents the highest quality amine-containing substrate in the microarray industry. All of our substrates are polished to atomic flatness and manufactured in a state-of-the-art class 100 cleanrooms, with strict controls on particulate, biological and static contaminants, as well as temperature and humidity control.  These pristine glass substrates with reactive amine groups offer quality and performance that cannot be obtained from any other vendor.

first: Jizhong

last: Zhou

first: Liyou

last: Wu

first: James

last: Cole

first: Joel

last: Klappenbach

last: Tiedje

manufacture_protocol: The predicted ORFs of Shewanella oneidensis MR-1 (NC_004347) are PCR amplified. The PCR amplicons are deposited onto Telechem Superamine slide (Telechem, Inc., Sunnyvale, Calif.) in duplicate. There are 32 blocks on the array. In each block, there are 18 columns and 20 rows. See detailed description on manufacture protocol in "Global Transcriptome Analysis of the Heat Shock Response of Shewanella oneidensis" (J. Bacteriol. Vol 186, No.22: 7796-7803).


title: Arabidopsis mitochondrial retrograde regulation array_2

status: Public on Feb 02 2006

city: East Lansing

first: Jianping

last: Yu

state: MI

address: Michigan State University

department: Plant Research Laboratory

institute: Michigan State University

organism: Arabidopsis thaliana

first: Lee

last: McIntosh

first: Roxy

last: Nickels

first: Per

last: Gardestrom

manufacture_protocol: Schaffer et al., 2001. Plant Cell 13: 113-123, PMID: 11158533, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=search&DB=pubmed&term=11158533


title: miRNA microarray

status: Public on Feb 01 2006

city: Research Triangle Park

first: Michael

middle: D.

last: Mattie

state: NC

address: Five Moore Drive

department: Genomics Research

institute: GlaxoSmithKline

manufacturer: Haqq Lab, University of California San Francisco

first: Christopher

last: Haqq

middle: D

manufacture_protocol: Printing, post-processing, and analysis of the microarrays was performed as described (www.microarrays.org). An oligonucleotide microarray was constructed containing all of the annotated human microRNA genes in the miRNA Registry (www.sanger.ac.uk/Software/Rfam/mirna/).  Oligonucleotide probes identical to the sense orientation of the mature human miRNA sequences were synthesized by Operon Biotechnologies (Huntsville, AL) and duplicate spotted in 3X SSC on Gold Seal microslides (Becton Dickinson, Bedford, MA) coated with poly-l-lysine using a linear servo arrayer at the UCSF Core Facility for Genomics and Proteomics.  Post-printing processing was performed using succinyl anhydride as described (http://microarrays.org).  Arrays were printed with probes consisting of a tandem repeat or dimer of the mature sequences.  At the time of printing the arrays contained all of the annotated human microRNA genes in the miRNA Registry as of November, 2004 (approximately 200).  A total of 14 negative control sequences were also printed on the array.  These sequences are reverse sequences of selected miRNAs.  We have not observed any binding of sequences to any of the negative controls.


title: Invitrogen Yeast Protoarray

status: Public on Feb 08 2006

city: Aurora

first: Jay

middle: R.

last: Hesselberth

state: CO

department: Biochemistry and Molecular Gentetics

institute: University of Colorado School of Medicine

technology: spotted peptide or protein

description: The Yeast ProtoArray™ high-density functional protein microarray is the first microarray product that enables rapid elucidation of proteinprotein interactions on a proteome scale. The Yeast ProtoArray™ contains 4,088 S. cerevisiae open reading frames (ORFs) expressed as 5'-GST fusions, purified and spotted in duplicate on a 1 inch x 3 inch nitrocellulose-coated slide (Figure 1).With the Yeast ProtoArray™ PPI Kit, you can identify novel protein interactions in a single day, instead of the several weeks required using alternatives such as yeast two-hybrid systems. In addition, protein interactions can be easily assayed under different conditions to better understand interaction dynamics.

distribution: commercial

first: John

middle: P

last: Miller

first: Gregory

middle: A

last: Michaud

manufacture_protocol: The yeast proteome collection was derived from the yeast clone collection of 5800 yeast ORFs.  The identity of each clone was verified using 5' end sequencing.  Expression of glutathione-S-transferase (GST)-tagged protein by each clone was tested using Western blotting and detection with an anti-GST antibody.  The 4088 clones that passed both quality control measures were purified using high-throughput affinity chromatography as previously described.  A contact-type printer (Omnigrid, Genomic Solutions) equipped with 48 matched quill-type pins was used to deposit each of 4,088 purified yeast proteins along with a set of control elements in duplicate spots on 1" x 3" glass slides. The printing of these arrays was carried out in a cold room under dust-free conditions in order to preserve the integrity of both samples and printed microarrays.  Before releasing these protein microarrays for use, each lot of slides is subjected to a rigorous quality control procedure, including a gross visual inspection of all the printed slides for imperfections.  The second step consists of a more detailed characterization of each spot on the array.  Since each of the proteins is tagged with GST, this QC procedure is accomplished by using an antibody detection protocol specific for GST.  This procedure measures the variability in spot morphology, the number of missing spots, the presence of control spots, and the amount of protein deposited in each spot.


title: EGD-e microarray platform

status: Public on Feb 11 2006

first: Aimee

last: Shen

address: Armenise Building, rm 313, 200 Longwood Avenue

institute: Harvard University

organism: Listeria monocytogenes

description: Note that the ID number given is the product of the TIGR ID and the sum of (block+column+row).

manufacture_protocol:
Listeria monocytogenes
The Listeria monocytogenes genome microarray consists of 6347 70-mer oligonucleotides representing ORFs from:

Listeria monocytogenes - strain EGD-e
Listeria monocytogenes - strain 4b F2365
Listeria monocytogenes - strain 1/2a F6854
Listeria monocytogenes - strain 4b H7858
printed on amino-silane Nexterion A Schott slides


title: Arabidopsis mitochondrial retrograde regulation array_1


title: KUL Human 4k BAC array Aneuploidy Screening

first: Joris

last: Vermeesch

description: An array containing 3,587 BAC and PAC clones at an average resolution of 1 Mb (Fiegler et al. 2003), 96 additional clones (RP clones; plate 1, offset A1) for each of the chromosomes 18, 19, 20, 21 and 22 from the Human 32K BAC Re-Array of CHORI BACPAC Resources, and 47 home-made clones (CME), was used, resulting in an array with 4,114 clones, amplified by DOP-PCR.

first: Paul

last: Van Hummelen

first: Cedric

last: Le Caignec

last: Thienpont

manufacture_protocol: As described in Vermeesch et al. J Histochem Cytochem 2005;53:413-422.


title: Compugen Mouse OligoLibrary 2.0

status: Public on Feb 14 2006

city: Augusta

first: Yutao

last: Liu

state: GA

address: 1120 15th Street

department: Cellular Biology and Anatomy

institute: Augusta University

description: The oligonucleotides are 65mers

first: Brynn

last: Voy

manufacture_protocol:
Please refer to the below:
Hu, R., Hebbar, V., Kim, B-R., Chen, C., Winnik, B., Buckley, B., Soteropoulos, P., Tolias, P., Hart, R.P, and Kong, A-N.T. (2004) In vivo pharmacokinetics and pegulation of gene expression profiles by isothiocyanate sulforaphane in the rat. J. Pharmacol. Exp. Ther. 310, 263-71.


title: TIGR 40K Human array

city: Washington

first: Valerie

middle: Wailin

last: Hu

state: DC

department: Biochemistry and Molecular Medicine

institute: The George Washington University School of Medicine and Health Sciences

manufacture_protocol: Spotted cDNA arrays


title: WU Sigma Mus musculus 21K

city: St. Louis

first: Xiaobo

last: Lin

state: MN

address: 660 S. Euclid Ave.

institute: Washington University School of Medicine

description: The 21,676 mouse 65-mer oligo array was purchased from Sigma

manufacture_protocol: Slide with 21,676 oligos from Sigma 65-mer Probe Set


title: Xylella USP microarray v1 (Koide et al. 2004 J.Bact.)

status: Public on Feb 04 2006

city: Ribeirao Preto

first: Ricardo

last: Vêncio

state: SP

address: Av. Bandeirantes, 3900

department: Computing and Mathematics Department

country: Brazil

institute: Universidade de São Paulo

organism: Xylella fastidiosa

manufacturer: Instituto de Química da Universidade de São Paulo (IQ-USP)

first: Tie

last: Koide

first: Paulo

last: Zaini

manufacture_protocol:
A 4608-spot DNA microarray was printed containing unique internal fragments of 2572 CDS representing 90.3% of all of the 2848 CDS annotated by Simpson et al. (2000, Nature) (http://aeg.lbi.ic.unicamp.br/xf).

PCR primers were designed to amplify unique internal fragments of 200-1000 bp of each predicted CDS described in the annotated genome sequence of X. fastidiosa strain 9a5c (http://aeg.lbi.ic.unicamp.br/xf). Primers (18-23mers) with equivalent predicted melting temperature were designed with the use of a perl program that ran PRIMER3 for the complete CDS list, automatically testing many parameter settings and also guaranteeing that primers hybridized only to a single genome location. A full list of primers, PCR product sizes, and their nucleotide sequences are available at the project site (http://verjo19.iq.usp.br/xylella/microarray/).

Oligonucleotides were synthesized by MWG. Genomic or cosmid DNA, obtained in the X. fastidiosa genome sequencing project, were used as template in the first round of PCR amplification, and 200-fold-diluted PCR products were used as templates for PCR reamplification to increase product concentration when necessary. The reactions were done in 96-well plates. The mixture in each well contained 100 ng of DNA, 0.5 U of Biolase Taq polymerase (Bioline), 0.2 mM of each dNTP (Invitrogen), 1.5 mM MgCl2 and the primers at 0.5 µM, in a total volume of 100 µl. A 5min denaturing step at 95°C was applied, followed by 40 cycles of 95°C for 45s, 50°C for 30s, 72°C for 1min and a final step at 72°C for 10min. 4 µl of each PCR reaction were checked for product size and concentration by electrophoresis in 1.2% agarose gels. The amplicons were then purified with 96-well MultiScreen purification plates (Millipore) and an equal volume of dimethyl sulfoxide was added to the purified products (~100 ng/µl final concentration).

Generation III DNA spotter (Amersham Biosciences) was used to array the samples onto coated type-7 glass slides (Amersham Biosciences). This spotter arrays two technical replicas of each sample, one in each longitudinal half of the slides. However, this platform describes only one side of the replicated sides.

After deposition, the spotted DNA samples were crosslinked to the coated slides by applying 50 mJ of UV light and the slides were stored desiccated at ~10% relative humidity at room temperature until use.


title: GIS 22k Compugen Mm Oligo Microarray

city: Singapore

first: Huck Hui

last: Ng

state: Singapore

address: 60 Biopolis street, #02-01 Genome

department: Cell and Medical Biology

country: Singapore

institute: Genome Institute of Singapore

first: Lance

manufacture_protocol: 60-oligomer acquired from Compugen (MOULIB96T) spotted on Poly-L-Lysine coated slides (using a custom-made microarrayer develop by Joe DeRisi ); UV-cross-inked and blocked with succinate anhydride/boric acid/1-M-2-Pyrrolidinone; washed with water and ethanol; dried by centrifugation @ 100 xg


title: CodeLink Uniset Mouse 20K Bioarray

city: Houston

first: Huiping

last: Zhu

address: 2121 W. Holcombe Blvd

department: Center for Environmental and Genetic Medicine

institute: Institute of Biosciences and Technology, TAMUSHSC