| 1 |
GPL1465 |
BCM-NIA15k |
16,128 |
Baylor College of Medicine |
2004-09-22 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, BCM-NIA15k, BCM-NIA15k array |
| 2 |
GPL1450 |
15k-1/3 |
5,760 |
National Institutes of Health |
2004-09-15 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, 15k-1/3, NIA mouse 15k cDNA clone set 1 of 3 |
| 3 |
GPL1451 |
15k-2/3 |
5,760 |
National Institutes of Health |
2004-09-15 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, 15k-2/3, NIA mouse 15k cDNA clone set 2 of 3 |
| 4 |
GPL1452 |
15k-3/3 |
5,760 |
National Institutes of Health |
2004-09-15 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, 15k-3/3, NIA mouse 15k cDNA clone set 3 of 3 |
| 5 |
GPL1440 |
LUNDNIH_Mouse_37K_1 |
37,632 |
Lund University |
2004-09-09 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, LUNDNIH_Mouse_37K_1, Mouse cDNA 37K |
| 6 |
GPL1441 |
LUNDNIH_Mouse_37K_2 |
37,632 |
Lund University |
2004-09-09 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, LUNDNIH_Mouse_37K_2, Mouse cDNA 37K |
| 7 |
GPL1437 |
Mouse miRNA chip |
21,939 |
Best Institute |
2004-09-06 |
|
Mus musculus
 |
Tiling Array |
spotted DNA/cDNA, Mouse miRNA chip, We describe a method to detect miRNAs using microarrays, in which the miRNAs are directly hybridized to the array. We used this method to analyze miRNA expression across 16 mouse organs and tissues. More than half of the 78 miRNAs detected were expressed in specific adult tissues. By comparing miRNA levels to mRNA levels determined in a parallel microarray analysis of the same tissues, we found that the expression of target mRNAs predicted on the basis of sequence similarity is biased towards the tissues in which the corresponding miRNA is expressed. The data shown here includes data for 361 other ncRNAs as positive controls. Probes were generated by tiling across each transcript, including 100 nucleotides of flanking sequence extracted from genomic sequence. Keywords = miRNA mouse |
| 8 |
GPL1427 |
NMC_Rat_15k_cDNA_Ser6 |
30,000 |
Norwegian University of Science and Technology |
2004-08-31 |
|
Rattus norvegicus
 |
cDNA Array |
spotted DNA/cDNA, NMC_Rat_15k_cDNA_Ser6, The 15k rat cDNA arrays were prepared from a collection of 14k cDNAs purchased from Research Genetics (Huntsville, AL) (http://www.mikromatrise.no). Plasmids were isolated from overnight bacterial cultures in 96-well plates and cDNA inserts amplified by PCR using M13 primers 5'-ctg caa ggc gat taa gtt ggg taa c and 5'-gtg agc gga taa caa ttt cac aca gga aag a. The PCR products were purified with Montage PCR purification kit (Millipore) and quality and concentration was assessed by agarose gel electrophoresis. The purified PCR products were dissolved in 50% DMSO (about 50-200 ng/ l) and spotted in duplicate onto 25 x 75mm amino-silane coated CMT-GAPS glass slides (Corning, NY) using a MicroGrid II printing robot (BioRobotics; Cambridge, UK). The arrays were spotted with 48 pins and contained 4 x 12 blocks of 25 x 25 spots. The probes were fixed to the slide surface by UV irradiation (200 mJ). The 15k cDNA arrays represent 14018 unique probes, all printed in duplicates. In addition, a few in-house cDNA probes and a set of positive and negative control elements including 10 different PCR products of exogenous DNA from SpotReportâ„¢ cDNA Array Validation System (Stratagene, La Jolla, CA) were printed on the arrays. Totally, each array contained 30000 elements including duplicates and controls. |
| 9 |
GPL1425 |
Rat 2K Array |
4,608 |
Medical College of Wisconsin |
2004-08-30 |
|
Rattus norvegicus
 |
GeneChip |
spotted DNA/cDNA, Rat 2K Array, The custom microarrays were manufactured by the Department of Physiology at the Medical College of Wisconsin. Microarrays were printed with a GMS 417 robotic arrayer from Affymetrix (made by Genetic Microsystems) that has a printhead with 4 pin-and-ring print tips. Arrays were prepared from the first 18 of 88 plates of a rat cDNA library from Research Genetics. The clone set represents 1631 known genes and 192 ESTs. We included 506 negative control spots and 456 positive control spots. Following amplification, PCR amplicons were distributed into 384-well polypropylene plates (Genetix, 384 micro array), resuspended in 50% DMSO and printed onto poly-L-lysine coated glass slides. Print configuration is 8 blocks in a 2 x 4 arrangement. Positive controls were printed in each block, and included beta-actin and GAPDH. Negative controls were also printed in each block, and included 5 Arabidopsis gene fragments, mouse COT-1, DMSO, poly dA, yeast tRNA, and PCR buffer with and without primers. The microarray spot density is 250 microns (center-to-center). Spot diameters are approximately 120-150 microns. After printing, DNA was cross-linked to the slides by UV irradiation at 65 mJ (Stratalinker UV Crosslinker, Stratagene). The microarrays were post-processed according to the procedures on the Stanford website (http://cmgm.stanford.edu/pbrown/protocols/index.html) and subsequently stored at room temperature in a desiccated chamber until use. |
| 10 |
GPL1415 |
Rat 8Kx2 cDNA array |
16,128 |
Johns Hopkins University |
2004-08-24 |
|
Rattus norvegicus
 |
cDNA Array |
spotted DNA/cDNA, Rat 8Kx2 cDNA array, Rat 8Kx2 cDNA microarrays were obtained from the Johns Hopkins Cancer Center Microarray Core (Baltimore, MD). They contain 8000 genes and ESTs, double-printed on-site, from a cDNA set generated by The Institute for Genomic Research (Rockville, MD). |
| 11 |
GPL1413 |
GSF mouse array |
20,419 |
GSF - National Research Center |
2004-08-23 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, GSF mouse array, cDNA array of commercially available set of 20.400 clones (Mus musculus) and specific mouse genes spotted on aldehyde coated slides. |
| 12 |
GPL1406 |
IncyteMouseGEM1 |
8,734 |
Cincinnati Children's Hospital Medical Center |
2004-08-12 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, IncyteMouseGEM1, IncyteMouseGEM1 (127 cloneID) |
| 13 |
GPL1397 |
Compugen Rat 5K - 65nt |
4,803 |
Leiden University Medical Center |
2004-08-09 |
Compugen, Sigma Genosis |
Rattus norvegicus
 |
Oligo Array |
spotted oligonucleotide, Compugen Rat 5K - 65nt, Compugen 5K rat oligonucleotide library, 5' C6-amino modifier printed on CodeLink Activated Slides |
| 14 |
GPL1388 |
Mice microarray for muscular dystrophy analysis (Layout 1). |
1,200 |
INSERM |
2004-07-29 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, Mice microarray for muscular dystrophy analysis (Layout 1)., The microarray 1082 different cDNA clones (with 93 non-annotated), issued from four subtractive libraries, previously prepared by suppressive/subtractive hybridizations between control and mdx hindlimb muscles, and between control and mdx DIA muscles of 12 week-old mice. |
| 15 |
GPL1389 |
Mice microarray for muscular dystrophy analysis (Layout 2). |
1,200 |
INSERM |
2004-07-29 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, Mice microarray for muscular dystrophy analysis (Layout 2)., The microarray 1082 different cDNA clones (with 89 non-annotated), issued from four subtractive libraries, previously prepared by suppressive/subtractive hybridizations between control and mdx hindlimb muscles, and between control and mdx DIA muscles of 12 week-old mice. |
| 16 |
GPL1371 |
TESSF393 |
4,968 |
TIGEM (Telethon Institute of genetics and Medicine) |
2004-07-23 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, TESSF393, TESS library is a collection of genes preferentially expressed in the embryonic telencephalon. cDNA clones of library TESS sequence validated, were amplified by PCR using primers that were complementary to the vector sequence. PCR products were robotically arrayed (PIXISYS) into lysine-coated slides (CMT-GAPSTM Coated Slides, Corning Microarray Technology). A total of 1026 cDNA clones were printed twice on each slides. |
| 17 |
GPL1374 |
TESS400-2 |
4,961 |
TIGEM (Telethon Institute of genetics and Medicine) |
2004-07-23 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, TESS400-2, TESS library is a collection of genes preferentially expressed in the embryonic telencephalon. cDNA clones of library TESS sequence validated, were amplified by PCR using primers that were complementary to the vector sequence. PCR products were robotically arrayed (PIXISYS) into lysine-coated slides (CMT-GAPSTM Coated Slides, Corning Microarray Technology). A total of 1026 cDNA clones were printed twice on each slides. |
| 18 |
GPL1369 |
UCSF Gladstone v.2 Oligo Array (6-2002) |
14,112 |
University of California, San Francisco |
2004-07-22 |
|
Mus musculus
 |
Oligo Array |
spotted oligonucleotide, UCSF Gladstone v.2 Oligo Array (6-2002), Spotted long oligonucleotide array on glass. The library used was the Qiagen/Operon v2.0 mouse oligo library, which is composed of oligonucleotides (70mers) representing 16,443 unique mouse genes. Keywords = spotted, long oligonucleotide |
| 19 |
GPL1368 |
TESS185 |
1,077 |
TIGEM (Telethon Institute of genetics and Medicine) |
2004-07-22 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, TESS185, TESS library is a collection of genes preferentially expressed in the embryonic telencephalon. cDNA clones of library TESS sequence validated, were amplified by PCR using primers that were complementary to the vector sequence. PCR products were robotically arrayed (PIXISYS) into lysine-coated slides (CMT-GAPSTM Coated Slides, Corning Microarray Technology). A total of 1026 cDNA clones were printed on each slides. |
| 20 |
GPL1356 |
TESS039 |
1,078 |
TIGEM (Telethon Institute of genetics and Medicine) |
2004-07-21 |
|
Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, TESS039, TESS library is a collection of genes preferentially expressed in the embryonic telencephalon. cDNA clones of library TESS sequence validated, were amplified by PCR using primers that were complementary to the vector sequence. PCR products were robotically arrayed (PIXISYS) into lysine-coated slides (CMT-GAPSTM Coated Slides, Corning Microarray Technology). A total of 1026 cDNA clones were printed on each slides. |
|