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View additional product information for GeneChip™ HT RG-230 PM Array Plate - FAQs (901259)
9 product FAQs found
The hybridization mix for PEG arrays is different from the hybridization mix for cartridges. The concentrations of the hybridization mix are different and in addition, DMSO is not added into the hybridization mix for PEG arrays because it can affect the glue that holds the PEG to the plate.
96 arrays = 4-4.6 hours
24 arrays = 1.5-2 hours
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No, continue to finish products using the same procedures and products. New projects can be moved to PM only arrays.
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Mean absolute relative log expression: MA (RLE)
-Detection of 20X spikes, Bio B, Bio C, Bio D & Cre
-House keeping controls
-Poly A controls
-Antigenomic GC - 12 background probes
-PM mean
Please refer to the QC Metrics for Human, Mouse and Rat HT PM Array Plates QRC for more information (http://tools.thermofisher.com/content/sfs/manuals/ hmr_qc_metrics_qrc.pdf).
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We recommend running the RMA algorithm in the Transcriptome Analysis Console (TAC).
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MAS5 requires the use of Mismatch probes which the HT PM Plate Arrays do not currently use.
MAS5 can be used with the Advanced Configuration however the software will automatically shut down if analysis is run.
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No, %P is a metric derived using the MAS5 algorithm which has been disabled for the HT PM Plate Arrays.
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No, new scripts for Hyb, Wash, and Stain of the HT HMR PM only array plates will not be needed. The script is the same as the old HMR plate arrays.
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No, the PM only arrays have probes that are perfect match only. The mismatch probes have been removed. For the HT HGU133 plus PM product roughly 3/4 of the probesets have 9 probes, a small portion has 10; the remaining probesets have 11. The Mouse and Rat PM only plate arrays utilize all 11 probes for each probeset.
Find additional tips, troubleshooting help, and resources within our Microarray Analysis Support Center.