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Status |
Public on Oct 12, 2012 |
Title |
Primary Plasma Cell Leukemia PCL-021 Expression |
Sample type |
RNA |
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Source name |
Primary Plasma Cell Leukemia PCL-021
|
Organism |
Homo sapiens |
Characteristics |
cell type: plasma cell disease state: plasma cell leukemia genome variation: translocation t(4;14)
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Treatment protocol |
Plasma cells were purified from bone marrow samples using CD138 immunomagnetic microbeads according to the manufacturer's instructions (MidiMACS system, Miltenyi Biotec); the purity of the positively selected PCs was assessed by morphology and flow cytometry and was > 90% in all cases.
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Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions (Gibco BRL). RNA was purified using the Rneasy Mini Kit according to the manufacturer's instruction (Qiagen).
|
Label |
biotin
|
Label protocol |
5.5 micrograms of single-stranded DNA target obtained from 100 ng of purified total RNA was fragmented and then labeled using the WT Terminal Labeling Kit according to the standard Affymetrix protocol (GeneChip® Whole Transcript (WT) Sense Target Labeling Assay Manual).
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Hybridization protocol |
The fragmented labeled single-stranded DNA target was hybridized for 16 hours and 30 minutes at 45°C on GeneChip® Gene 1.0 ST array according to the standard Affymetrix protocol.
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Scan protocol |
Washing and scanning were performed using GeneChip System of Affymetrix (GeneChip Hybridization Oven 640, GeneChip Fluidics Station 450 and GeneChip Scanner 7G).
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Description |
main IgH chromosomal translocations t(11;14), t(4;14), t(14;16), t(14;20) Gene expression profiling data from human multiple myeloma patient PCL-021
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Data processing |
Log2-transformed expression values were extracted from CEL files and normalized using NetAffx Transcript Cluster Annotations, Release 31 and robust multi-array average (RMA) procedure in Expression Console software (Affymetrix Inc.). The expression values of transcript cluster ID specific for loci representing naturally occurring read-through transcriptions were summarized as median value for each sample.
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Submission date |
Jul 16, 2012 |
Last update date |
Oct 13, 2012 |
Contact name |
Luca Agnelli |
E-mail(s) |
luca.agnelli@istitutotumori.mi.it, luca.agnelli@gmail.com
|
Phone |
+390223903581
|
Organization name |
IRCCS Istituto Nazionale dei Tumori
|
Department |
Department of Advanced Diagnostics
|
Street address |
Venezian 1
|
City |
MILAN |
ZIP/Postal code |
20133 |
Country |
Italy |
|
|
Platform ID |
GPL6244 |
Series (2) |
GSE39381 |
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations (Expression) |
GSE39383 |
Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations |
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