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Status |
Public on Dec 17, 2008 |
Title |
CD11c+CD103+ versus CD11c+CD103- dendritic cells_replicate2_M2067 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
gProcessedSignal values originated from CD11c+CD103- dendritic cells
|
Organism |
Mus musculus |
Characteristics |
Bone marrow cells from CX3CR1+/gfp C57BL/6 mice were sorted as follows: lineage negative (CD3, CD19, NK1.1, Ter119, Ly6G and CD11c) CX3CR1+c-kit+. Sorted cells were further cultured in vitro under the continuous presence of GM-CSF. lin-CX3CR1+c-kit+ bone marrow cells gave rise to CD103- DC in vitro.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA is extracted with the RNeasy mini kit from QIAGEN as directed by the manufacturer.
|
Label |
Cy3
|
Label protocol |
cRNA-synthesis was performed with the “Low RNA Input Linear Amplification Kit PLUS, Two-Color” (#5188-5340, Agilent Technologies) as directed by the manufacturer.
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|
|
Channel 2 |
Source name |
rProcessedSignal values originated from CD11c+CD103+ dendritic cells
|
Organism |
Mus musculus |
Characteristics |
Bone marrow cells from CX3CR1+/gfp C57BL/6 mice were sorted as follows: lineage negative (CD3, CD19, NK1.1, Ter119, Ly6G and CD11c) CX3CR1+c-kit+. Sorted cells were further cultured in vitro under the continuous presence of GM-CSF. lin-CX3CR1+c-kit+ bone marrow cells gave rise to CD103- DC in vitro.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA is extracted with the RNeasy mini kit from QIAGEN as directed by the manufacturer.
|
Label |
Cy5
|
Label protocol |
cRNA-synthesis was performed with the “Low RNA Input Linear Amplification Kit PLUS, Two-Color” (#5188-5340, Agilent Technologies) as directed by the manufacturer.
|
|
|
|
Hybridization protocol |
cRNA fragmentation, hybridization and washing steps were performed exactly as recommended by the manufacturer “Two-Color Microarray-Based Gene Expression Analysis Protocol V5.0.1” (see http://www.agilent.com for details).
|
Scan protocol |
Slides were scanned on the Agilent Micro Array Scanner G2505 B at two different PMT settings, namely 100% and 5%, to increase the dynamic range of the measurements.
|
Description |
Log ratio values were calculated by dividing rProcessedSignal values by gProcessedSignal values, thus positive log ratio values indicate enhanced mRNA expression levels within the CD11c+CD103+ dendritic cell population.
|
Data processing |
Data extraction and normalization were performed with the “Feature Extraction Software V9.1.3.1” by using the recommended default extraction protocol file: GE2-v5_91_0806.xml.
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Submission date |
Mar 18, 2008 |
Last update date |
Dec 17, 2008 |
Contact name |
Oliver Dittrich-Breiholz |
E-mail(s) |
dittrich.oliver@mh-hannover.de
|
Organization name |
Medical School Hannover
|
Department |
Research Core Unit Genomics
|
Street address |
Carl-Neuberg-Str. 1
|
City |
Hannover |
ZIP/Postal code |
30625 |
Country |
Germany |
|
|
Platform ID |
GPL4134 |
Series (1) |
GSE10882 |
Transcription profile of CD103- vs CD103+ dendritic cells derived from CX3CR1+c-kit+- bone marrow cells (M1993 M2067) |
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