|
Status |
Public on Oct 17, 2006 |
Title |
siFBP1_Set B - 2nd array - mAdbID:74111 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
Set B_control siRNA
|
Organism |
Homo sapiens |
Characteristics |
Cell type: primary skin fibroblast (Hs68)
|
Treatment protocol |
Treatment type: compound Agent: Stealth negative control siRNA Treatment dose: 50 nM Treatment time: 2 days
|
Extracted molecule |
total RNA |
Extraction protocol |
Sample Extraction Protocol Extraction method: Trizol
|
Label |
cy3
|
Label protocol |
Cy3 Sample Labeling Protocol - generic
|
|
|
Channel 2 |
Source name |
Set B_siFBP1
|
Organism |
Homo sapiens |
Characteristics |
Cell type: primary skin fibroblast (Hs68)
|
Treatment protocol |
Treatment type: compound Agent: Stealth siRNA targeting FBP1 Treatment dose: 50 nM Treatment time: 2 days
|
Extracted molecule |
total RNA |
Extraction protocol |
Sample Extraction Protocol Extraction method: Trizol
|
Label |
cy5
|
Label protocol |
Cy5 Sample Labeling Protocol - generic
|
|
|
|
Hybridization protocol |
NCI Oligo Microarray Hybridization Other: For pre-hybrization, apply 40 ul of pre-hybridization buffer (5X SSC, 0.1% SDS, 1% BSA) to the array and incubate at 42øC for at least 30 minutes and up to an hour. Wash off the pre-hybridization solution by rapidly plunging the slide in distilled water for 2 minutes, then transfer slide to 100% isopropanol for 2 minutes. Allow slide to air dry completely prior to use. (Can spin dry if in a rush.) (NOTE: Do not exceed 1 hour after pre-hybridization/drying before setting up hybridization.) For hybridization, combine Cy3 and Cy5 labeled targets together (~9 ul recovered for each). Add 1 ul COT-1 DNA (8-10 ug/ul) and 1 ul poly A (8-10 ug/ul). Denature target at 100øC for 1 minute, then snap cool on ice. (Final volume should be about 20 ul.) Make fresh 2X Formamide hybridization buffer (50% formamide, 10X SSC, 0.2% SDS) and warm to 42øC just before adding to samples. Add 20 ul of 2X F-hyb buffer to samples. Load 40 ul sample onto microarray. Add 20 ul of 3X SSC to wells in hyb chamber to maintain humidity. Incubate overnight (12-16 hours) at 42øC in water bath or hybridization oven. After hybridization of slides, wash slides for 2 minute in 2X SSC with 0.1% SDS (with occasional plunging), for 2 minute in 1X SSC (with occasional plunging), for 2 minutes in 0.2X SSC (with occasional plunging), and spin for 3 minutes at 650 rpm to dry. (Refer to "NCI Microarray Manual")
|
Description |
mAdb experiment ID: 74111
|
Data processing |
After background correction and removal of flagged values, log base 2 expression ratios were median centered and linear transformed to obtain the log and linear values given in the data table.
|
|
|
Submission date |
May 24, 2006 |
Last update date |
Oct 17, 2006 |
Contact name |
David Levens |
E-mail(s) |
levens@helix.nih.gov
|
Phone |
301-496-2176
|
Fax |
301-402-0043
|
Organization name |
NIH
|
Department |
NCI/CCR
|
Lab |
LP
|
Street address |
10 Center Drive
|
City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
|
|
Platform ID |
GPL3779 |
Series (1) |
GSE4914 |
RNAi analysis of the FBP transactivator family |
|
Data table header descriptions |
ID_REF |
NCI mAdb well id plus replicate number |
VALUE |
same as UNF_VALUE but with flagged values removed |
Ratio |
Calibrated Ratio (CY5 channel/CY3 channel) |
Slide_block |
Array block location |
Slide_column |
Array column location |
Slide_row |
Array row location |
CY5_mean |
Red Channel Sample mean Signal (Background Subtracted) |
CY5_SD |
Red Channel Sample Standard Deviation |
CY5_BKD_median |
Red Channel Sample median Background Level |
CY5_BKD_SD |
Red Channel Sample Background Standard Deviation |
CY3_mean |
Green Channel Sample mean Signal (Background Subtracted) |
CY3_SD |
Green Channel Sample Standard Deviation |
CY3_BKD_median |
Green Channel Sample median Background Level |
CY3_BKD_SD |
Green Channel Sample Background Standard Deviation |
Flag |
Quality flag 0->good, -50->Not found, -100->Bad |
UNF_VALUE |
log2 ratio |