|
Status |
Public on Jan 30, 2009 |
Title |
NHMEC 98016 - dye swap - replicate 1 - mAdbID:53662 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
NHMEC 98016 (untreated) - Cy5
|
Organism |
Homo sapiens |
Characteristics |
Gender: female Tissue: mammary gland Cell line: NHMEC 98016 Cell type: Normal Human Mammary Epithelial
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol Extraction Protocol Other: For isolation of RNA the cells were lysed with 1.0 mL of Trizol Reagent (Invitrogen Corp., Carlsbad, CA) and RNA was extracted according to manufacturer’s protocol.
|
Label |
cy5
|
Label protocol |
Cy5 Labeling Protocol Other: Labeled with Cy5 by indirect coupling.
|
|
|
Channel 2 |
Source name |
NHMEC 98016 - TAM - Cy3
|
Organism |
Homo sapiens |
Characteristics |
Gender: female Tissue: mammary gland Cell line: NHMEC 98016 Cell type: Normal Human Mammary Epithelial
|
Treatment protocol |
Treatment type: compound Agent: Tamoxifen Treatment dose: 10 uM Treatment time: 48 hours Treatment temperature: 37C Other: Cells at passage 13 were plated at 1 x10^6 cells/15 cm plate or T-175 flask for DNA preparation, and at 1x10^6 cells/6-well plate for RNA preparation and survival, and grown for 48 hours prior to treatment with 10 uM TAM in vehicle (DMSO) for an additional 48 hours.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol Extraction Protocol Other: For isolation of RNA the cells were lysed with 1.0 mL of Trizol Reagent (Invitrogen Corp., Carlsbad, CA) and RNA was extracted according to manufacturer’s protocol.
|
Label |
cy3
|
Label protocol |
Cy3 Labeling Protocol Other: Labeled with Cy3 by indirect coupling.
|
|
|
|
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 42°C 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 100°C 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 42°C 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 42°C 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")
|
Scan protocol |
Creator: GenePix Pro 4.0.0.54 Scanner: GenePix 4000B [84573] ScanPower: 100;; 100 LaserPower: 3.37077;; 4.073 Temperature: 24.7093
|
Description |
mAdb experiment ID: 53662
|
Data processing |
mAdb Data Processing Protocol (v. 1) Calculation Method: 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 |
Nov 05, 2008 |
Last update date |
Jan 30, 2009 |
Contact name |
Ofelia Ana Olivero |
E-mail(s) |
oliveroo@exchange.nih.gov
|
Phone |
3014357843
|
Organization name |
NCI-CCR-
|
Department |
CDI
|
Lab |
LCBG
|
Street address |
37 Convent Dr-MSC 4255
|
City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
|
|
Platform ID |
GPL1528 |
Series (1) |
GSE13476 |
Tamoxifen induces expression of immune-response related genes in cultured NHMEC |
|
Data table header descriptions |
ID_REF |
NCI mAdb well id plus replicate number |
VALUE |
log ratio(log2 of Cy3/Cy5 channel) with flagged values removed |
PRE_VALUE |
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 |
log ratio (log2 of PRE_VALUE) |
INV_VALUE |
same as UNF_VALUE but with flagged values removed |