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Status |
Public on Jun 01, 2012 |
Title |
embryo at HH8_NP_rep3 |
Sample type |
RNA |
|
|
Source name |
cranial neural plate, HH8
|
Organism |
Gallus gallus |
Characteristics |
embryo stage: HH8 tissue: cranial neural plate (NP)
|
Treatment protocol |
Cranial neural folds and neural plates were dissected from HH stage 8 embryos using tungsten needles in ice-cold Hank's balanced salt solution with supplemented with 1 mM MgCl2, 1 mM CaCl2, and 1 mM HEPES at pH 7.5.
|
Growth protocol |
Fertile chicken eggs were incubated at 38C in a humidified incubator.
|
Extracted molecule |
total RNA |
Extraction protocol |
The isolated tissues were dissolved in TRIzol (Invitrogen), snap frozen in dry ice/ethanol, and then stored at -80C overnight. Total RNA were isolated according to the manufacturer's protocol.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
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|
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Hybridization protocol |
Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Chicken Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
|
Scan protocol |
GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
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Data processing |
The data were analyzed with Affymetrix GeneChip Operating System (GCOS) 1.x using Affymetrix MSA5 default analysis settings and global scaling as normalization method.
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|
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Submission date |
May 31, 2012 |
Last update date |
Jun 01, 2012 |
Contact name |
Yukinori Endo |
E-mail(s) |
[email protected]
|
Phone |
301-827-0737
|
Fax |
301-496-1810
|
Organization name |
NIDCR, NIH
|
Department |
Laboratory of Cell and Developmental Biology
|
Lab |
Cell Biology Section
|
Street address |
30 Convent Drive, MSC 4370, Room 402
|
City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
|
|
Platform ID |
GPL3213 |
Series (1) |
GSE38381 |
Chicken neural crest and neural plate |
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