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Sample GSM801246 Query DataSets for GSM801246
Status Public on Apr 03, 2013
Title embryo injected with anti-mir-34LNA, kept for 7hpf, biological rep2
Sample type RNA
 
Source name embryo injected with anti-mir-34LNA, kept for 7hpf
Organism Danio rerio
Characteristics genotype: wild type
tissue: anti-mir-34LNA injected embryos, dechorionated
embryo age: 7 hour post fertilization
Treatment protocol Embryos were collected at one cell stage. Embryos were injected with anti-mir-34LNA of mockLNA at the 1-2 cell stage and were harvetyes at the specified time points of 1hpf, 7hpf and 24hpf. The embryos were also monitoredunder the dissecting microscope for any developmental abnormalities of phenotypic defects. Selected embryos were transferred to a fresh petriplate. The injected embryos at 7hpf and 24hpf were dechorionated manually, rinsed with distilled water and placed on ice in the Trizol solution (GibcoBRL).
Growth protocol 1-2 cell stage embryos were collected for microinjection. Following injections the embryos were aged at 30C and were lated collected at the different time points (1hpf, 7hpf and 24hpf)
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol as per the manufacturer's instructions.
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).
 
Hybridization protocol Following fragmentation, 20 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Zebrafish 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.
Description Gene expression data from Zebrafish embryos at 7 hour post fertilization(hpf) indicating transcript pool during maternal to zygotic transcription
Data processing Initial QC and processing was done using Affymetrix GeneChip Operating Software(GCOS) to obtain the raw signal intensities. The data were analyzed with Avadis using the default analysis settings and quantile normalization as normalization method afer being log transformed.
 
Submission date Sep 23, 2011
Last update date Apr 03, 2013
Contact name Kartik Soni
E-mail(s) kartik@igib.in
Organization name INSTITUTE OF GENOMICS AND INTEGRATIVE BIOLOGY
Department FGU
Lab MOL. BIO
Street address Mathura Road
City NEW DELHI
State/province NA
ZIP/Postal code 110028
Country India
 
Platform ID GPL1319
Series (1)
GSE32360 Expression data from early Zebrafish embryos after knockdown of mir-34

Data table header descriptions
ID_REF
VALUE log2 quantile normalized
Detection_Call

Data table
ID_REF VALUE Detection_Call
Dr.25895.1.A1_at A
Dr.14202.1.S1_s_at 0.9356804 A
Dr.20553.2.A1_a_at 12.115044 P
Dr.815.1.S1_at 4.296159 A
Dr.20553.1.A1_x_at 11.989473 P
AFFX-Dr-acta1-3_at 2.5950336 A
Dr.815.1.S1_x_at 4.6039705 A
Dr.1065.1.S1_at 10.714935 P
Dr.11308.1.S1_at 11.056427 P
Dr.1126.1.A1_at 11.125729 P
Dr.4412.4.S1_at 10.734366 P
Dr.1368.1.S1_a_at 11.64827 P
Dr.2417.2.S1_at 10.598856 P
Dr.1345.1.S1_at 10.062557 P
Dr.4387.2.S1_at 11.156269 P
Dr.261.1.S1_at 11.648913 P
Dr.1054.1.S1_at 11.00946 P
Dr.25564.1.S1_at 10.400732 P
Dr.20553.1.A1_at 11.8324 P
Dr.1313.1.S1_at 10.608348 P

Total number of rows: 15617

Table truncated, full table size 435 Kbytes.




Supplementary file Size Download File type/resource
GSM801246_34a_7hpf_2.CEL.gz 1.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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