NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1145999 Query DataSets for GSM1145999
Status Public on Aug 31, 2013
Title sm_normal_cultured_strains_rep1
Sample type RNA
 
Source name normal cultured strains
Organism Streptococcus mutans UA159
Characteristics genotype: Wild type
phenotype: normal
accession: NC_004350
Growth protocol For the control group, the S.mutans UA159 strains were cultured in brain heart infusion broth (BHI; Difco, Sparks, MD) at 37℃ in a 5% CO2 atmosphere to mid-logarithmic phase.
For the hyperosmotic stimuli group, the S.mutans UA159 strains were cultured in brain heart infusion broth (BHI; Difco, Sparks, MD) at 37℃ in a 5% CO2 atmosphere to mid-logarithmic phase. Then the strains were submitted for 15 minutes to hyperosmotic stimuli (0.4M NaCl).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the RNAProtect Bacteria Reagent (Qiagen) and RNeasy Mini kits (Qiagen). Rnase-Free DNase Set (Qiagen) was used to remove genome DNA. A Nanodrop ND 1000 spectrophotometer (Thermo Scientific) was used to confirm total RNA concentrations, while an Agilent 2100 Bioanalyser (Agilent Technologies, CA, USA) was used to evaluate the RNA quality. The isolated RNA was stored at -80℃ until use.
Label Cy3
Label protocol Labeling was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
 
Hybridization protocol Hybridization was performed by NimbleGen Systems Inc., Madison, WI, USA following their standard operating protocol. See www.nimblegen.com.
Scan protocol Scanning was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
Description This sample is of S. mutans UA159 cultured in the normal condition. It is the first of three normally cultured biological replicates used in this experiment, each from separate cultures.
Data processing The raw data (.pair file) was subjected to RMA algorithm normalization and background correction as implemented in the NimbleScan software package, version 2.6 (Roche NimbleGen, Inc.).
 
Submission date May 22, 2013
Last update date Aug 31, 2013
Contact name Yulong Niu
E-mail(s) yulong.niu@hotmail.com
Organization name Max Planck Institute for Plant Breeding Research
Department Plant Microbe Interactions
Street address Carl-von-Linne-Weg 10
City Köln
State/province Nordrhein-Westfalen
ZIP/Postal code 50829
Country Germany
 
Platform ID GPL17184
Series (1)
GSE47170 Expression analysis of Streptococcus mutans UA159 under Hyperosmotic stress environment

Data table header descriptions
ID_REF
VALUE RMA-normalized, averaged gene-level signal intensity

Data table
ID_REF VALUE
SMU_01 13.0081
SMU_02 12.7915
SMU_05 8.9842
SMU_06 11.9979
SMU_07 10.2521
SMU_08 10.4845
SMU_09 10.7048
SMU_10 11.0822
SMU_100 9.6408
SMU_1000 5.0172
SMU_1001 7.8137
SMU_1002 11.7355
SMU_1003 12.3207
SMU_1004 10.8552
SMU_1005 13.7151
SMU_1006 9.9652
SMU_1007 11.3916
SMU_1008 10.679
SMU_1009 12.4596
SMU_101 11.7871

Total number of rows: 1949

Table truncated, full table size 31 Kbytes.




Supplementary file Size Download File type/resource
GSM1145999_sm3701.pair.gz 1.0 Mb (ftp)(http) PAIR
GSM1145999_sm3701.txt.gz 16.4 Kb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap