NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4559809 Query DataSets for GSM4559809
Status Public on Mar 11, 2024
Title V5-DDX39
Sample type protein
 
Source name V5-tagged DDX39 protein purified from HEK293T cells
Organism Homo sapiens
Characteristics cell line: HEK293T
recombinant protein expression: V5-DDX39
Treatment protocol HEK293T cells were transfected with 15 µg of the respective expression constructs using Calcium phosphate.
Growth protocol HEK293T cells were grown in 15 cm2 dishes at 37°C with 5% CO2 in DMEM medium supplemented with 10% fetal calf serum, 2 mM L-Glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin.
Extracted molecule protein
Extraction protocol Cells were lysed in 50 mM HEPES-KOH, pH 7.7, 1 mM MgCl2, 300 mM NaCl, 0.8 % Triton X-100, 5 mM NaF, 0.1 % Sodium deoxycholate, 2 mM β-mercaptoethanol, 1x protease inhibitor mixture tablet (Roche). Cleared lysates were immunoprecipitated using anti-V5 agarose beads (Roche) at 4 °C for 3 h. Beads were washed in TBS-T supplemented with 1 mM MgCl2, 2 mM β-mercaptoethanol and 1x protease inhibitor mixture tablet (Roche), followed by elution in the same buffer using 200 µg/ml V5 peptide.
Label Alexa Fluor 680
Label protocol Anti-mouse secondary antibody Alexa Fluor 680 (Thermo Fisher).
 
Hybridization protocol The protein microrrays (ProtoArray v5.1, Invitrogen) were incubated for 1 h at 4 °C in Blocking Buffer I (PBS, 0.1 % Tween-20, 1 % BSA). The arrays were washed three times at 4 °C in Blocking Buffer II (TBS supplemented with 0.5 % Triton X-100, 1 mM β-mercaptoethanol, 5 % Glycerol, 2 mM MgCl2, 1 % BSA), placed at room temperature and incubated for 1 h with 600 µl of ~ 0.5 µM of immunopurified V5-DDX39, V5-DDX56 or V5-GFP. The arrays were then washed twice in Blocking Buffer II at 4 °C and incubated with 1:1000 α-V5 tag monoclonal antibody (Thermo Fisher, R960-25) for 2 h at 4 °C. After three additional washes in Blocking Buffer II, the microarrays were incubated with anti-mouse secondary antibody Alexa Fluor 680 (Thermo Fisher) for 1 h at 4 °C and washed again three times. Finally, the arrays were rinsed 3 times in water and dried by spinning at 300 g for 5 min.
Scan protocol The microarrays were scanned in an Odyssey scanner (LI-COR) using the following parameters: Channel 700, Grid = 8x3, 21.17, Intensity = 5, Offset = 0.
Description Array ID: 0000088678
Data processing ProtoArray signal data was determined with GenePix Pro v5.0.0.49 (Molecular Devices) and then processed following the manufacturer's recommendations using ProtoArray Prospector v5.2 (Invitrogen) with default settings.
 
Submission date May 19, 2020
Last update date Mar 11, 2024
Contact name Emil Karaulanov
Organization name Institute of Molecular Biology
Lab Bioinformatics Core Facility
Street address Ackermannweg 4
City Mainz
ZIP/Postal code 55128
Country Germany
 
Platform ID GPL27459
Series (1)
GSE150859 Analysis of DDX39 and DDX56 interacting proteins

Data table header descriptions
ID_REF
VALUE background-subtracted fluorescence intensity

Data table
ID_REF VALUE
1 129.5
2 492.5
3 2769
4 188
5 301
6 968.5
7 364
8 2979.5
9 1100.5
10 98
11 1232.5
12 109.5
13 106
14 316.5
15 583
16 1142.5
17 274.5
18 409
19 199
20 1108.5

Total number of rows: 9375

Table truncated, full table size 90 Kbytes.




Supplementary file Size Download File type/resource
GSM4559809_DDX39.gpr.gz 1.4 Mb (ftp)(http) GPR
Processed data included within Sample table

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