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Sample GSM5639117 Query DataSets for GSM5639117
Status Public on Sep 26, 2022
Title s63
Sample type protein
 
Source name Amniotic fluid
Organism Homo sapiens
Characteristics gender: female
diagnosis: sonographic short cervix
tissue: Amniotic fluid
gaamniocentesis: 18.3
gadelivery: 20.3
cervical length: 5
deliverywithin2weeks: 1
Extracted molecule protein
Extraction protocol none
Label Cy3
Label protocol The amniotic fluid samples were diluted and then incubated with the respective SOMAmer mixes pre-immobilized onto streptavidin-coated beads. The beads were washed in order to remove all non-specifically bound proteins and other matrix constituents. Proteins that remained specifically bound to their cognate SOMAmer reagents were tagged using an NHS-biotin reagent. After the labeling reaction, the beads were exposed to an anionic competitor solution that prevents non-specific interactions from reforming after disruption. Using this approach, pure cognate-SOMAmer complexes and unbound (free) SOMAmer reagents are released from the streptavidin beads using ultraviolet light that cleaves the photo-cleavable linker used to quantitate protein. The photo-cleavage eluate, which contains all SOMAmer reagents (some bound to a biotin-labeled protein and some free), was separated from the beads and then incubated with a second streptavidin-coated bead that binds the biotin-labeled proteins and the biotin-labeled protein-SOMAmer complexes. The free SOMAmer reagents were then removed during subsequent washing steps. In the final elution step, protein-bound SOMAmer reagents were released from their cognate proteins using denaturing conditions.
 
Hybridization protocol These SOMAmer reagents were then quantified by hybridization to custom DNA microarrays.
Scan protocol The Cyanine-3 signal from the SOMAmer reagent was detected on microarrays. More details on all protocols are described in Gold L, et al. PLoS One.
Data processing The raw protein abundance data consisted of relative fluorescence units quantified by using the SOMAmer (Slow Off-rate Modified Aptamers) platform and its reagents.
 
Submission date Oct 19, 2021
Last update date Sep 26, 2022
Contact name Adi Tarca
E-mail(s) atarca@med.wayne.edu
Phone 313-577-5305
Organization name Wayne State University
Department Perinatology Research Branch (NIH/NICHD)
Lab Bioinformatics and Computational Biology Unit
Street address 3990 John R.
City Detroit
State/province Michigan
ZIP/Postal code 48201
Country USA
 
Platform ID GPL23119
Series (1)
GSE186135 The amniotic fluid proteome improves prediction of imminent delivery relative to quantitative cervical length: a cross-sectional study in women with a short cervix

Data table header descriptions
ID_REF
VALUE Relative fluorescence units (RFU)

Data table
ID_REF VALUE
SL019100 21.5
SL007136 9.8
SL001731 272.6
SL019096 15.6
SL005173 98.8
SL007221 41.2
SL007108 58.2
SL000455 38.1
SL003755 44.7
SL014684 15.4
SL002565 17.4
SL004097 36.3
SL004101 25.2
SL005184 59.8
SL001728 109.9
SL001716 10.4
SL004396 19.3
SL007229 25.6
SL017128 280.4
SL001791 222.6

Total number of rows: 1310

Table truncated, full table size 18 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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