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Sample GSM1216149 Query DataSets for GSM1216149
Status Public on Aug 26, 2015
Title Training patient #8 | Vaccine Arm | Day 86 | Training IgG 1-50
Sample type protein
 
Channel 1
Source name Serum
Organism Homo sapiens
Characteristics age at enrollment (years): 65
halabi predicted survival (months): 8.739219713
on-study psa: 3973
gleason #: 9
ellispot: 4.4
tregs: n/a
survival status at last follow-up (1 = alive, 0 = deceased): 0
overall survival (mos): 5.34426229508197
pre-vaccination igg titer for vaccinia: 1250
post-vaccination igg titer for vaccinia: 1250
pre-vaccination igg titer for fowlpox: <50
post-vaccination igg titer for fowlpox: >6250
treatment: Vaccine
timepoint: Post-vaccination
molecule: IgG
Treatment protocol Diluted 1:50
Growth protocol N/A
Extracted molecule protein
Extraction protocol Serum was obtained from peripheral blood samples
Label DyLight 549
Label protocol After serum was incubated on the array, bound anti-glycan antibodies were labeled for 2 hours with a combination of DyLight549 conjugated anti human IgG (Jackson 109-505-008) and DyLight 649 conjugated anti-human IgM (Jackson Immuno, 109-495-043).
 
Channel 2
Source name Serum
Organism Homo sapiens
Characteristics age at enrollment (years): 65
halabi predicted survival (months): 8.739219713
on-study psa: 3973
gleason #: 9
ellispot: 4.4
tregs: n/a
survival status at last follow-up (1 = alive, 0 = deceased): 0
overall survival (mos): 5.34426229508197
pre-vaccination igg titer for vaccinia: 1250
post-vaccination igg titer for vaccinia: 1250
pre-vaccination igg titer for fowlpox: <50
post-vaccination igg titer for fowlpox: >6250
molecule: IgM
Treatment protocol Diluted 1:50
Extracted molecule protein
Extraction protocol Serum was obtained from peripheral blood samples
Label DyLight 649
Label protocol After serum was incubated on the array, bound anti-glycan antibodies were labeled for 2 hours with a combination of DyLight549 conjugated anti human IgG (Jackson 109-505-008) and DyLight 649 conjugated anti-human IgM (Jackson Immuno, 109-495-043).
 
 
Hybridization protocol Arrays were blocked with BSA overnight, and serum samples (diluted 1:50) was incubated on the array for 3 hours at 37 C and gentle agitation (100 RPM).  Slides were then washed with PBS contain 0.05% Tween (PBST).  After washing, bound antibodies were detected with fluorescently labeled secondary antibodies.  Slides were then washed with PBST, spun dry in a centrifuge, and scanned.
Scan protocol Slides were scanned with a Genepix 4000A fluorescence scanner at two gain settings (typically 430 and 520) in order to increase dynamic range.  Signal from ch1 (532 nm) was analyzed to determine the level of bound DyLight 549 conjugated secondary antibody specific for human IgG. Signal from ch2 (635nm) was analyzed to determine the level of bound DyLight 649 secondary antibody specific for human IgM. Scanned images were analyzed with Genepix Pro (v6.0) to determine the fluorescence and background signal for each array component.
Data processing First, median pixel intensity of each feature was background subtracted.  Second, signals for features that were saturated at the high photomultipler tube (PMT) setting were calculated by proportionally scaling the value from the low PMT setting according to a correction factor, which was calculated based on mid-intensity signals measured at the high and low PMT settings.  To account for slide-to-slide variations in array processing, microarray data were normalized by median centering based on a reference serum sample analyzed on each slide.  Additionally, a minimum signal of 150 was set as the floor.  Since array features were printed in duplicate and all samples were analyzed on two slides, pre-processing averaged normalized data from 4 technical replicates.  Final data are reported on a log 2 scale. 
 
Submission date Aug 27, 2013
Last update date Aug 26, 2015
Contact name Christopher Campbell
Organization name NCI
Street address 376 Boyles Street
City Frederick
State/province MD
ZIP/Postal code 21702
Country USA
 
Platform ID GPL16262
Series (2)
GSE50230 Post-vaccination serum anti-glycan IgG antibodies of 28 subjects in a clinical trial of PROSTVAC-VF, a therapeutic cancer vaccine. (Dilution = 1:50)
GSE50410 Anti-glycan humoral responses after vaccination with PROSTVAC-VF

Data table header descriptions
ID_REF
VALUE log 2[average(normalized, background-subtracted median pixel intensity for technical replicates)]

Data table
ID_REF VALUE
2'FucLac 13.43418107
3'SLacNAc 7.22881869
3'Sia-3-FL 11.67243956
6'Slac 10.0284006
Ac-A-Tn(Thr)-S-G - 05 7.22881869
Ac-A-Tn(Thr)-S-G - 08 7.22881869
Ac-A-Tn(Thr)-S-G - 23 8.213922947
Ac-G-V-Tn(Thr)-S-A-G - 04 7.22881869
Ac-G-V-Tn(Thr)-S-A-G - 21 7.22881869
Ac-P-Tn(Thr)-T-G - 05 7.22881869
Ac-P-Tn(Thr)-T-G - 08 7.22881869
Ac-P-Tn(Thr)-T-G - 22 7.22881869
Ac-S-S-S-G 13.40153418
Ac-S-TF(Ser)-S-G - 04 7.22881869
Ac-S-TF(Ser)-S-G - 16 7.22881869
Ac-S-TF(Ser)-S-G - 28 7.22881869
Ac-S-Thr-S-A-G - 18 7.22881869
Ac-S-Tn(Ser)-S-G - 04 7.22881869
Ac-S-Tn(Ser)-S-G - 22 7.22881869
Ac-S-Tn(Ser)-S-G - 33 9.71867371

Total number of rows: 204

Table truncated, full table size 4 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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