ABSTRACT: The skin of three volunteers has been sampled with PDMS patches across various body sites. The volatiles were desorbed at 200C and analyzed with GC-MS.
Project description:The skin of three volunteers has been sampled with PDMS patches across various body sites. The volatiles were desorbed at 200C and analyzed with GC-MS. Re-submission with mzML files
Project description:GC data for three volunteers. The skin across several body sites was sampled with PDMS patch overnight. The volatiles were desorbed in vial at 200 C.
Project description:Ocean water samples from Guam sampled using PDMS sorbent patch. The sample desorbed at 200C and headspace is injected for GCMS analysis.
Project description:We performed RNA sequencing of islets of Langerhans isolated from RipmiR-141~200c and RipmiR-141~200c Zeb1200M mice to determine the transcriptomic effects of mutating miR-200 binding sites in the endogenous Zeb1 3'UTR of mice in which miR-141~200c is overexpressed under the rat insulin promoter (RIP).
Project description:Skin samples collected from underarm w/ PDMS for 30 seconds. Samples used for optimization of GC headspace methodology wrt desorption time, cryofocusing, and size of PDMS patch (10mL vials were used).
Project description:In the production of seedless table grapes, it is conventional to use plant growth regulators including gibberellins. Little is known about the differences in aroma volatiles between seedless-treated grapes and nontreated (seeded) grapes. Therefore, in this study, the aroma volatile profiles of seedless-treated and nontreated ‘Shine Muscat’ grape berries during ripening were compared using gas chromatography-mass spectrometry. Measurements of volatiles during ripening showed 202 peaks in the seedless-treated and nontreated whole grape berries. According to two-way analysis of variance, the number of volatiles with differences between seedless-treated and nontreated berries and/or between ripening stages was 123, whereas those with no differences between treatments and between ripening stages was 79. Two-way hierarchical clustering analysis for the 123 volatiles showed that seedless-treated berries at the early ripening stages were separated from the other berries, and the seedless-treated and nontreated berries at the post-ripening stage were classified into the same cluster. At the early ripening stage, more lipoxygenase-pathway volatiles were produced in the seedless-treated berries than in the non-treated ones. Linalool compounds increased in both seedless-treated and nontreated berries with ripening. Gene expression profile comparisons using principal component analysis of RNA-sequencing data showed that the seedless-treated berries ripened earlier than the nontreated berries at the early ripening stage. The number of differentially expressed genes in the seedless-treated berries decreased during ripening. Using weighted gene co-expression network analyses, 12 modules and 24 modules were detected in berry skin and flesh, respectively. The correlation analysis revealed that 33 volatiles correlated with four modules in the skin and 50 volatiles correlated with nine modules in the flesh. Most of the volatiles correlated with these modules were those that showed significant differences between treatments and/or ripening stages by two-way analysis of variance. The differences in the aroma volatile profiles between seedless-treated and nontreated berries decreased as harvest was delayed, suggesting that delaying the harvest may make it possible to bring the aroma of seedless-treated ‘Shine Muscat’ berries closer to the original aroma of the seeded berries.
Project description:A total of 63 volunteers were recruited and selected with a stronger than normal underarm malodor, as determined by a trained odor panel. The volunteers were using bacterial sprays and placebo sprays in the underarm to verify the effect on the underarm odor. Odor analysis was done using hedonic value measurement by a trained odor panel, as well as GC/MS analysis. Cleaned and degassed PDMS patches were placed on the underarm skin of the volunteer for 4h and secured in place with a large cotton bandage. After sampling, the bandage was removed, patches placed into 2 mL borosilicate vials using clean tweezers and capped with a crimp camp with silicone septum.
The GC-MS analysis was carried out using the Agilent 7200 GC/QTOF equipped with robotic sampler system.
Project description:MS/MS data were collected from skin swab samples of one volunteer. Samples were collected from psoriasis sites located on elbows, arms, lower back and on the neck hairline. Nearby healthy skin was also sampled as a control.
Project description:Data from skin swabs. Swabs collected from volunteers armpits, chests, upper and lower back. Study aims to reveal an impact of clothing onto the human body and microbiome