Boana sibleszi
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA1169309 | ENA |
REPOSITORIES: ENA
Similar Datasets
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Project description:Samples were obtained from the dorsal skin of frogs after a mild electrical stimuli. They were freeze-dried and resuspended in water: acetonitrile (7:3) with 0.1% (v/v) trifluoroacetic acid (TFA). The aim of the analyses was to identified secondary metabolites in particular from the Boana pulchella group. After isolation and characterization of two novel macrocyclic acylcarnitines (MACH) by a combination of LC-MS/MS, RMN and GC/MS we also putatively identified other substances from the same series.
2023-07-22 | MSV000092499 | MassIVE
Project description:Samples were obtained from the dorsal skin of frogs after a mild electrical stimuli. They were freeze-dried and resuspended in water: acetonitrile (7:3) with 0.1% (v/v) trifluoroacetic acid (TFA). The aim of the analyses was to identified secondary metabolites in particular from the Boana pulchella group. After isolation and characterization of two novel macrocyclic acylcarnitines (MACH) by a combination of LC-MS/MS, RMN and GC/MS we also putatively identified other substances from the same series.
2023-07-22 | MSV000092499 | GNPS
Project description:modENCODE_submission_5986 This submission comes from a modENCODE project of Jason Lieb. For full list of modENCODE projects, see http://www.genome.gov/26524648 Project Goal: The focus of our analysis will be elements that specify nucleosome positioning and occupancy, control domains of gene expression, induce repression of the X chromosome, guide mitotic segregation and genome duplication, govern homolog pairing and recombination during meiosis, and organize chromosome positioning within the nucleus. Our 126 strategically selected targets include RNA polymerase II isoforms, dosage-compensation proteins, centromere components, homolog-pairing facilitators, recombination markers, and nuclear-envelope constituents. We will integrate information generated with existing knowledge on the biology of the targets and perform ChIP-seq analysis on mutant and RNAi extracts lacking selected target proteins. For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODEDataReleasePolicyFinal2008.pdf EXPERIMENT TYPE: CHIP-seq. BIOLOGICAL SOURCE: Strain: N2; Developmental Stage: L3 Larva; Genotype: wild type; Sex: mixed Male and Hermaphrodite population; EXPERIMENTAL FACTORS: Developmental Stage L3 Larva; temp (temperature) 20 degree celsius; Strain N2; Antibody NURF-1 SDQ3525 (target is NURF-1)
2013-08-28 | E-GEOD-50296 | biostudies-arrayexpress
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2014-05-17 | E-GEOD-57762 | biostudies-arrayexpress
Project description:This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
2015-11-24 | E-GEOD-75306 | biostudies-arrayexpress