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This is an extract of aphid proteins. SDS-PAGE followed by Coomassee staining, trypsin in-gel digestion and RP-LC MS/MS
ORGANISM(S): Buchnera aphidicola subsp. Acyrthosiphon pisum (Acyrthosiphon pisum symbiotic bacterium) Acyrthosiphon pisum (Pea aphid) 
2013-07-02 | PRD000326 | Pride
Recurrent point mutations in SPOP define a distinct molecular subclass of prostate cancer. Here, we describe the first mouse model showing that mutant SPOP drives prostate tumorigenesis in vivo. Conditional expression of mutant SPOP in the prostate dramatically altered phenotypes in the setting of P...
ORGANISM(S): Mus musculus (Mouse) 
2017-03-20 | PXD005309 | Pride
We have examined the transcriptional events in mouse bone marrow derived macrophages (MBDM) with interferon-gamma (Ifng)at 2, 4 & 8 h following treatment or pre-treatment (0 h).
ORGANISM(S): Mus musculus 
Publication title: Distinct DNA methylation patterns characterize differentiated human embryonic stem cells and developing human fetal liver To investigate the role of DNA methylation during human development, we developed Methyl-seq, a method that assays DNA methylation at more than 90,000 regions...
ORGANISM(S): Homo sapiens 
lncRNA interactome study, MCF7 cells, proteomics Velos Pro
ORGANISM(S): Homo sapiens (Human) 
2016-10-05 | PXD002421 | Pride
The most widely-used method for detecting and measuring genome-wide protein-DNA interactions is chromatin immunoprecipitation on tiling microarrays, commonly known as ChIP-chip. Many tiling array platforms, amplification methods, and analysis algorithms exist for ChIP-chip, but a rigorous assessment...
ORGANISM(S): Homo sapiens 
Spinal muscular atrophy (SMA) is a neurodegenerative disease caused by the absence of a functional Survival of Motor Neuron 1 gene (SMN1). The nearly identical paralog, SMN2, cannot compensate for the loss of SMN1 because exon 7 is aberrantly skipped from most SMN2 transcripts, a process mediated by...
ORGANISM(S): Homo sapiens (Human) 
2024-05-23 | PXD033055 | Pride
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