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Full Moon BioSystems
phosphorylation-specific antibody microarray ![]() Phosphorylation Specific Antibody Microarray, supplied by Full Moon BioSystems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/phosphorylation-specific+antibody+microarrays+fullmoon+biosystems/phosphorylation+specific+antibody+microarrays/pmc05830343-9-7-0 Average 90 stars, based on 1 article reviews
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Image Search Results
Journal: Clinical Proteomics
Article Title: Current applications of antibody microarrays
doi: 10.1186/s12014-018-9184-2
Figure Lengend Snippet: Review of planar antibody microarray technologies and their applications in the field of proteomics. Images were adopted from Servier Medical Art by Servier ( http://www.servier.com/Powerpoint-image-bank ) and modified by the authors under the following terms: CREATIVE COMMONS Attribution 3.0 Unported (CC BY 3.0)
Article Snippet:
Techniques: Microarray, Modification
Journal: Clinical Proteomics
Article Title: Current applications of antibody microarrays
doi: 10.1186/s12014-018-9184-2
Figure Lengend Snippet: Antibody microarray summary
Article Snippet:
Techniques: Microarray, Phospho-proteomics, Infection, Biomarker Discovery, Virus
Journal: The Journal of Biological Chemistry
Article Title: The Chemokine CCL5 Regulates Glucose Uptake and AMP Kinase Signaling in Activated T Cells to Facilitate Chemotaxis
doi: 10.1074/jbc.M112.348946
Figure Lengend Snippet: CCL5 induces phosphorylation of proteins in the AMPK signaling pathway. A, the Full Moon BioSystems AMPK signaling phospho-specific antibody array includes six replicates (vertical columns) of phospho-specific antibodies and their non-phospho pairs, targeted against proteins in the AMPK signaling pathway. Biotinylated protein lysates were added to microscope slide chambers and fluorescence from Cy3-streptavidin was measured with the Axon GenePix 400A microarray scanner. B, the extent of protein phosphorylation (mean fluorescence intensity, MFI) was normalized within each slide and compared between untreated control and cells treated with 10 nm CCL5 for 10 min. The data are represented as fold CCL5-induction relative to untreated controls. Phosphorylated signaling intermediates associated with metabolism are indicated (red arrows).
Article Snippet:
Techniques: Phospho-proteomics, Ab Array, Microscopy, Fluorescence, Microarray, Control
Journal: The Journal of Biological Chemistry
Article Title: The Chemokine CCL5 Regulates Glucose Uptake and AMP Kinase Signaling in Activated T Cells to Facilitate Chemotaxis
doi: 10.1074/jbc.M112.348946
Figure Lengend Snippet: CCL5 activates the energy-sensing kinase AMPK and the downstream substrate GSK-3β resulting in an increased intracellular ATP levels. A, activated PB T cells were either left untreated or treated with 10 nm CCL5 for the indicated times. Cells were harvested and protein lysates resolved by SDS-PAGE and immunoblotted with anti-phospho-AMPKα (Thr-172) or anti-phospho-GSK-3β (Ser-9) antibodies. Membranes were stripped and reprobed for loading. Relative phosphorylation is shown as signal intensity over loading control. Data are representative of two independent experiments. B, activated PB T cells were either treated with dimethyl sulfoxide or 10 μm compound C for 1 h before treatment with 10 nm CCL5 for the indicated times. Intracellular ATP was measured using a bioluminescent assay. Data are representative of two independent experiments. *, p < 0.01; **, p < 0.05. C, activated PB T-cells were pretreated with dimethyl sulfoxide (DMSO; carrier control), oligomycin (1 μm), or 2-deoxy-glucose (10 mm) for 30 min and then stimulated with IL-2 (20 ng/ml) or CCL5 (10 nm) for 30 min. Intracellular ATP levels were then measured using a bioluminescent assay. Data are representative of two independent experiments. *, p < 0.01.
Article Snippet:
Techniques: SDS Page, Phospho-proteomics, Control
Journal: The Journal of Biological Chemistry
Article Title: The Chemokine CCL5 Regulates Glucose Uptake and AMP Kinase Signaling in Activated T Cells to Facilitate Chemotaxis
doi: 10.1074/jbc.M112.348946
Figure Lengend Snippet: Glucose uptake and AMPK signaling are required for efficient CCL5-mediated chemotaxis. A, activated PB T cells were either left untreated or pretreated with 2-DG at the doses indicated for 1 h. A total of 1 × 105 cells in 100 μl of chemotaxis buffer were then placed in the upper chamber of Transwell chambers. CCL5-mediated chemotaxis was measured using 10 nm CCL5. Data are presented as % migration, with the number of migrated cells at 10 nm CCL5 taken as 100%. Data are representative of three independent experiments. B, activated PB T cells were pre-treated with either dimethyl sulfoxide (DMSO; carrier) or different doses of compound C for 1 h. CCL5-mediated chemotaxis was measured as described in A. Data are representative of three independent experiments. *, p < 0.01.
Article Snippet:
Techniques: Chemotaxis Assay, Migration