→ rdfs:label → "Somers Cancer Research"^^xsd:string
→ skos:notation → "9580"^^http://id.southampton.ac.uk/ns/building-code-scheme
→ dcterms:spatial → "POLYGON((-1.43348421183 50.9344557061,-1.43351183822 50.9344320777,-1.43354143792 50.9344084493,-1.43384927485 50.9341684336,-1.43380980858 50.9340167132,-1.43377626225 50.9340229313,-1.43374863586 50.9340104952,-1.43371311621 50.9340129824,-1.43369338307 50.9340241749,-1.43367956988 50.9340440727,-1.43367956988 50.9340614832,-1.43365194349 50.9340490471,-1.43327898721 50.9343325896,-1.43348421183 50.9344557061))"^^xsd:string
← is
http://data.ordnancesurvey.co.uk/ontology/spatialrelations/within of
← http://id.southampton.ac.uk/equipment/E10045,
http://id.southampton.ac.uk/equipment/E10047,
http://id.southampton.ac.uk/equipment/E10048,
http://id.southampton.ac.uk/equipment/E10049,
http://id.southampton.ac.uk/equipment/E10051,
http://id.southampton.ac.uk/equipment/E10730,
http://id.southampton.ac.uk/equipment/E10792,
http://id.southampton.ac.uk/equipment/E10866,
http://id.southampton.ac.uk/equipment/E10871,
http://id.southampton.ac.uk/equipment/E11040,
http://id.southampton.ac.uk/room/9580-C11A
← is
foaf:depicts of
← https://data.southampton.ac.uk/image-archive/buildings/100/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/1000/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/1600/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/1920/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/200/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/220x220/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/240x260/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/300/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/320x198/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/400/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/480x297/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/50/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/600/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/800/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/800x600/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/raw/9580.jpg,
https://data.southampton.ac.uk/image-archive/buildings/100/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/1000/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/1600/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/1920/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/200/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/220x220/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/240x260/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/300/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/320x198/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/400/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/480x297/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/50/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/600/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/800/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/800x600/1473863912_DSC_0210.JPG,
https://data.southampton.ac.uk/image-archive/buildings/raw/1473863912_DSC_0210.JPG
→ rdfs:label → "Southampton General Hospital"^^xsd:string
→ rdfs:label → "University of Southampton"^^xsd:string
← is
oo:formalOrganization of
← http://id.southampton.ac.uk/building/9580,
http://id.southampton.ac.uk/equipment/E10045,
http://id.southampton.ac.uk/equipment/E10047,
http://id.southampton.ac.uk/equipment/E10048,
http://id.southampton.ac.uk/equipment/E10049,
http://id.southampton.ac.uk/equipment/E10051,
http://id.southampton.ac.uk/equipment/E10730,
http://id.southampton.ac.uk/equipment/E10792,
http://id.southampton.ac.uk/equipment/E10866,
http://id.southampton.ac.uk/equipment/E10871,
http://id.southampton.ac.uk/equipment/E11040
→ rdfs:label → "Building 9580 is non-residential"^^xsd:string
→ rdfs:label → "Olympus CKX41 inverted microscope"^^xsd:string
→ dcterms:description → "For High Resolution cell imaging. In fluorescence microscopy, wide variations between localized fluorophore concentrations within the specimen, coupled to differences in extinction coefficient and quantum yield from one fluorochrome to another, significantly influence the emission signal produced for a given quantity of excitation intensity. Considering that many specimens contain only minute quantities of fluorescent material in any particular viewfield, these combined factors produce an average level of fluorescence emission that is four to six orders of magnitude less than the excitation intensity."^^xsd:string
→ skos:notation → "E10045"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:comment → "For High Resolution cell imaging. In fluorescence microscopy, wide variations between localized fluorophore concentrations within the specimen, coupled to differences in extinction coefficient and quantum yield from one fluorochrome to another, significantly influence the emission signal produced for a given quantity of excitation intensity. Considering that many specimens contain only minute quantities of fluorescent material in any particular viewfield, these combined factors produce an average level of fluorescence emission that is four to six orders of magnitude less than the excitation intensity."^^xsd:string
→ dc:description → "For High Resolution cell imaging. In fluorescence microscopy, wide variations between localized fluorophore concentrations within the specimen, coupled to differences in extinction coefficient and quantum yield from one fluorochrome to another, significantly influence the emission signal produced for a given quantity of excitation intensity. Considering that many specimens contain only minute quantities of fluorescent material in any particular viewfield, these combined factors produce an average level of fluorescence emission that is four to six orders of magnitude less than the excitation intensity."^^xsd:string
→ rdfs:label → "Prominance Hplc Upgrade"^^xsd:string
→ dcterms:description → "The modular Prominence HPLC Series generates highly reproducible chromatography while maintaining the flexibility for which Shimadzu HPLC instrumentation is known. The Prominence HPLC can perform many analytical tasks with one piece of high-performance equipment - QA/QC work, Mass Spec front end, multi-dimensional chromatography."^^xsd:string
→ skos:notation → "E10047"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:comment → "The modular Prominence HPLC Series generates highly reproducible chromatography while maintaining the flexibility for which Shimadzu HPLC instrumentation is known. The Prominence HPLC can perform many analytical tasks with one piece of high-performance equipment - QA/QC work, Mass Spec front end, multi-dimensional chromatography."^^xsd:string
→ dc:description → "The modular Prominence HPLC Series generates highly reproducible chromatography while maintaining the flexibility for which Shimadzu HPLC instrumentation is known. The Prominence HPLC can perform many analytical tasks with one piece of high-performance equipment - QA/QC work, Mass Spec front end, multi-dimensional chromatography."^^xsd:string
→ rdfs:label → "Facscanto Laser␣␣488nm and 633nm benchtop 6 colour analysis machine"^^xsd:string
→ dcterms:description → "Used in protein purification. The FACSCanto in the Somers building is a powerful benchtop machine with 488nm and 633 nm lasers allowing six-colour analysis. These 4 analytical instruments play an essential role in research projects over the whole Division and throughout the Faculty of Medicine."^^xsd:string
→ skos:notation → "E10048"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:comment → "Used in protein purification. The FACSCanto in the Somers building is a powerful benchtop machine with 488nm and 633 nm lasers allowing six-colour analysis. These 4 analytical instruments play an essential role in research projects over the whole Division and throughout the Faculty of Medicine."^^xsd:string
→ dc:description → "Used in protein purification. The FACSCanto in the Somers building is a powerful benchtop machine with 488nm and 633 nm lasers allowing six-colour analysis. These 4 analytical instruments play an essential role in research projects over the whole Division and throughout the Faculty of Medicine."^^xsd:string
→ rdfs:label → "Sedna Scientific TTC Cell Counter"^^xsd:string
→ skos:notation → "E10049"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:comment → "Multiple parameter cell counter."^^xsd:string
→ rdfs:label → "Varioskan Flash Inc Bottom Read"^^xsd:string
→ dcterms:description → "Multiple wave length plate reader. Varioskan Flash spectral scanning multimode reader includes fluorescence intensity, time-resolved fluorescence (TRF), photometric, and optional luminometric detection technologies. It is designed for optimization and analysis of various assays, such as binding assays, ADMETox, molecular biology assays, enzyme kinetic studies, ion-channel and cell signalling assays."^^xsd:string
→ skos:notation → "E10051"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:comment → "Multiple wave length plate reader. Varioskan Flash spectral scanning multimode reader includes fluorescence intensity, time-resolved fluorescence (TRF), photometric, and optional luminometric detection technologies. It is designed for optimization and analysis of various assays, such as binding assays, ADMETox, molecular biology assays, enzyme kinetic studies, ion-channel and cell signalling assays."^^xsd:string
→ dc:description → "Multiple wave length plate reader. Varioskan Flash spectral scanning multimode reader includes fluorescence intensity, time-resolved fluorescence (TRF), photometric, and optional luminometric detection technologies. It is designed for optimization and analysis of various assays, such as binding assays, ADMETox, molecular biology assays, enzyme kinetic studies, ion-channel and cell signalling assays."^^xsd:string
→ rdfs:label → "Seahorse XF Extracellular Flux Analyser"^^xsd:string
→ skos:notation → "E10730"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:label → "FACsvantage / FACstation McIntosh - Cell sorter with 488nm, 633nm and UV lasers"^^xsd:string
→ skos:notation → "E10792"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:label → "Thermo Fisher Orbitrap elite dual-pressure linear ion trap mass spectrometer"^^xsd:string
→ skos:notation → "E10866"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ skos:notation → "E10871"^^http://id.southampton.ac.uk/ns/equipment-code-scheme
→ rdfs:label → "Becton Dickinson - Flow Cytometer"^^xsd:string
→ skos:notation → "E11040"^^http://id.southampton.ac.uk/ns/equipment-code-scheme