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high-speed wavelength-switching device lambda dg-4  (Sutter Instrument Company)


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    Sutter Instrument Company high-speed wavelength-switching device lambda dg-4
    High Speed Wavelength Switching Device Lambda Dg 4, supplied by Sutter Instrument Company, 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/high-speed+wavelength-switching+device+lambda+dg-4/lambda+dg+4/pm36979764-76-11-14
    Average 90 stars, based on 1 article reviews
    high-speed wavelength-switching device lambda dg-4 - by Bioz Stars, 2026-11
    90/100 stars

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    other:

    Article Title: Golli myelin basic proteins stimulate oligodendrocyte progenitor cell proliferation and differentiation in remyelinating adult mouse brain.
    Article Snippet: Golli myelin basic proteins are necessary for normal myelination, acting via voltage and store-dependent Ca entry at multiple steps during oligodendrocyte progenitor cell (OPC) development.. To date nothing is known regarding the role of golli proteins in demyelination or remyelination events.. Here the effects of golli ablation and overexpression in myelin loss and recovery were examined using the cuprizone (CPZ) model of demyelination/remyelination.

    Article Title: Development of Cellular Signaling Pathways by Bioceramic Heat Treatment (Sintering) in Osteoblast Cells.
    Article Snippet: For the 340 and 380 nm excitation wavelengths, a high-speed wavelength-switching device (Lambda DG-4, Sutter Instrument, Novato, CA, USA) was used.

    Article Title: Modulation of Canonical Transient Receptor Potential Channel 1 in the Proliferation of Oligodendrocyte Precursor Cells by the Golli Products of the Myelin Basic Protein Gene
    Article Snippet: To load the dye into cells, primary cultures of oligodendrocytes and brain slices were washed in serum and phenol red-free DMEM and incubated for 45 min at 37°C, 5% CO2 in the same media containing a final concentration of 4μM Fura-2 (AM) (TefLabs) plus 0.08% Pluronic F-127 (Molecular Probes), then washed four times in DMEM and stored in DMEM for 0-1 hours before being imaged ( Paz Soldan et al., 2003 ).

    Fluorescence:

    Article Title: Proline substitutions and threonine pseudophosphorylation of the SH3 ligand of 18.5-kDa myelin basic protein decrease its affinity for the Fyn-SH3 domain and alter process development and protein localization in oligodendrocytes.
    Article Snippet: .. The fluorescence of Fura-2 was excited alternatively at wavelengths of 340 nm and 380 nm by means of a high-speed wavelength-switching device (Lambda DG-4; Sutter Instruments, Novato, CA). .. Image analysis software (SlideBook 4.1; Intelligent Imaging Innovations, San Diego, CA) allowed the selection of several regions of interest within the field from which measurements were taken.

    Article Title: Golli myelin basic proteins regulate oligodendroglial progenitor cell migration through voltage-gated Ca ++ influx
    Article Snippet: Dye excitation, image acquisitions and ROI analysis protocols were performed with Image analysis software (SlideBook 4.1, Intelligent Imaging Innovations, San Diego, CA). .. The fluorescence of Fura-2 was excited alternatively at wavelengths of 340 and 380nm by means of a high-speed wavelength-switching device (Lambda DG-4; Sutter Instruments, Novato, CA). .. Calibration of Ca ++ Signals The dye Fura-2 AM (TefLabs, Austin, TX) plus 0.08% Pluronic F-127 (Molecular Probes, Eugene, OR) was incubated with OPCs cultures for 30min at 37°C at a final concentration of 4 μM.

    Article Title: The Circadian Clock Gene Period1 Connects the Molecular Clock to Neural Activity in the Suprachiasmatic Nucleus.
    Article Snippet: A cooled CCD camera (CoolSNAP ES, 1392 1040 pixel format, Photometrics, Tucson, AZ) was added to the fixed-stage microscope (BX50, Olympus) to measure fluorescence. .. The fluorescence of Fura2 was excited alternatively at wavelengths of 357 nm and 380 nm by means of a high-speed wavelength-switching device (Lambda DG-4; Sutter Instruments). .. Image analysis software (MetaFluor, Thermo Fisher Scientific) allowed the selection of several regions of interest within the field from which measurements are taken.

    Article Title: Multiple kinase pathways regulate voltage-dependent Ca ++ influx and migration in oligodendrocyte precursor cells
    Article Snippet: To load the dye into cells, primary cultures of oligodendrocytes and brain slices were washed in serum and phenol red-free DMEM and incubated for 45 min at 37°C, 5% CO2 in the same media containing a final concentration of 4μM Fura-2 (AM) (TefLabs, Austin, TX) plus 0.08% Pluronic F-127 (Molecular Probes, Eugene, OR), then washed four times in DMEM and stored in DMEM for 0-1 hours before being imaged ( Paz Soldan et al., 2003 ). .. The fluorescence of Fura-2 was excited alternatively at wavelengths of 340 and 380 nm by means of a high-speed wavelength-switching device (Lambda DG-4; Sutter Instruments, Novato, CA). .. Image analysis software (SlideBookTM 4.1, Intelligent Imaging Innovations, San Diego, CA) allowed the selection of several “regions of interest” within the field from which measurements were taken.

    Article Title: Modulation of Canonical Transient Receptor Potential Channel 1 in the Proliferation of Oligodendrocyte Precursor Cells by the Golli Products of the Myelin Basic Protein Gene
    Article Snippet: .. The fluorescence of fura-2 was excited alternatively at wavelengths of 340 and 380 nm by means of a high-speed wavelength-switching device (Lambda DG-4; Sutter Instruments). .. The fluorescence of fura-2 was excited alternatively at wavelengths of 340 and 380 nm by means of a high-speed wavelength-switching device (Lambda DG-4; Sutter Instruments).



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