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blue light stimulation pe-100  (CoolLED Inc)

 
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    CoolLED Inc blue light stimulation pe-100
    Blue Light Stimulation Pe 100, supplied by CoolLED Inc, 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/blue+light+stimulation/pe+100/pmc11078648__mmc2-73-21-23
    Average 90 stars, based on 1 article reviews
    blue light stimulation pe-100 - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Activation Assay:

    Article Title: Optimized design and in vivo application of optogenetically functionalized Drosophila dopamine receptors
    Article Snippet: The soma, as well as the medial lobe of the mushroom body, were live imaged using a Zeiss LSM 780 2-photon microscope and a 25x/NA1.0 water immersion objective. .. For activation of the optoDop1R2 V2 , larvae were subjected to 10s blue light stimulation (470 nm, 720 μW/cm2, CoolLED) twice with an interval of 30s between each pulse. ..

    Article Title: Optimized design and in vivo application of optogenetically functionalized Drosophila dopamine receptors.
    Article Snippet: The soma, aswell as themedial lobeof themushroom body, were live imaged using a Zeiss LSM 780 2-photon microscope and a 25x/NA1.0 water immersion objective. .. For activation of the optoDop1R2V2, larvae were subjected to 10s blue light stimulation (470 nm, 720 μW/cm2, CoolLED) twicewith an interval of 30s between each pulse. ..



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    Synaptic linkage analysis between the PL-mPFC and the NAc core. ( A ) The schematic diagram of the electrophysiological experimental design. ( B ) The schematic representation of the viral injection site in the PL-mPFC (left) and PL-NAc virus projection (right) (scale bar: 1000 μm). ( C ) Action potentials were recorded in neurons expressing ChR2-eYFP in the PL-mPFC in current-clamp mode (blue light: 465 nm, 43.7 mW, 5 ms duration) at 5 Hz in order to identify the virus function (blue vertical lines represent light <t>stimulation</t> pulses). ( D ) The eEPSC was recorded in each group. The eEPSC was completely blocked by TTX (1 μM) and recovered by consequent 4-AP (100 μM) (ACSF vs TTX: P < 0.01; TTX vs TTX + 4-AP: P < 0.01). ( E ) The typical eEPSC trajectory diagrams of three groups. The colors displayed are as follows: ACSF group in black, TTX group in red, and TTX + 4-AP group in blue. ** P < 0.01.
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    Synaptic linkage analysis between the PL-mPFC and the NAc core. ( A ) The schematic diagram of the electrophysiological experimental design. ( B ) The schematic representation of the viral injection site in the PL-mPFC (left) and PL-NAc virus projection (right) (scale bar: 1000 μm). ( C ) Action potentials were recorded in neurons expressing ChR2-eYFP in the PL-mPFC in current-clamp mode (blue light: 465 nm, 43.7 mW, 5 ms duration) at 5 Hz in order to identify the virus function (blue vertical lines represent light stimulation pulses). ( D ) The eEPSC was recorded in each group. The eEPSC was completely blocked by TTX (1 μM) and recovered by consequent 4-AP (100 μM) (ACSF vs TTX: P < 0.01; TTX vs TTX + 4-AP: P < 0.01). ( E ) The typical eEPSC trajectory diagrams of three groups. The colors displayed are as follows: ACSF group in black, TTX group in red, and TTX + 4-AP group in blue. ** P < 0.01.

    Journal: Journal of Pain Research

    Article Title: Restoration of the Activity of the Prefrontal Cortex to the Nucleus Accumbens Core Pathway Relieves Fentanyl-Induced Hyperalgesia in Male Rats

    doi: 10.2147/JPR.S442765

    Figure Lengend Snippet: Synaptic linkage analysis between the PL-mPFC and the NAc core. ( A ) The schematic diagram of the electrophysiological experimental design. ( B ) The schematic representation of the viral injection site in the PL-mPFC (left) and PL-NAc virus projection (right) (scale bar: 1000 μm). ( C ) Action potentials were recorded in neurons expressing ChR2-eYFP in the PL-mPFC in current-clamp mode (blue light: 465 nm, 43.7 mW, 5 ms duration) at 5 Hz in order to identify the virus function (blue vertical lines represent light stimulation pulses). ( D ) The eEPSC was recorded in each group. The eEPSC was completely blocked by TTX (1 μM) and recovered by consequent 4-AP (100 μM) (ACSF vs TTX: P < 0.01; TTX vs TTX + 4-AP: P < 0.01). ( E ) The typical eEPSC trajectory diagrams of three groups. The colors displayed are as follows: ACSF group in black, TTX group in red, and TTX + 4-AP group in blue. ** P < 0.01.

    Article Snippet: To record light-evoked excitatory postsynaptic currents (eEPSC) and light-excited inhibitory postsynaptic currents (eIPSC), 5 mM QX-314 (MCE, New Jersey, USA) was added to the internal solution, and blue light stimulation was provided using a 40 × water-immersion objective lens (Eclipse FN1, Nikon) for 2 ms to activate channelrhodopsin-2 (ChR2) (pE-300 white, CoolLED co.,ltd, Andover, UK). eEPSC and eIPSC were recorded in voltage-clamp mode at −70 mV and −30 mV, respectively.

    Techniques: Injection, Virus, Expressing