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stimulator syntech stimulus controller cs55 v2  (Syntech GmbH)

 
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    Syntech GmbH stimulator syntech stimulus controller cs55 v2
    Odor responses of Keystone-LN in fed and starved larvae. ( A ). Schematic of in-vivo calcium imaging set-up. The odor <t>stimulator</t> consists of 3 air outlets, one for the carrier gas flow and two for the pulse flow. Under no stimulus conditions, airflow from outlets 1 and 3 are constant. When a stimulus is triggered, the airflow from outlet 1 is switched to outlet 2, which puffs air through an odor-containing syringe for 1 s, while carrier flow remains constant. Odor responses are recorded from the neurites of Keystones in the AL (Keystone-gal4; UAS-GCaMP6m) using a spinning disk confocal microscope. ( B ) Representative odor-evoked calcium responses in the neurites of Keystone-LNs to the indicated odors diluted in paraffin oil. ( C ) The top panels show maximum projection images of baseline GCaMP fluorescence in Keystone-LN neurites in the antennal lobe. The bottom heatmaps represent the responses of Keystone-LN neurites to the indicated odors under fed and starved conditions. Each row corresponds to responses from an individual larva. The black bar indicates when the 1-s odor stimulus was applied. ( D ) Box plots showing solvent corrected response amplitudes with min–max normalization (see “ ”) comparing responses to different odors in fed and starved states. Mann–Whitney U -test was used to test differences between fed and starved conditions. No statistically significant differences were found for any of the odors tested.
    Stimulator Syntech Stimulus Controller Cs55 V2, supplied by Syntech GmbH, 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/stimulator+syntech+stimulus+controller+cs55+v2/stimulus+controller+cs+55/pmc09492728-290-1-2
    Average 90 stars, based on 1 article reviews
    stimulator syntech stimulus controller cs55 v2 - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "Internal state affects local neuron function in an early sensory processing center to shape olfactory behavior in Drosophila larvae"

    Article Title: Internal state affects local neuron function in an early sensory processing center to shape olfactory behavior in Drosophila larvae

    Journal: Scientific Reports

    doi: 10.1038/s41598-022-20147-1

    Odor responses of Keystone-LN in fed and starved larvae. ( A ). Schematic of in-vivo calcium imaging set-up. The odor stimulator consists of 3 air outlets, one for the carrier gas flow and two for the pulse flow. Under no stimulus conditions, airflow from outlets 1 and 3 are constant. When a stimulus is triggered, the airflow from outlet 1 is switched to outlet 2, which puffs air through an odor-containing syringe for 1 s, while carrier flow remains constant. Odor responses are recorded from the neurites of Keystones in the AL (Keystone-gal4; UAS-GCaMP6m) using a spinning disk confocal microscope. ( B ) Representative odor-evoked calcium responses in the neurites of Keystone-LNs to the indicated odors diluted in paraffin oil. ( C ) The top panels show maximum projection images of baseline GCaMP fluorescence in Keystone-LN neurites in the antennal lobe. The bottom heatmaps represent the responses of Keystone-LN neurites to the indicated odors under fed and starved conditions. Each row corresponds to responses from an individual larva. The black bar indicates when the 1-s odor stimulus was applied. ( D ) Box plots showing solvent corrected response amplitudes with min–max normalization (see “ ”) comparing responses to different odors in fed and starved states. Mann–Whitney U -test was used to test differences between fed and starved conditions. No statistically significant differences were found for any of the odors tested.
    Figure Legend Snippet: Odor responses of Keystone-LN in fed and starved larvae. ( A ). Schematic of in-vivo calcium imaging set-up. The odor stimulator consists of 3 air outlets, one for the carrier gas flow and two for the pulse flow. Under no stimulus conditions, airflow from outlets 1 and 3 are constant. When a stimulus is triggered, the airflow from outlet 1 is switched to outlet 2, which puffs air through an odor-containing syringe for 1 s, while carrier flow remains constant. Odor responses are recorded from the neurites of Keystones in the AL (Keystone-gal4; UAS-GCaMP6m) using a spinning disk confocal microscope. ( B ) Representative odor-evoked calcium responses in the neurites of Keystone-LNs to the indicated odors diluted in paraffin oil. ( C ) The top panels show maximum projection images of baseline GCaMP fluorescence in Keystone-LN neurites in the antennal lobe. The bottom heatmaps represent the responses of Keystone-LN neurites to the indicated odors under fed and starved conditions. Each row corresponds to responses from an individual larva. The black bar indicates when the 1-s odor stimulus was applied. ( D ) Box plots showing solvent corrected response amplitudes with min–max normalization (see “ ”) comparing responses to different odors in fed and starved states. Mann–Whitney U -test was used to test differences between fed and starved conditions. No statistically significant differences were found for any of the odors tested.

    Techniques Used: In Vivo, Imaging, Microscopy, Fluorescence, Solvent, MANN-WHITNEY



    Similar Products

    stimulator syntech stimulus controller cs55 v2  (Syntech GmbH)
    90
    Syntech GmbH stimulator syntech stimulus controller cs55 v2
    Odor responses of Keystone-LN in fed and starved larvae. ( A ). Schematic of in-vivo calcium imaging set-up. The odor <t>stimulator</t> consists of 3 air outlets, one for the carrier gas flow and two for the pulse flow. Under no stimulus conditions, airflow from outlets 1 and 3 are constant. When a stimulus is triggered, the airflow from outlet 1 is switched to outlet 2, which puffs air through an odor-containing syringe for 1 s, while carrier flow remains constant. Odor responses are recorded from the neurites of Keystones in the AL (Keystone-gal4; UAS-GCaMP6m) using a spinning disk confocal microscope. ( B ) Representative odor-evoked calcium responses in the neurites of Keystone-LNs to the indicated odors diluted in paraffin oil. ( C ) The top panels show maximum projection images of baseline GCaMP fluorescence in Keystone-LN neurites in the antennal lobe. The bottom heatmaps represent the responses of Keystone-LN neurites to the indicated odors under fed and starved conditions. Each row corresponds to responses from an individual larva. The black bar indicates when the 1-s odor stimulus was applied. ( D ) Box plots showing solvent corrected response amplitudes with min–max normalization (see “ ”) comparing responses to different odors in fed and starved states. Mann–Whitney U -test was used to test differences between fed and starved conditions. No statistically significant differences were found for any of the odors tested.
    Stimulator Syntech Stimulus Controller Cs55 V2, supplied by Syntech GmbH, 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/stimulator+syntech+stimulus+controller+cs55+v2/stimulus+controller+cs+55/pmc09492728-290-1-2
    Average 90 stars, based on 1 article reviews
    stimulator syntech stimulus controller cs55 v2 - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Odor responses of Keystone-LN in fed and starved larvae. ( A ). Schematic of in-vivo calcium imaging set-up. The odor stimulator consists of 3 air outlets, one for the carrier gas flow and two for the pulse flow. Under no stimulus conditions, airflow from outlets 1 and 3 are constant. When a stimulus is triggered, the airflow from outlet 1 is switched to outlet 2, which puffs air through an odor-containing syringe for 1 s, while carrier flow remains constant. Odor responses are recorded from the neurites of Keystones in the AL (Keystone-gal4; UAS-GCaMP6m) using a spinning disk confocal microscope. ( B ) Representative odor-evoked calcium responses in the neurites of Keystone-LNs to the indicated odors diluted in paraffin oil. ( C ) The top panels show maximum projection images of baseline GCaMP fluorescence in Keystone-LN neurites in the antennal lobe. The bottom heatmaps represent the responses of Keystone-LN neurites to the indicated odors under fed and starved conditions. Each row corresponds to responses from an individual larva. The black bar indicates when the 1-s odor stimulus was applied. ( D ) Box plots showing solvent corrected response amplitudes with min–max normalization (see “ ”) comparing responses to different odors in fed and starved states. Mann–Whitney U -test was used to test differences between fed and starved conditions. No statistically significant differences were found for any of the odors tested.

    Journal: Scientific Reports

    Article Title: Internal state affects local neuron function in an early sensory processing center to shape olfactory behavior in Drosophila larvae

    doi: 10.1038/s41598-022-20147-1

    Figure Lengend Snippet: Odor responses of Keystone-LN in fed and starved larvae. ( A ). Schematic of in-vivo calcium imaging set-up. The odor stimulator consists of 3 air outlets, one for the carrier gas flow and two for the pulse flow. Under no stimulus conditions, airflow from outlets 1 and 3 are constant. When a stimulus is triggered, the airflow from outlet 1 is switched to outlet 2, which puffs air through an odor-containing syringe for 1 s, while carrier flow remains constant. Odor responses are recorded from the neurites of Keystones in the AL (Keystone-gal4; UAS-GCaMP6m) using a spinning disk confocal microscope. ( B ) Representative odor-evoked calcium responses in the neurites of Keystone-LNs to the indicated odors diluted in paraffin oil. ( C ) The top panels show maximum projection images of baseline GCaMP fluorescence in Keystone-LN neurites in the antennal lobe. The bottom heatmaps represent the responses of Keystone-LN neurites to the indicated odors under fed and starved conditions. Each row corresponds to responses from an individual larva. The black bar indicates when the 1-s odor stimulus was applied. ( D ) Box plots showing solvent corrected response amplitudes with min–max normalization (see “ ”) comparing responses to different odors in fed and starved states. Mann–Whitney U -test was used to test differences between fed and starved conditions. No statistically significant differences were found for any of the odors tested.

    Article Snippet: A stimulator (Syntech Stimulus Controller CS55 V2) was used to couple the odor stimulus delivery with imaging.

    Techniques: In Vivo, Imaging, Microscopy, Fluorescence, Solvent, MANN-WHITNEY