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precision isoflurane vaporizer vapomatic 2  (A M BICKFORD INC)

 
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    A M BICKFORD INC precision isoflurane vaporizer vapomatic 2
    Precision Isoflurane Vaporizer Vapomatic 2, supplied by A M BICKFORD 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/vapomatic+vaporizer/pmc11707623-67-5-10?v=A+M+BICKFORD+INC
    Average 90 stars, based on 1 article reviews
    precision isoflurane vaporizer vapomatic 2 - by Bioz Stars, 2026-08
    90/100 stars

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    (A) Image of detected (red and blue encircled) neurons and astrocytes in the awake mouse. Black traces (right) are the neuropil contamination-corrected ΔF/F calcium time series of the red-encircled neurons in the image (left). Vertical lines above the calcium time series indicate times when visual stimuli (gratings) were presented, each movement direction in a different color. The blue trace represents the evolution of the mean correlation between all pairs of displayed neurons (calculated over a sliding two-second window). The red trace shows animal movement, measured from treadmill motion. The green traces indicate the (corrected) horizontal (x) and vertical (y) image displacement, which was highly correlated with animal motion. Respective scale bars are located on the right, grey horizontal lines represent the horizontal zero axis. (B) Idem as in A, but recorded 45 to 70 minutes later under anesthesia (1.0% <t>isoflurane</t> in O2). Note the difference in scaling of the ΔF/F signals with (A).
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    (A) Image of detected (red and blue encircled) neurons and astrocytes in the awake mouse. Black traces (right) are the neuropil contamination-corrected ΔF/F calcium time series of the red-encircled neurons in the image (left). Vertical lines above the calcium time series indicate times when visual stimuli (gratings) were presented, each movement direction in a different color. The blue trace represents the evolution of the mean correlation between all pairs of displayed neurons (calculated over a sliding two-second window). The red trace shows animal movement, measured from treadmill motion. The green traces indicate the (corrected) horizontal (x) and vertical (y) image displacement, which was highly correlated with animal motion. Respective scale bars are located on the right, grey horizontal lines represent the horizontal zero axis. (B) Idem as in A, but recorded 45 to 70 minutes later under anesthesia (1.0% <t>isoflurane</t> in O2). Note the difference in scaling of the ΔF/F signals with (A).
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    (A) Image of detected (red and blue encircled) neurons and astrocytes in the awake mouse. Black traces (right) are the neuropil contamination-corrected ΔF/F calcium time series of the red-encircled neurons in the image (left). Vertical lines above the calcium time series indicate times when visual stimuli (gratings) were presented, each movement direction in a different color. The blue trace represents the evolution of the mean correlation between all pairs of displayed neurons (calculated over a sliding two-second window). The red trace shows animal movement, measured from treadmill motion. The green traces indicate the (corrected) horizontal (x) and vertical (y) image displacement, which was highly correlated with animal motion. Respective scale bars are located on the right, grey horizontal lines represent the horizontal zero axis. (B) Idem as in A, but recorded 45 to 70 minutes later under anesthesia (1.0% <t>isoflurane</t> in O2). Note the difference in scaling of the ΔF/F signals with (A).
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    (A) Image of detected (red and blue encircled) neurons and astrocytes in the awake mouse. Black traces (right) are the neuropil contamination-corrected ΔF/F calcium time series of the red-encircled neurons in the image (left). Vertical lines above the calcium time series indicate times when visual stimuli (gratings) were presented, each movement direction in a different color. The blue trace represents the evolution of the mean correlation between all pairs of displayed neurons (calculated over a sliding two-second window). The red trace shows animal movement, measured from treadmill motion. The green traces indicate the (corrected) horizontal (x) and vertical (y) image displacement, which was highly correlated with animal motion. Respective scale bars are located on the right, grey horizontal lines represent the horizontal zero axis. (B) Idem as in A, but recorded 45 to 70 minutes later under anesthesia (1.0% <t>isoflurane</t> in O2). Note the difference in scaling of the ΔF/F signals with (A).
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    Image Search Results


    (A) Image of detected (red and blue encircled) neurons and astrocytes in the awake mouse. Black traces (right) are the neuropil contamination-corrected ΔF/F calcium time series of the red-encircled neurons in the image (left). Vertical lines above the calcium time series indicate times when visual stimuli (gratings) were presented, each movement direction in a different color. The blue trace represents the evolution of the mean correlation between all pairs of displayed neurons (calculated over a sliding two-second window). The red trace shows animal movement, measured from treadmill motion. The green traces indicate the (corrected) horizontal (x) and vertical (y) image displacement, which was highly correlated with animal motion. Respective scale bars are located on the right, grey horizontal lines represent the horizontal zero axis. (B) Idem as in A, but recorded 45 to 70 minutes later under anesthesia (1.0% isoflurane in O2). Note the difference in scaling of the ΔF/F signals with (A).

    Journal: PLoS ONE

    Article Title: Effects of Isoflurane Anesthesia on Ensemble Patterns of Ca 2+ Activity in Mouse V1: Reduced Direction Selectivity Independent of Increased Correlations in Cellular Activity

    doi: 10.1371/journal.pone.0118277

    Figure Lengend Snippet: (A) Image of detected (red and blue encircled) neurons and astrocytes in the awake mouse. Black traces (right) are the neuropil contamination-corrected ΔF/F calcium time series of the red-encircled neurons in the image (left). Vertical lines above the calcium time series indicate times when visual stimuli (gratings) were presented, each movement direction in a different color. The blue trace represents the evolution of the mean correlation between all pairs of displayed neurons (calculated over a sliding two-second window). The red trace shows animal movement, measured from treadmill motion. The green traces indicate the (corrected) horizontal (x) and vertical (y) image displacement, which was highly correlated with animal motion. Respective scale bars are located on the right, grey horizontal lines represent the horizontal zero axis. (B) Idem as in A, but recorded 45 to 70 minutes later under anesthesia (1.0% isoflurane in O2). Note the difference in scaling of the ΔF/F signals with (A).

    Article Snippet: To ensure delivery of a stable concentration of isoflurane, we used the calibrated, commercially available, Vapomatic isoflurane vaporizer (A.M. Bickford, Inc., NY, USA).

    Techniques: