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grin lens (basic fluorescence snap-in microscopy system – deep brain)  (Doric Lenses Inc)

 
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    Structured Review

    Doric Lenses Inc grin lens (basic fluorescence snap-in microscopy system – deep brain)
    (A) Schematic of deep brain calcium imaging. (B) Representative images of <t>GRIN</t> lens placement and field of view from Slc32a1 Cre and Lepr Cre mice. Scale bars: top, 500 μm; bottom, 100 μm. (C) Slc32a1 Cre (n = 9) and Lepr Cre (n = 8) mice used for functional imaging experiments on average performed most post-CS licks following CS + trials. (D) Normalized Ca 2+ traces of individual <t>LH</t> <t>VGAT</t> neurons on CS + or CS − trials. Vertical dashed lines indicate the beginning of the CS and outcome epochs. Horizontal dashed lines indicate groupings of neurons according to the epoch of maximal activity. (E–G) Normalized traces of CS + (orange) and CS − (gray) trials of (E) pre-responsive, (F) cue-responsive, and (G) reward-responsive LH VGAT neurons. (H–K) Similar to (E)–(G), except for LH LEPR neurons. (L) LH LEPR activity during the CS epoch discriminated trial types whereas LH VGAT activity did not. *p = 0.017, ****p < 0.0001. (M) Maximal activity of individual LH VGAT neurons on CS + and CS − trials, without matching the sampled time bin. Dashed lines indicate sample CS + /CS − ratios. The LH VGAT centroid ratio was 1.26, indicating slight preference for CS + trials. (N) Similar to (M), but for LH LEPR neurons; the centroid ratio was 2.00, indicating large preference for CS + trials. (O) CS + selectivity index (CS + response/ΣCS responses) was higher for LH LEPR than LH VGAT neurons (p = 0.0034). Data represented as means ± SEMs. See also for full statistics.
    Grin Lens (Basic Fluorescence Snap In Microscopy System – Deep Brain), supplied by Doric Lenses 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/basic+fluorescence+snap-in+microscopy+system+%E2%80%93+deep+brain/grin+lens++basic+fluorescence+snap+in+microscopy+system+++deep+brain+/pmc08423025-289-23-33
    Average 90 stars, based on 1 article reviews
    grin lens (basic fluorescence snap-in microscopy system – deep brain) - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Lateral hypothalamic LEPR neurons drive appetitive but not consummatory behaviors"

    Article Title: Lateral hypothalamic LEPR neurons drive appetitive but not consummatory behaviors

    Journal: Cell reports

    doi: 10.1016/j.celrep.2021.109615

    (A) Schematic of deep brain calcium imaging. (B) Representative images of GRIN lens placement and field of view from Slc32a1 Cre and Lepr Cre mice. Scale bars: top, 500 μm; bottom, 100 μm. (C) Slc32a1 Cre (n = 9) and Lepr Cre (n = 8) mice used for functional imaging experiments on average performed most post-CS licks following CS + trials. (D) Normalized Ca 2+ traces of individual LH VGAT neurons on CS + or CS − trials. Vertical dashed lines indicate the beginning of the CS and outcome epochs. Horizontal dashed lines indicate groupings of neurons according to the epoch of maximal activity. (E–G) Normalized traces of CS + (orange) and CS − (gray) trials of (E) pre-responsive, (F) cue-responsive, and (G) reward-responsive LH VGAT neurons. (H–K) Similar to (E)–(G), except for LH LEPR neurons. (L) LH LEPR activity during the CS epoch discriminated trial types whereas LH VGAT activity did not. *p = 0.017, ****p < 0.0001. (M) Maximal activity of individual LH VGAT neurons on CS + and CS − trials, without matching the sampled time bin. Dashed lines indicate sample CS + /CS − ratios. The LH VGAT centroid ratio was 1.26, indicating slight preference for CS + trials. (N) Similar to (M), but for LH LEPR neurons; the centroid ratio was 2.00, indicating large preference for CS + trials. (O) CS + selectivity index (CS + response/ΣCS responses) was higher for LH LEPR than LH VGAT neurons (p = 0.0034). Data represented as means ± SEMs. See also for full statistics.
    Figure Legend Snippet: (A) Schematic of deep brain calcium imaging. (B) Representative images of GRIN lens placement and field of view from Slc32a1 Cre and Lepr Cre mice. Scale bars: top, 500 μm; bottom, 100 μm. (C) Slc32a1 Cre (n = 9) and Lepr Cre (n = 8) mice used for functional imaging experiments on average performed most post-CS licks following CS + trials. (D) Normalized Ca 2+ traces of individual LH VGAT neurons on CS + or CS − trials. Vertical dashed lines indicate the beginning of the CS and outcome epochs. Horizontal dashed lines indicate groupings of neurons according to the epoch of maximal activity. (E–G) Normalized traces of CS + (orange) and CS − (gray) trials of (E) pre-responsive, (F) cue-responsive, and (G) reward-responsive LH VGAT neurons. (H–K) Similar to (E)–(G), except for LH LEPR neurons. (L) LH LEPR activity during the CS epoch discriminated trial types whereas LH VGAT activity did not. *p = 0.017, ****p < 0.0001. (M) Maximal activity of individual LH VGAT neurons on CS + and CS − trials, without matching the sampled time bin. Dashed lines indicate sample CS + /CS − ratios. The LH VGAT centroid ratio was 1.26, indicating slight preference for CS + trials. (N) Similar to (M), but for LH LEPR neurons; the centroid ratio was 2.00, indicating large preference for CS + trials. (O) CS + selectivity index (CS + response/ΣCS responses) was higher for LH LEPR than LH VGAT neurons (p = 0.0034). Data represented as means ± SEMs. See also for full statistics.

    Techniques Used: Imaging, Functional Assay, Activity Assay

    Related Articles

    Fluorescence:

    Article Title: An excitatory lateral hypothalamic circuit orchestrating pain behaviors in mice
    Article Snippet: Other , Snap-in Imaging Cannula Model L-V , Doric Lenses Inc , , GRIN lenses. .. Other , Basic Fluorescence Snap-In Microscopy System – Deep Brain , Doric Lenses Inc , , In vivo imaging system. ..

    Microscopy:

    Article Title: An excitatory lateral hypothalamic circuit orchestrating pain behaviors in mice
    Article Snippet: Other , Snap-in Imaging Cannula Model L-V , Doric Lenses Inc , , GRIN lenses. .. Other , Basic Fluorescence Snap-In Microscopy System – Deep Brain , Doric Lenses Inc , , In vivo imaging system. ..

    In Vivo Imaging:

    Article Title: An excitatory lateral hypothalamic circuit orchestrating pain behaviors in mice
    Article Snippet: Other , Snap-in Imaging Cannula Model L-V , Doric Lenses Inc , , GRIN lenses. .. Other , Basic Fluorescence Snap-In Microscopy System – Deep Brain , Doric Lenses Inc , , In vivo imaging system. ..



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    Doric Lenses Inc grin lens (basic fluorescence snap-in microscopy system – deep brain)
    (A) Schematic of deep brain calcium imaging. (B) Representative images of <t>GRIN</t> lens placement and field of view from Slc32a1 Cre and Lepr Cre mice. Scale bars: top, 500 μm; bottom, 100 μm. (C) Slc32a1 Cre (n = 9) and Lepr Cre (n = 8) mice used for functional imaging experiments on average performed most post-CS licks following CS + trials. (D) Normalized Ca 2+ traces of individual <t>LH</t> <t>VGAT</t> neurons on CS + or CS − trials. Vertical dashed lines indicate the beginning of the CS and outcome epochs. Horizontal dashed lines indicate groupings of neurons according to the epoch of maximal activity. (E–G) Normalized traces of CS + (orange) and CS − (gray) trials of (E) pre-responsive, (F) cue-responsive, and (G) reward-responsive LH VGAT neurons. (H–K) Similar to (E)–(G), except for LH LEPR neurons. (L) LH LEPR activity during the CS epoch discriminated trial types whereas LH VGAT activity did not. *p = 0.017, ****p < 0.0001. (M) Maximal activity of individual LH VGAT neurons on CS + and CS − trials, without matching the sampled time bin. Dashed lines indicate sample CS + /CS − ratios. The LH VGAT centroid ratio was 1.26, indicating slight preference for CS + trials. (N) Similar to (M), but for LH LEPR neurons; the centroid ratio was 2.00, indicating large preference for CS + trials. (O) CS + selectivity index (CS + response/ΣCS responses) was higher for LH LEPR than LH VGAT neurons (p = 0.0034). Data represented as means ± SEMs. See also for full statistics.
    Grin Lens (Basic Fluorescence Snap In Microscopy System – Deep Brain), supplied by Doric Lenses 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/basic+fluorescence+snap-in+microscopy+system+%E2%80%93+deep+brain/grin+lens++basic+fluorescence+snap+in+microscopy+system+++deep+brain+/pmc08423025-289-23-33
    Average 90 stars, based on 1 article reviews
    grin lens (basic fluorescence snap-in microscopy system – deep brain) - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

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    Doric Lenses Inc basic fluorescence snap-in microscopy system - deep brain, doric lenses
    KEY RESOURCES TABLE
    Basic Fluorescence Snap In Microscopy System Deep Brain, Doric Lenses, supplied by Doric Lenses 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/basic+fluorescence+snap-in+microscopy+system+%E2%80%93+deep+brain/basic+fluorescence+snap+in+microscopy+system+++deep+brain++doric+lenses/pmc08423025-32-0-9
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    basic fluorescence snap-in microscopy system - deep brain, doric lenses - by Bioz Stars, 2026-10
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    Doric Lenses Inc basic fluorescence snap-in microscopy system – deep brain

    Basic Fluorescence Snap In Microscopy System – Deep Brain, supplied by Doric Lenses 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/basic+fluorescence+snap-in+microscopy+system+%E2%80%93+deep+brain/basic+fluorescence+snap+in+microscopy+system+++deep+brain/pmc08159376-33-2-11
    Average 90 stars, based on 1 article reviews
    basic fluorescence snap-in microscopy system – deep brain - by Bioz Stars, 2026-10
    90/100 stars
      Buy from Supplier

    Image Search Results


    (A) Schematic of deep brain calcium imaging. (B) Representative images of GRIN lens placement and field of view from Slc32a1 Cre and Lepr Cre mice. Scale bars: top, 500 μm; bottom, 100 μm. (C) Slc32a1 Cre (n = 9) and Lepr Cre (n = 8) mice used for functional imaging experiments on average performed most post-CS licks following CS + trials. (D) Normalized Ca 2+ traces of individual LH VGAT neurons on CS + or CS − trials. Vertical dashed lines indicate the beginning of the CS and outcome epochs. Horizontal dashed lines indicate groupings of neurons according to the epoch of maximal activity. (E–G) Normalized traces of CS + (orange) and CS − (gray) trials of (E) pre-responsive, (F) cue-responsive, and (G) reward-responsive LH VGAT neurons. (H–K) Similar to (E)–(G), except for LH LEPR neurons. (L) LH LEPR activity during the CS epoch discriminated trial types whereas LH VGAT activity did not. *p = 0.017, ****p < 0.0001. (M) Maximal activity of individual LH VGAT neurons on CS + and CS − trials, without matching the sampled time bin. Dashed lines indicate sample CS + /CS − ratios. The LH VGAT centroid ratio was 1.26, indicating slight preference for CS + trials. (N) Similar to (M), but for LH LEPR neurons; the centroid ratio was 2.00, indicating large preference for CS + trials. (O) CS + selectivity index (CS + response/ΣCS responses) was higher for LH LEPR than LH VGAT neurons (p = 0.0034). Data represented as means ± SEMs. See also for full statistics.

    Journal: Cell reports

    Article Title: Lateral hypothalamic LEPR neurons drive appetitive but not consummatory behaviors

    doi: 10.1016/j.celrep.2021.109615

    Figure Lengend Snippet: (A) Schematic of deep brain calcium imaging. (B) Representative images of GRIN lens placement and field of view from Slc32a1 Cre and Lepr Cre mice. Scale bars: top, 500 μm; bottom, 100 μm. (C) Slc32a1 Cre (n = 9) and Lepr Cre (n = 8) mice used for functional imaging experiments on average performed most post-CS licks following CS + trials. (D) Normalized Ca 2+ traces of individual LH VGAT neurons on CS + or CS − trials. Vertical dashed lines indicate the beginning of the CS and outcome epochs. Horizontal dashed lines indicate groupings of neurons according to the epoch of maximal activity. (E–G) Normalized traces of CS + (orange) and CS − (gray) trials of (E) pre-responsive, (F) cue-responsive, and (G) reward-responsive LH VGAT neurons. (H–K) Similar to (E)–(G), except for LH LEPR neurons. (L) LH LEPR activity during the CS epoch discriminated trial types whereas LH VGAT activity did not. *p = 0.017, ****p < 0.0001. (M) Maximal activity of individual LH VGAT neurons on CS + and CS − trials, without matching the sampled time bin. Dashed lines indicate sample CS + /CS − ratios. The LH VGAT centroid ratio was 1.26, indicating slight preference for CS + trials. (N) Similar to (M), but for LH LEPR neurons; the centroid ratio was 2.00, indicating large preference for CS + trials. (O) CS + selectivity index (CS + response/ΣCS responses) was higher for LH LEPR than LH VGAT neurons (p = 0.0034). Data represented as means ± SEMs. See also for full statistics.

    Article Snippet: A miniature microscope with an integrated LED was used to image GCaMP6f fluorescence in LH VGAT and LH LEPR neurons through an implanted GRIN lens (Basic Fluorescence Snap-In Microscopy System – Deep Brain; Doric Lenses, Inc.).

    Techniques: Imaging, Functional Assay, Activity Assay

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: Lateral hypothalamic LEPR neurons drive appetitive but not consummatory behaviors

    doi: 10.1016/j.celrep.2021.109615

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Basic Fluorescence Snap-In Microscopy System - Deep Brain , Doric Lenses, Inc. , N/A.

    Techniques: Virus, Plasmid Preparation, Recombinant, Software, Fluorescence, Microscopy, Imaging

    Journal: eLife

    Article Title: An excitatory lateral hypothalamic circuit orchestrating pain behaviors in mice

    doi: 10.7554/eLife.66446

    Figure Lengend Snippet:

    Article Snippet: Other , Basic Fluorescence Snap-In Microscopy System – Deep Brain , Doric Lenses Inc , , In vivo imaging system.

    Techniques: Recombinant, Plasmid Preparation, Adjuvant, Software, Imaging, Fluorescence, Microscopy, In Vivo Imaging