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calb1 chicken  (Neuromics)


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    Neuromics calb1 chicken
    ( A ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the cell proliferation marker Ki67. ( B ) Quantitation of the number of Ki67-positive cells in the external granular layer of WT and Dp10 animals. Graph shows mean ± SD. N=3. Mann-Whitney U test. ( C ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the Purkinje cell marker calbindin <t>(CALB1)</t> and the microtubule binding protein doublecortin (DCX). The far-right panel shows insets of DCX staining. ( D ) Quantitation of primary cilia frequency in the inner granule layer of WT and Dp10 animals normalized to WT. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( E ) Representative tiled confocal images of the cerebellum from P21 wild-type (WT) and Dp10 animals. Brain sections were stained with Hoechst 33342, ARL13B, and γ-tubulin. Insets show zoomed in regions corresponding to the same folia in each animal. ( F ) Quantitation of primary cilia frequency in WT and Dp animals at P21 normalized to WT at P21. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( G–H ) Quantitation of the granular layer ( G ) and molecular layer ( H ) widths in WT and Dp10 animals at P21. Graphs show mean ± SD. N=3. Mann-Whitney U test.
    Calb1 Chicken, supplied by Neuromics, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/calb1 chicken/product/Neuromics
    Average 94 stars, based on 2 article reviews
    calb1 chicken - by Bioz Stars, 2026-04
    94/100 stars

    Images

    1) Product Images from "Trisomy 21 induces pericentrosomal crowding delaying primary ciliogenesis and mouse cerebellar development"

    Article Title: Trisomy 21 induces pericentrosomal crowding delaying primary ciliogenesis and mouse cerebellar development

    Journal: eLife

    doi: 10.7554/eLife.78202

    ( A ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the cell proliferation marker Ki67. ( B ) Quantitation of the number of Ki67-positive cells in the external granular layer of WT and Dp10 animals. Graph shows mean ± SD. N=3. Mann-Whitney U test. ( C ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the Purkinje cell marker calbindin (CALB1) and the microtubule binding protein doublecortin (DCX). The far-right panel shows insets of DCX staining. ( D ) Quantitation of primary cilia frequency in the inner granule layer of WT and Dp10 animals normalized to WT. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( E ) Representative tiled confocal images of the cerebellum from P21 wild-type (WT) and Dp10 animals. Brain sections were stained with Hoechst 33342, ARL13B, and γ-tubulin. Insets show zoomed in regions corresponding to the same folia in each animal. ( F ) Quantitation of primary cilia frequency in WT and Dp animals at P21 normalized to WT at P21. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( G–H ) Quantitation of the granular layer ( G ) and molecular layer ( H ) widths in WT and Dp10 animals at P21. Graphs show mean ± SD. N=3. Mann-Whitney U test.
    Figure Legend Snippet: ( A ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the cell proliferation marker Ki67. ( B ) Quantitation of the number of Ki67-positive cells in the external granular layer of WT and Dp10 animals. Graph shows mean ± SD. N=3. Mann-Whitney U test. ( C ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the Purkinje cell marker calbindin (CALB1) and the microtubule binding protein doublecortin (DCX). The far-right panel shows insets of DCX staining. ( D ) Quantitation of primary cilia frequency in the inner granule layer of WT and Dp10 animals normalized to WT. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( E ) Representative tiled confocal images of the cerebellum from P21 wild-type (WT) and Dp10 animals. Brain sections were stained with Hoechst 33342, ARL13B, and γ-tubulin. Insets show zoomed in regions corresponding to the same folia in each animal. ( F ) Quantitation of primary cilia frequency in WT and Dp animals at P21 normalized to WT at P21. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( G–H ) Quantitation of the granular layer ( G ) and molecular layer ( H ) widths in WT and Dp10 animals at P21. Graphs show mean ± SD. N=3. Mann-Whitney U test.

    Techniques Used: Staining, Marker, Quantitation Assay, MANN-WHITNEY, Binding Assay


    Figure Legend Snippet:

    Techniques Used: Transduction, Marker, Transfection, Construct, Plasmid Preparation, Sequencing, Negative Control, Antibody Labeling



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    ( A ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the cell proliferation marker Ki67. ( B ) Quantitation of the number of Ki67-positive cells in the external granular layer of WT and Dp10 animals. Graph shows mean ± SD. N=3. Mann-Whitney U test. ( C ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the Purkinje cell marker calbindin <t>(CALB1)</t> and the microtubule binding protein doublecortin (DCX). The far-right panel shows insets of DCX staining. ( D ) Quantitation of primary cilia frequency in the inner granule layer of WT and Dp10 animals normalized to WT. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( E ) Representative tiled confocal images of the cerebellum from P21 wild-type (WT) and Dp10 animals. Brain sections were stained with Hoechst 33342, ARL13B, and γ-tubulin. Insets show zoomed in regions corresponding to the same folia in each animal. ( F ) Quantitation of primary cilia frequency in WT and Dp animals at P21 normalized to WT at P21. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( G–H ) Quantitation of the granular layer ( G ) and molecular layer ( H ) widths in WT and Dp10 animals at P21. Graphs show mean ± SD. N=3. Mann-Whitney U test.
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    Image Search Results


    ( A ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the cell proliferation marker Ki67. ( B ) Quantitation of the number of Ki67-positive cells in the external granular layer of WT and Dp10 animals. Graph shows mean ± SD. N=3. Mann-Whitney U test. ( C ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the Purkinje cell marker calbindin (CALB1) and the microtubule binding protein doublecortin (DCX). The far-right panel shows insets of DCX staining. ( D ) Quantitation of primary cilia frequency in the inner granule layer of WT and Dp10 animals normalized to WT. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( E ) Representative tiled confocal images of the cerebellum from P21 wild-type (WT) and Dp10 animals. Brain sections were stained with Hoechst 33342, ARL13B, and γ-tubulin. Insets show zoomed in regions corresponding to the same folia in each animal. ( F ) Quantitation of primary cilia frequency in WT and Dp animals at P21 normalized to WT at P21. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( G–H ) Quantitation of the granular layer ( G ) and molecular layer ( H ) widths in WT and Dp10 animals at P21. Graphs show mean ± SD. N=3. Mann-Whitney U test.

    Journal: eLife

    Article Title: Trisomy 21 induces pericentrosomal crowding delaying primary ciliogenesis and mouse cerebellar development

    doi: 10.7554/eLife.78202

    Figure Lengend Snippet: ( A ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the cell proliferation marker Ki67. ( B ) Quantitation of the number of Ki67-positive cells in the external granular layer of WT and Dp10 animals. Graph shows mean ± SD. N=3. Mann-Whitney U test. ( C ) Representative tiled confocal images of WT and Dp10 P4 animals corresponding to the same cerebellar folia in each animal. Brain sections were stained with Hoechst 33342 and the Purkinje cell marker calbindin (CALB1) and the microtubule binding protein doublecortin (DCX). The far-right panel shows insets of DCX staining. ( D ) Quantitation of primary cilia frequency in the inner granule layer of WT and Dp10 animals normalized to WT. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( E ) Representative tiled confocal images of the cerebellum from P21 wild-type (WT) and Dp10 animals. Brain sections were stained with Hoechst 33342, ARL13B, and γ-tubulin. Insets show zoomed in regions corresponding to the same folia in each animal. ( F ) Quantitation of primary cilia frequency in WT and Dp animals at P21 normalized to WT at P21. Graph shows mean ± SD. N=3. Wilcoxon matched-pairs test. ( G–H ) Quantitation of the granular layer ( G ) and molecular layer ( H ) widths in WT and Dp10 animals at P21. Graphs show mean ± SD. N=3. Mann-Whitney U test.

    Article Snippet: Antibody , CALB1 (chicken) , Neuromics , Cat# CH22118, RRID: AB_2737107 , IF (1:1000).

    Techniques: Staining, Marker, Quantitation Assay, MANN-WHITNEY, Binding Assay

    Journal: eLife

    Article Title: Trisomy 21 induces pericentrosomal crowding delaying primary ciliogenesis and mouse cerebellar development

    doi: 10.7554/eLife.78202

    Figure Lengend Snippet:

    Article Snippet: Antibody , CALB1 (chicken) , Neuromics , Cat# CH22118, RRID: AB_2737107 , IF (1:1000).

    Techniques: Transduction, Marker, Transfection, Construct, Plasmid Preparation, Sequencing, Negative Control, Antibody Labeling

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    Article Title: Molecular characteristics and laminar distribution of prefrontal neurons projecting to the mesolimbic system

    doi: 10.7554/eLife.78813

    Figure Lengend Snippet:

    Article Snippet: Antibody , Anti-Calb1 (chicken polyclonal) , Synaptic Systems , 214 006, RRID: AB_261990 , 1:2000.

    Techniques: Plasmid Preparation, Recombinant, Molecular Weight, Software, Immunohistochemistry, Staining

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    Journal: The Journal of comparative neurology

    Article Title: Pou3f4-Expressing Otic Mesenchyme Cells Promote Spiral Ganglion Neuron Survival in the Postnatal Mouse Cochlea

    doi: 10.1002/cne.24867

    Figure Lengend Snippet: Primary antibodies used.

    Article Snippet: Calb1 ( Figure 7a – i ) , Raised against full length recombinant human Calbindin , On a western blot, anti-Calb1 recognizes a 30kD band from rat brain lysate and tagged recombinant calbindin; anti-Calb1 does not recognize tagged recombinant parvalbumin or calretinin (manufacturers technical data). , Abeomics, chicken polyclonal, Cat# 34–1020, RRID: AB_2810884 , 1:500.

    Techniques: Concentration Assay, Purification, Immunostaining, Western Blot, Labeling, Immunocytochemistry, Fluorescence, Cell Culture, Staining, Blocking Assay, Produced, Recombinant, Gene Expression, Variant Assay, Expressing, Transfection, Control, Over Expression, Plasmid Preparation