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psox2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc psox2
    Psox2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 92/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/psox2/product/Cell Signaling Technology Inc
    Average 92 stars, based on 3 article reviews
    psox2 - by Bioz Stars, 2026-05
    92/100 stars

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    Fig. 1. Isolation of neural progenitor cells and immature neurons from the optic tectum. (A) Visual experience paradigm used to enrich for NPCs and immature neurons. Animals were reared in 12 h light/12 h dark until stage 46 when the midbrain was electroporated with <t>pSOX2-bd::tGFP</t> plasmid. After electroporation, animals were randomly divided into two groups, one exposed to enhanced visual experience (VE) for 24 h. (B) Whole brain electroporation labels NPCs and neurons in the optic tectum. Left: Image of the head of the tadpole with electrodes (yellow) on each side of the optic tectum. Middle: Dorsal view of the optic tectum. The ventricle, NPC layer, and neuronal layer are labeled. Right: in vivo 2-photon image of tGFP-labeled NPCs and neurons in the ventricular layer (VL) and neuronal layer (NL). (C) Fluorescence histogram indicates the gate setting of the fluorescence-activated cell sorting (FACS) to isolate tGFP+ cells. Control is set to the background fluorescence from nonelectroporated midbrain cells.
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    Fig. 1. Isolation of neural progenitor cells and immature neurons from the optic tectum. (A) Visual experience paradigm used to enrich for NPCs and immature neurons. Animals were reared in 12 h light/12 h dark until stage 46 when the midbrain was electroporated with <t>pSOX2-bd::tGFP</t> plasmid. After electroporation, animals were randomly divided into two groups, one exposed to enhanced visual experience (VE) for 24 h. (B) Whole brain electroporation labels NPCs and neurons in the optic tectum. Left: Image of the head of the tadpole with electrodes (yellow) on each side of the optic tectum. Middle: Dorsal view of the optic tectum. The ventricle, NPC layer, and neuronal layer are labeled. Right: in vivo 2-photon image of tGFP-labeled NPCs and neurons in the ventricular layer (VL) and neuronal layer (NL). (C) Fluorescence histogram indicates the gate setting of the fluorescence-activated cell sorting (FACS) to isolate tGFP+ cells. Control is set to the background fluorescence from nonelectroporated midbrain cells.
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    Fig. 1. Isolation of neural progenitor cells and immature neurons from the optic tectum. (A) Visual experience paradigm used to enrich for NPCs and immature neurons. Animals were reared in 12 h light/12 h dark until stage 46 when the midbrain was electroporated with pSOX2-bd::tGFP plasmid. After electroporation, animals were randomly divided into two groups, one exposed to enhanced visual experience (VE) for 24 h. (B) Whole brain electroporation labels NPCs and neurons in the optic tectum. Left: Image of the head of the tadpole with electrodes (yellow) on each side of the optic tectum. Middle: Dorsal view of the optic tectum. The ventricle, NPC layer, and neuronal layer are labeled. Right: in vivo 2-photon image of tGFP-labeled NPCs and neurons in the ventricular layer (VL) and neuronal layer (NL). (C) Fluorescence histogram indicates the gate setting of the fluorescence-activated cell sorting (FACS) to isolate tGFP+ cells. Control is set to the background fluorescence from nonelectroporated midbrain cells.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: BRCA1 and ELK-1 regulate neural progenitor cell fate in the optic tectum in response to visual experience in Xenopus laevis tadpoles.

    doi: 10.1073/pnas.2316542121

    Figure Lengend Snippet: Fig. 1. Isolation of neural progenitor cells and immature neurons from the optic tectum. (A) Visual experience paradigm used to enrich for NPCs and immature neurons. Animals were reared in 12 h light/12 h dark until stage 46 when the midbrain was electroporated with pSOX2-bd::tGFP plasmid. After electroporation, animals were randomly divided into two groups, one exposed to enhanced visual experience (VE) for 24 h. (B) Whole brain electroporation labels NPCs and neurons in the optic tectum. Left: Image of the head of the tadpole with electrodes (yellow) on each side of the optic tectum. Middle: Dorsal view of the optic tectum. The ventricle, NPC layer, and neuronal layer are labeled. Right: in vivo 2-photon image of tGFP-labeled NPCs and neurons in the ventricular layer (VL) and neuronal layer (NL). (C) Fluorescence histogram indicates the gate setting of the fluorescence-activated cell sorting (FACS) to isolate tGFP+ cells. Control is set to the background fluorescence from nonelectroporated midbrain cells.

    Article Snippet: All raw X. laevis data are available on GEO as GSE184315 (48) and on Xenbase. pSox2- bd::FP plasmid is available from Addgene, plasmid #34703.

    Techniques: Isolation, Plasmid Preparation, Electroporation, Labeling, In Vivo, Fluorescence, FACS, Control