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differentiation n2a cells  (ATCC)


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    ATCC differentiation n2a cells
    Differentiation N2a Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 4096 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/differentiation n2a cells/product/ATCC
    Average 99 stars, based on 4096 article reviews
    differentiation n2a cells - by Bioz Stars, 2026-05
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    Effect of Znf179 on neuronal differentiation. (A,B ) Knockdown of Znf179 expression diminished neuronal differentiation and dendritic arborization in primary cerebellar granule cells. Primary culture of cerebellar granule cells from cerebella of wild-type or Znf-179-knockout mice were stained with anti-MAP2 (red) and DAPI (white). The Quantification of the percentage of MAP2(+) cells is shown in the histogram. ** p = 0.0018. Scale bar, 50 μm. ( n > 300, groups were compared using t -test, two-tailed p value). (C,D) <t>N2a</t> cells with and without stable expression of GFP-Znf179 proteins were induced to differentiate in MEM containing 2% serum for 24 h. The overexpression of GFP-Znf179 induced N2a cell differentiation in both 10% and 2% serum-containing medium, while those in 2% serum-containing medium exhibited longer neurite lengths (the lower right panel in 1 C). Significant neurite branching was observed in differentiated N2a cells. Differentiated and total N2a cells were determined in at least five fields of views, and at least 600 cells were counted in total. Quantification of the percentage of differentiated N2a cells is shown in the histogram. *** p < 0.001. Scale bar, 50 μm. ( n > 600, groups were compared by a one-way ANOVA, two-tailed p value). (E) Total cell lysates of N2a cells were analyzed by Western blotting using anti-MAP2, anti-Znf179, anti-Tuj-1, anti-GFAP, anti-α-tubulin and anti-GAPDH antibodies. Uncropped images are in Supplementary Figure .
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    Effect of Znf179 on neuronal differentiation. (A,B ) Knockdown of Znf179 expression diminished neuronal differentiation and dendritic arborization in primary cerebellar granule cells. Primary culture of cerebellar granule cells from cerebella of wild-type or Znf-179-knockout mice were stained with anti-MAP2 (red) and DAPI (white). The Quantification of the percentage of MAP2(+) cells is shown in the histogram. ** p = 0.0018. Scale bar, 50 μm. ( n > 300, groups were compared using t -test, two-tailed p value). (C,D) <t>N2a</t> cells with and without stable expression of GFP-Znf179 proteins were induced to differentiate in MEM containing 2% serum for 24 h. The overexpression of GFP-Znf179 induced N2a cell differentiation in both 10% and 2% serum-containing medium, while those in 2% serum-containing medium exhibited longer neurite lengths (the lower right panel in 1 C). Significant neurite branching was observed in differentiated N2a cells. Differentiated and total N2a cells were determined in at least five fields of views, and at least 600 cells were counted in total. Quantification of the percentage of differentiated N2a cells is shown in the histogram. *** p < 0.001. Scale bar, 50 μm. ( n > 600, groups were compared by a one-way ANOVA, two-tailed p value). (E) Total cell lysates of N2a cells were analyzed by Western blotting using anti-MAP2, anti-Znf179, anti-Tuj-1, anti-GFAP, anti-α-tubulin and anti-GAPDH antibodies. Uncropped images are in Supplementary Figure .
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    Effect of Znf179 on neuronal differentiation. (A,B ) Knockdown of Znf179 expression diminished neuronal differentiation and dendritic arborization in primary cerebellar granule cells. Primary culture of cerebellar granule cells from cerebella of wild-type or Znf-179-knockout mice were stained with anti-MAP2 (red) and DAPI (white). The Quantification of the percentage of MAP2(+) cells is shown in the histogram. ** p = 0.0018. Scale bar, 50 μm. ( n > 300, groups were compared using t -test, two-tailed p value). (C,D) N2a cells with and without stable expression of GFP-Znf179 proteins were induced to differentiate in MEM containing 2% serum for 24 h. The overexpression of GFP-Znf179 induced N2a cell differentiation in both 10% and 2% serum-containing medium, while those in 2% serum-containing medium exhibited longer neurite lengths (the lower right panel in 1 C). Significant neurite branching was observed in differentiated N2a cells. Differentiated and total N2a cells were determined in at least five fields of views, and at least 600 cells were counted in total. Quantification of the percentage of differentiated N2a cells is shown in the histogram. *** p < 0.001. Scale bar, 50 μm. ( n > 600, groups were compared by a one-way ANOVA, two-tailed p value). (E) Total cell lysates of N2a cells were analyzed by Western blotting using anti-MAP2, anti-Znf179, anti-Tuj-1, anti-GFAP, anti-α-tubulin and anti-GAPDH antibodies. Uncropped images are in Supplementary Figure .

    Journal: Scientific Reports

    Article Title: Znf179 induces differentiation and growth arrest of human primary glioblastoma multiforme in a p53-dependent cell cycle pathway

    doi: 10.1038/s41598-017-05305-0

    Figure Lengend Snippet: Effect of Znf179 on neuronal differentiation. (A,B ) Knockdown of Znf179 expression diminished neuronal differentiation and dendritic arborization in primary cerebellar granule cells. Primary culture of cerebellar granule cells from cerebella of wild-type or Znf-179-knockout mice were stained with anti-MAP2 (red) and DAPI (white). The Quantification of the percentage of MAP2(+) cells is shown in the histogram. ** p = 0.0018. Scale bar, 50 μm. ( n > 300, groups were compared using t -test, two-tailed p value). (C,D) N2a cells with and without stable expression of GFP-Znf179 proteins were induced to differentiate in MEM containing 2% serum for 24 h. The overexpression of GFP-Znf179 induced N2a cell differentiation in both 10% and 2% serum-containing medium, while those in 2% serum-containing medium exhibited longer neurite lengths (the lower right panel in 1 C). Significant neurite branching was observed in differentiated N2a cells. Differentiated and total N2a cells were determined in at least five fields of views, and at least 600 cells were counted in total. Quantification of the percentage of differentiated N2a cells is shown in the histogram. *** p < 0.001. Scale bar, 50 μm. ( n > 600, groups were compared by a one-way ANOVA, two-tailed p value). (E) Total cell lysates of N2a cells were analyzed by Western blotting using anti-MAP2, anti-Znf179, anti-Tuj-1, anti-GFAP, anti-α-tubulin and anti-GAPDH antibodies. Uncropped images are in Supplementary Figure .

    Article Snippet: Total and differentiated N2a cells were determined in at least five FOVs, and at least 600 cells were counted in total by MetaMorph.

    Techniques: Knockdown, Expressing, Knock-Out, Staining, Two Tailed Test, Over Expression, Cell Differentiation, Western Blot