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nih3t3  (ATCC)


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    ATCC nih3t3
    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated <t>NIH3T3.</t> Bar represents 10 μm.
    Nih3t3, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 2387 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nih3t3+mouse+embryonic+fibroblasts/NIH%2F3T3%3B+Embryonic+Fibroblast%3B+Mouse/pmc12799909-18-0-2
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    Images

    1) Product Images from "Protocol to identify mechanosensitive nuclear proteins using tunable actomyosin contractility and proximity biotinylation in mammalian cells"

    Article Title: Protocol to identify mechanosensitive nuclear proteins using tunable actomyosin contractility and proximity biotinylation in mammalian cells

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2025.104288

    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated NIH3T3. Bar represents 10 μm.
    Figure Legend Snippet: Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated NIH3T3. Bar represents 10 μm.

    Techniques Used: Western Blot, Positive Control, Expressing, Immunofluorescence, Microscopy

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    Article Snippet: Bladder J82 and lung A549 cancer cell lines were purchased from the American Type Culture Collection (ATCC) (Rockville, MD, USA). .. NIH3T3 mouse embryonic fibroblasts were purchased from ATCC, and GGCT was overexpressed using the pCX4bsr retroviral vector as previously described . .. PC3, J82, and NIH3T3 cells were cultured in Dulbecco’s modified Eagle’s medium (#043-30085, Wako Pure Chemical Industries, Osaka, Japan), A498 cells in Eagle’s minimum essential medium (#055-08975, Wako), and A549 cells in RPMI-1640 (#05918, Nissui, Tokyo, Japan) supplemented with 300 μg/mL L -glutamine and 1 mmol/L sodium pyruvate.

    Article Title: Identification of c-Met as a novel target of γ-glutamylcyclotransferase.
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    Enzyme-linked Immunosorbent Assay:

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    cDNA Synthesis:

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    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated <t>NIH3T3.</t> Bar represents 10 μm.
    Nih3t3, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nih3t3+mouse+embryonic+fibroblasts/NIH%2F3T3%3B+Embryonic+Fibroblast%3B+Mouse/pmc12799909-18-0-2
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    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated <t>NIH3T3.</t> Bar represents 10 μm.
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    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated <t>NIH3T3.</t> Bar represents 10 μm.
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    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated <t>NIH3T3.</t> Bar represents 10 μm.
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    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated <t>NIH3T3.</t> Bar represents 10 μm.
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    SIS3 reprograms CAFs (a) Schematic representation depicting the in vitro activation of <t>NIH3T3</t> cells into CAFs using an OS-conditioned medium. (b) Western blotting is used to assess the expression levels of CAFs activation markers α-SMA and FAP. (c) Immunofluorescence (IF) staining is used to visualize the expression of CAFs activation markers α-SMA and FAP (scale bar: 25 μm). (d) IF staining is used to detect the expression of α-SMA and FAP in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 25 μm). (e) Statistical analysis of relative fluorescence intensity (FI), presented as mean ± SD (n = 3). (f) Schematic illustration of the TGF-β/SMAD3 signaling pathway. (g) Western blotting is used to evaluate the activation status of the TGF-β/SMAD3 signaling pathway in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative SMAD and p-SMAD expression, presented as mean ± SD (n = 3). (h) Representative images from collagen gel contraction assays on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative contraction degree, presented as mean ± SD (n = 3). (i) Representative images from wound healing assays conducted on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 200 μm) and the statistical analysis of relative wound healing degree, presented as mean ± SD (n = 3). (j) Representative images from transwell migration assays performed on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 100 μm) and the statistical analysis of the relative number of migrated cells, presented as mean ± SD (n = 3).
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    SIS3 reprograms CAFs (a) Schematic representation depicting the in vitro activation of <t>NIH3T3</t> cells into CAFs using an OS-conditioned medium. (b) Western blotting is used to assess the expression levels of CAFs activation markers α-SMA and FAP. (c) Immunofluorescence (IF) staining is used to visualize the expression of CAFs activation markers α-SMA and FAP (scale bar: 25 μm). (d) IF staining is used to detect the expression of α-SMA and FAP in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 25 μm). (e) Statistical analysis of relative fluorescence intensity (FI), presented as mean ± SD (n = 3). (f) Schematic illustration of the TGF-β/SMAD3 signaling pathway. (g) Western blotting is used to evaluate the activation status of the TGF-β/SMAD3 signaling pathway in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative SMAD and p-SMAD expression, presented as mean ± SD (n = 3). (h) Representative images from collagen gel contraction assays on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative contraction degree, presented as mean ± SD (n = 3). (i) Representative images from wound healing assays conducted on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 200 μm) and the statistical analysis of relative wound healing degree, presented as mean ± SD (n = 3). (j) Representative images from transwell migration assays performed on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 100 μm) and the statistical analysis of the relative number of migrated cells, presented as mean ± SD (n = 3).
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    Image Search Results


    Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated NIH3T3. Bar represents 10 μm.

    Journal: STAR Protocols

    Article Title: Protocol to identify mechanosensitive nuclear proteins using tunable actomyosin contractility and proximity biotinylation in mammalian cells

    doi: 10.1016/j.xpro.2025.104288

    Figure Lengend Snippet: Mechanosensitive responses of PTBP1 under various mechanical conditions (A) Volcano plot demonstrating significant nuclear enrichment of PTBP1 following tetracycline treatment (FDR< 0.01). Reprinted data with permission from Tseng et al. (B) Western blot analysis of PTBP1 nuclear enrichment, with YAP as a positive control. (C) Diagram shows the mechanical conditions used in this protocol to verify PTBP1 expression. Immunofluorescence microscopy confirming the nuclear accumulation of PTBP1 induced by high mechanical tension including low cell density (D, scale bar: 20 μm), stiff substrate (E, scale bar: 10 μm), and mechanical stretching (F, scale bar: 50 μm). (G) Immunofluorescence images showing PTBP1 nuclear reduction in ML-7 treated NIH3T3. Bar represents 10 μm.

    Article Snippet: NIH3T3 , ATCC , #CRL-1658; RRID: CVCL_0594.

    Techniques: Western Blot, Positive Control, Expressing, Immunofluorescence, Microscopy

    SIS3 reprograms CAFs (a) Schematic representation depicting the in vitro activation of NIH3T3 cells into CAFs using an OS-conditioned medium. (b) Western blotting is used to assess the expression levels of CAFs activation markers α-SMA and FAP. (c) Immunofluorescence (IF) staining is used to visualize the expression of CAFs activation markers α-SMA and FAP (scale bar: 25 μm). (d) IF staining is used to detect the expression of α-SMA and FAP in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 25 μm). (e) Statistical analysis of relative fluorescence intensity (FI), presented as mean ± SD (n = 3). (f) Schematic illustration of the TGF-β/SMAD3 signaling pathway. (g) Western blotting is used to evaluate the activation status of the TGF-β/SMAD3 signaling pathway in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative SMAD and p-SMAD expression, presented as mean ± SD (n = 3). (h) Representative images from collagen gel contraction assays on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative contraction degree, presented as mean ± SD (n = 3). (i) Representative images from wound healing assays conducted on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 200 μm) and the statistical analysis of relative wound healing degree, presented as mean ± SD (n = 3). (j) Representative images from transwell migration assays performed on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 100 μm) and the statistical analysis of the relative number of migrated cells, presented as mean ± SD (n = 3).

    Journal: Bioactive Materials

    Article Title: Hydrogel delivering antifibrotic agent and nano-sonosensitizer enhances efficacy of sonodynamic therapy in osteosarcoma treatment

    doi: 10.1016/j.bioactmat.2025.10.001

    Figure Lengend Snippet: SIS3 reprograms CAFs (a) Schematic representation depicting the in vitro activation of NIH3T3 cells into CAFs using an OS-conditioned medium. (b) Western blotting is used to assess the expression levels of CAFs activation markers α-SMA and FAP. (c) Immunofluorescence (IF) staining is used to visualize the expression of CAFs activation markers α-SMA and FAP (scale bar: 25 μm). (d) IF staining is used to detect the expression of α-SMA and FAP in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 25 μm). (e) Statistical analysis of relative fluorescence intensity (FI), presented as mean ± SD (n = 3). (f) Schematic illustration of the TGF-β/SMAD3 signaling pathway. (g) Western blotting is used to evaluate the activation status of the TGF-β/SMAD3 signaling pathway in NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative SMAD and p-SMAD expression, presented as mean ± SD (n = 3). (h) Representative images from collagen gel contraction assays on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 and the statistical analysis of relative contraction degree, presented as mean ± SD (n = 3). (i) Representative images from wound healing assays conducted on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 200 μm) and the statistical analysis of relative wound healing degree, presented as mean ± SD (n = 3). (j) Representative images from transwell migration assays performed on NIH3T3 cells, CAFs, and CAFs co-cultured with SIS3 (scale bar: 100 μm) and the statistical analysis of the relative number of migrated cells, presented as mean ± SD (n = 3).

    Article Snippet: The human OS cell line 143B, the mouse OS cell line K7M2, the mouse embryonic fibroblasts NIH3T3, and the human umbilical vein endothelial cells HUVEC were obtained from the American Type Culture Collection (ATCC, USA).

    Techniques: In Vitro, Activation Assay, Western Blot, Expressing, Immunofluorescence, Staining, Cell Culture, Fluorescence, Migration