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g1 s phase  (MedChemExpress)


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    Structured Review

    MedChemExpress g1 s phase
    G1 S Phase, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 96/100, based on 103 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/g1+s+phase/G-1/pmc13045141-45-5-13
    Average 96 stars, based on 103 article reviews
    g1 s phase - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    other:

    Article Title: USP1 driven mitotic dysregulation and PLK1 stabilization confer Lenvatinib resistance in hepatocellular carcinoma.
    Article Snippet: Cells were synchronized at the G1/S phase by treatment with 2 mM thymidine (MedChemExpress) for 24 hours, followed by release into fresh medium for 10 hours.

    Article Title: USP1 driven mitotic dysregulation and PLK1 stabilization confer Lenvatinib resistance in hepatocellular carcinoma
    Article Snippet: Cells were synchronized at the G1/S phase by treatment with 2 mM thymidine (MedChemExpress) for 24 h, followed by release into fresh medium for 10 h. Subsequently, cells were treated with 10 μM MG132 for 2.5 h to synchronize at metaphase.



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    Fig. 4. Subcutaneous adipose tissue promoted vascularization and cell proliferation in expanded skin by means of paracrine growth factors. (Above) Immunohistochemical staining for CD31 and <t>PCNA</t> to mark ves- sels and <t>proliferating</t> cells. (Center) mRNA expression levels of EGF, bFGF, and VEGF in skin samples from the control group and the AT group (AT-Skin), and adipose tissue from the AT group (AT-Adipose). (Below, right) Immunoblot analysis of the expression of bFGF, EGF, and VEGF in skin samples from the control group and the AT group, and adipose tissue from the AT group. Scale bar = 100 µm; *P < 0.05; ***P < 0.001.
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    Fig. 4. Subcutaneous adipose tissue promoted vascularization and cell proliferation in expanded skin by means of paracrine growth factors. (Above) Immunohistochemical staining for CD31 and PCNA to mark ves- sels and proliferating cells. (Center) mRNA expression levels of EGF, bFGF, and VEGF in skin samples from the control group and the AT group (AT-Skin), and adipose tissue from the AT group (AT-Adipose). (Below, right) Immunoblot analysis of the expression of bFGF, EGF, and VEGF in skin samples from the control group and the AT group, and adipose tissue from the AT group. Scale bar = 100 µm; *P < 0.05; ***P < 0.001.

    Journal: Plastic & Reconstructive Surgery

    Article Title: Tracing the Change and Contribution of Subcutaneous Adipose to Skin Expansion Using a Luciferase-Transgenic Fat Transplantation Model

    doi: 10.1097/prs.0000000000010753

    Figure Lengend Snippet: Fig. 4. Subcutaneous adipose tissue promoted vascularization and cell proliferation in expanded skin by means of paracrine growth factors. (Above) Immunohistochemical staining for CD31 and PCNA to mark ves- sels and proliferating cells. (Center) mRNA expression levels of EGF, bFGF, and VEGF in skin samples from the control group and the AT group (AT-Skin), and adipose tissue from the AT group (AT-Adipose). (Below, right) Immunoblot analysis of the expression of bFGF, EGF, and VEGF in skin samples from the control group and the AT group, and adipose tissue from the AT group. Scale bar = 100 µm; *P < 0.05; ***P < 0.001.

    Article Snippet: To detect the vessels and proliferating cells (early G1 and S phases) in expanded skin, rabbit anti-rat CD31 (BM2966; Boster, Wuhan, People’s Republic of China) and mouse anti-rat proliferating cell nuclear antigen (PCNA) (BM0104; Boster) antibodies were applied.

    Techniques: Immunohistochemical staining, Staining, Expressing, Control, Western Blot