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msc adipogenic differentiation medium  (ScienCell)

 
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    ScienCell msc adipogenic differentiation medium
    Comparison of MPC and <t>MSC</t> morphology, surface markers, and their differentiation ability. (A) Morphological characteristics of MSCs and MPCs under microscopy (10×; scale bar: 200 µm). (B) Alizarin Red staining for osteogenic differentiation and Oil Red O staining or <t>adipogenic</t> differentiation (4×; scale bar: 500 µm; **P<0.01). (C) Flow cytometry showing the expression of positive surface markers of MPCs and MSCs (n=3): CD90, CD105, and CD73. (D) Flow cytometry showing the expression of negative surface markers for MPCs and MSCs (n=3): CD45, CD14, CD34, CD11b, and CD31. MSC, mesenchymal stem cell; MPC, mesenchymal progenitor cell.
    Msc Adipogenic Differentiation Medium, supplied by ScienCell, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/msc+adipogenic+differentiation+medium/msc+adipogenic+differentiation+medium/pmc11002474-109-14-20
    Average 90 stars, based on 1 article reviews
    msc adipogenic differentiation medium - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Tumor-derived mesenchymal progenitor cell-related genes in the regulation of breast cancer proliferation"

    Article Title: Tumor-derived mesenchymal progenitor cell-related genes in the regulation of breast cancer proliferation

    Journal: Gland Surgery

    doi: 10.21037/gs-23-387

    Comparison of MPC and MSC morphology, surface markers, and their differentiation ability. (A) Morphological characteristics of MSCs and MPCs under microscopy (10×; scale bar: 200 µm). (B) Alizarin Red staining for osteogenic differentiation and Oil Red O staining or adipogenic differentiation (4×; scale bar: 500 µm; **P<0.01). (C) Flow cytometry showing the expression of positive surface markers of MPCs and MSCs (n=3): CD90, CD105, and CD73. (D) Flow cytometry showing the expression of negative surface markers for MPCs and MSCs (n=3): CD45, CD14, CD34, CD11b, and CD31. MSC, mesenchymal stem cell; MPC, mesenchymal progenitor cell.
    Figure Legend Snippet: Comparison of MPC and MSC morphology, surface markers, and their differentiation ability. (A) Morphological characteristics of MSCs and MPCs under microscopy (10×; scale bar: 200 µm). (B) Alizarin Red staining for osteogenic differentiation and Oil Red O staining or adipogenic differentiation (4×; scale bar: 500 µm; **P<0.01). (C) Flow cytometry showing the expression of positive surface markers of MPCs and MSCs (n=3): CD90, CD105, and CD73. (D) Flow cytometry showing the expression of negative surface markers for MPCs and MSCs (n=3): CD45, CD14, CD34, CD11b, and CD31. MSC, mesenchymal stem cell; MPC, mesenchymal progenitor cell.

    Techniques Used: Comparison, Microscopy, Staining, Flow Cytometry, Expressing

    Related Articles

    Cell Differentiation:

    Article Title: Transcriptome analysis of tumor-derived mesenchymal progenitor cells shows that CHST15 is a fibrosis regulator of retroperitoneal liposarcoma
    Article Snippet: The proliferation indices were analyzed using Modfit LT TM 5 (Verity Software House, Topsham, ME, USA). .. Cell differentiation assays Upon reaching 100% confluence, the MSC complete medium was replaced with MSC adipogenic or osteogenic differentiation medium (ScienCell, Carlsbad, CA, USA) for 18–21 or 14–16 days, respectively, according to the manufacturer’s instructions. .. After differentiation, the cells were stained with Oil Red O (Solarbio, Beijing, China) for adipogenic differentiation and Alizarin Red S (Solarbio) for osteogenic differentiation, respectively, according to the manufacturer’s instructions.

    Cell Culture:

    Article Title: Tumor-derived mesenchymal progenitor cell-related genes in the regulation of breast cancer proliferation
    Article Snippet: We adjusted the data for compensation and analyzed the data using FlowJo software (BD Biosciences). .. After MSCs and MPCs reached 100% confluence, the MSC completion medium was replaced with MSC adipogenic or osteogenic differentiation medium (ScienCell Research Laboratories) and cultured for 20 or 15 days. .. Adipogenic differentiation and osteogenic differentiation were determined via staining with Oil Red O and Alizarin Red S (Solarbio, China), respectively.



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    Image Search Results


    Comparison of MPC and MSC morphology, surface markers, and their differentiation ability. (A) Morphological characteristics of MSCs and MPCs under microscopy (10×; scale bar: 200 µm). (B) Alizarin Red staining for osteogenic differentiation and Oil Red O staining or adipogenic differentiation (4×; scale bar: 500 µm; **P<0.01). (C) Flow cytometry showing the expression of positive surface markers of MPCs and MSCs (n=3): CD90, CD105, and CD73. (D) Flow cytometry showing the expression of negative surface markers for MPCs and MSCs (n=3): CD45, CD14, CD34, CD11b, and CD31. MSC, mesenchymal stem cell; MPC, mesenchymal progenitor cell.

    Journal: Gland Surgery

    Article Title: Tumor-derived mesenchymal progenitor cell-related genes in the regulation of breast cancer proliferation

    doi: 10.21037/gs-23-387

    Figure Lengend Snippet: Comparison of MPC and MSC morphology, surface markers, and their differentiation ability. (A) Morphological characteristics of MSCs and MPCs under microscopy (10×; scale bar: 200 µm). (B) Alizarin Red staining for osteogenic differentiation and Oil Red O staining or adipogenic differentiation (4×; scale bar: 500 µm; **P<0.01). (C) Flow cytometry showing the expression of positive surface markers of MPCs and MSCs (n=3): CD90, CD105, and CD73. (D) Flow cytometry showing the expression of negative surface markers for MPCs and MSCs (n=3): CD45, CD14, CD34, CD11b, and CD31. MSC, mesenchymal stem cell; MPC, mesenchymal progenitor cell.

    Article Snippet: After MSCs and MPCs reached 100% confluence, the MSC completion medium was replaced with MSC adipogenic or osteogenic differentiation medium (ScienCell Research Laboratories) and cultured for 20 or 15 days.

    Techniques: Comparison, Microscopy, Staining, Flow Cytometry, Expressing