Review



adipogenic differentiation medium  (Thermo Fisher)


Bioz Verified Symbol Thermo Fisher is a verified supplier
Bioz Manufacturer Symbol Thermo Fisher manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    Thermo Fisher adipogenic differentiation medium
    Adipogenic Differentiation Medium, supplied by Thermo Fisher, 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/result/adipogenic differentiation medium/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    adipogenic differentiation medium - by Bioz Stars, 2026-03
    90/100 stars

    Images



    Similar Products

    mesenchymal stem cell adipogenic differentiation medium 2  (PromoCell)
    95
    PromoCell mesenchymal stem cell adipogenic differentiation medium 2
    Mesenchymal Stem Cell Adipogenic Differentiation Medium 2, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mesenchymal stem cell adipogenic differentiation medium 2/product/PromoCell
    Average 95 stars, based on 1 article reviews
    mesenchymal stem cell adipogenic differentiation medium 2 - by Bioz Stars, 2026-03
    95/100 stars
    		  Buy from Supplier
    msc adipogenic differentiation medium 2  (PromoCell)
    95
    PromoCell msc adipogenic differentiation medium 2
    Msc Adipogenic Differentiation Medium 2, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/msc adipogenic differentiation medium 2/product/PromoCell
    Average 95 stars, based on 1 article reviews
    msc adipogenic differentiation medium 2 - by Bioz Stars, 2026-03
    95/100 stars
    		  Buy from Supplier
    oricell sd rat bone marrow mesenchymal stem cell adipogenic differentiation basal medium  (Cyagen Biosciences)
    90
    Cyagen Biosciences oricell sd rat bone marrow mesenchymal stem cell adipogenic differentiation basal medium
    Schematic conceptualization of this study. IR activated the NF-κB signaling pathway to promote activation and maturation of DCs, amplifying inflammatory signals through the release of pro-inflammatory cytokines. The mDCs triggered oxidative stress of BMSCs, showing increased intracellular ROS levels, inhibited osteogenic differentiation, and enhanced <t>adipogenic</t> differentiation, which accelerated the progression of radiation-induced jaw injury. VitD3-induced tolDCs exhibited IR resistance and anti-inflammatory properties, possessing the therapeutic potential to accelerate bone regeneration in irradiated jaw defects through local administration. (IR: ionizing radiation; mDC: mature dendritic cell; tolDC: tolerogenic dendritic cell; BMSC: bone marrow <t>mesenchymal</t> stem cell; ROS: reactive oxygen species; vitamin D3: vitD3)
    Oricell Sd Rat Bone Marrow Mesenchymal Stem Cell Adipogenic Differentiation Basal Medium, supplied by Cyagen Biosciences, 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/result/oricell sd rat bone marrow mesenchymal stem cell adipogenic differentiation basal medium/product/Cyagen Biosciences
    Average 90 stars, based on 1 article reviews
    oricell sd rat bone marrow mesenchymal stem cell adipogenic differentiation basal medium - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    adipogenic differentiation medium huxuc-01001  (Cyagen Biosciences)
    90
    Cyagen Biosciences adipogenic differentiation medium huxuc-01001
    Schematic conceptualization of this study. IR activated the NF-κB signaling pathway to promote activation and maturation of DCs, amplifying inflammatory signals through the release of pro-inflammatory cytokines. The mDCs triggered oxidative stress of BMSCs, showing increased intracellular ROS levels, inhibited osteogenic differentiation, and enhanced <t>adipogenic</t> differentiation, which accelerated the progression of radiation-induced jaw injury. VitD3-induced tolDCs exhibited IR resistance and anti-inflammatory properties, possessing the therapeutic potential to accelerate bone regeneration in irradiated jaw defects through local administration. (IR: ionizing radiation; mDC: mature dendritic cell; tolDC: tolerogenic dendritic cell; BMSC: bone marrow <t>mesenchymal</t> stem cell; ROS: reactive oxygen species; vitamin D3: vitD3)
    Adipogenic Differentiation Medium Huxuc 01001, supplied by Cyagen Biosciences, 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/result/adipogenic differentiation medium huxuc-01001/product/Cyagen Biosciences
    Average 90 stars, based on 1 article reviews
    adipogenic differentiation medium huxuc-01001 - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    adipogenic differentiation medium  (Cyagen Biosciences)
    90
    Cyagen Biosciences adipogenic differentiation medium
    Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of <t>adipogenic</t> induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”
    Adipogenic Differentiation Medium, supplied by Cyagen Biosciences, 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/result/adipogenic differentiation medium/product/Cyagen Biosciences
    Average 90 stars, based on 1 article reviews
    adipogenic differentiation medium - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    adipogenic induction medium (hmsc adipogenic differentiation bulletkit)  (Lonza)
    90
    Lonza adipogenic induction medium (hmsc adipogenic differentiation bulletkit)
    Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of <t>adipogenic</t> induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”
    Adipogenic Induction Medium (Hmsc Adipogenic Differentiation Bulletkit), supplied by Lonza, 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/result/adipogenic induction medium (hmsc adipogenic differentiation bulletkit)/product/Lonza
    Average 90 stars, based on 1 article reviews
    adipogenic induction medium (hmsc adipogenic differentiation bulletkit) - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    adipogenic differentiation medium a  (Cyagen Biosciences)
    90
    Cyagen Biosciences adipogenic differentiation medium a
    Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of <t>adipogenic</t> induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”
    Adipogenic Differentiation Medium A, supplied by Cyagen Biosciences, 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/result/adipogenic differentiation medium a/product/Cyagen Biosciences
    Average 90 stars, based on 1 article reviews
    adipogenic differentiation medium a - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    chondrogenic differentiation medium  (PromoCell)
    95
    PromoCell chondrogenic differentiation medium
    Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of <t>adipogenic</t> induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”
    Chondrogenic Differentiation Medium, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/chondrogenic differentiation medium/product/PromoCell
    Average 95 stars, based on 1 article reviews
    chondrogenic differentiation medium - by Bioz Stars, 2026-03
    95/100 stars
    		  Buy from Supplier
    adipogenic differentiation medium  (Thermo Fisher)
    90
    Thermo Fisher adipogenic differentiation medium
    Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of <t>adipogenic</t> induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”
    Adipogenic Differentiation Medium, supplied by Thermo Fisher, 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/result/adipogenic differentiation medium/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    adipogenic differentiation medium - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    adipogenic differentiation medium 2  (PromoCell)
    95
    PromoCell adipogenic differentiation medium 2
    Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of <t>adipogenic</t> induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”
    Adipogenic Differentiation Medium 2, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/adipogenic differentiation medium 2/product/PromoCell
    Average 95 stars, based on 1 article reviews
    adipogenic differentiation medium 2 - by Bioz Stars, 2026-03
    95/100 stars
    		  Buy from Supplier

    Image Search Results


    Schematic conceptualization of this study. IR activated the NF-κB signaling pathway to promote activation and maturation of DCs, amplifying inflammatory signals through the release of pro-inflammatory cytokines. The mDCs triggered oxidative stress of BMSCs, showing increased intracellular ROS levels, inhibited osteogenic differentiation, and enhanced adipogenic differentiation, which accelerated the progression of radiation-induced jaw injury. VitD3-induced tolDCs exhibited IR resistance and anti-inflammatory properties, possessing the therapeutic potential to accelerate bone regeneration in irradiated jaw defects through local administration. (IR: ionizing radiation; mDC: mature dendritic cell; tolDC: tolerogenic dendritic cell; BMSC: bone marrow mesenchymal stem cell; ROS: reactive oxygen species; vitamin D3: vitD3)

    Journal: Stem Cell Research & Therapy

    Article Title: Ionizing radiation-mediated dendritic cell maturation exacerbates inflammatory response of bone marrow mesenchymal stem cells and impairs osteogenesis in radiation-induced jaw injury

    doi: 10.1186/s13287-025-04508-x

    Figure Lengend Snippet: Schematic conceptualization of this study. IR activated the NF-κB signaling pathway to promote activation and maturation of DCs, amplifying inflammatory signals through the release of pro-inflammatory cytokines. The mDCs triggered oxidative stress of BMSCs, showing increased intracellular ROS levels, inhibited osteogenic differentiation, and enhanced adipogenic differentiation, which accelerated the progression of radiation-induced jaw injury. VitD3-induced tolDCs exhibited IR resistance and anti-inflammatory properties, possessing the therapeutic potential to accelerate bone regeneration in irradiated jaw defects through local administration. (IR: ionizing radiation; mDC: mature dendritic cell; tolDC: tolerogenic dendritic cell; BMSC: bone marrow mesenchymal stem cell; ROS: reactive oxygen species; vitamin D3: vitD3)

    Article Snippet: BMSCs were co-cultured with DC-CM and OriCell SD rat bone marrow mesenchymal stem cell adipogenic differentiation basal medium (Cyagen, USA) for 7 days.

    Techniques: Activation Assay, Irradiation

    Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of adipogenic induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”

    Journal: BMC Oral Health

    Article Title: Piezo1 participates in the tension-driven osteogenic differentiation of periodontal ligament stem cells

    doi: 10.1186/s12903-025-06427-y

    Figure Lengend Snippet: Characterization of hPDLSCs and changes in the cell cytoskeleton and viability after tension force application. ( A ) Morphology of the 3th generation hPDLSCs. Original magnification ×40. ( B ) After 3 weeks of osteogenic induction, hPDLSCs formed calcified nodules with a reddish coloration. Original magnification ×100. ( C ) After 2 weeks of adipogenic induction, hPDLSCs developed spherical lipid accumulations. Original magnification ×100. ( D ) The expression rates of positive markers (Strol-1, CD44, CD146, and CD90) were 98.2%, 99.2%, 99.8% and 99.6%, respectively, while the negative markers CD45 and CD34 showed positive expression rates of 0.51% and 0.94%, respectively. ( E ) The growth curve was represented as a “S shape.” ( F ) The cell viability in the 0, 1, 3, 6, 9, and 12 h groups showed no significant differences, as shown by CCK-8 assays. ( G ) Immunofluorescence staining of F-actin in hPDLSCs in the 0, 1, 3, 6, 9, 12 h groups. (red, F-actin; blue, DAPI). Scale bar = 10 μm. Data are presented as “mean ± standard deviation”

    Article Snippet: Upon reaching 80–100% confluency, hPDLSCs were cultured in a pre-prepared osteogenic or adipogenic differentiation medium (Cyagen Biosciences, CA, USA) for 1–4 weeks as per the manufacturer’s protocol.

    Techniques: Expressing, CCK-8 Assay, Immunofluorescence, Staining, Standard Deviation