growth media f 12 Search Results


99
ATCC growth media
Growth Media, 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
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Thermo Fisher human interleukin 2
Human Interleukin 2, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Gemini Bio mpc growth media
Mpc Growth Media, supplied by Gemini Bio, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC dmem f12 media
Dmem F12 Media, 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
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ATCC dmem f12 growth medium
Dmem F12 Growth Medium, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/growth+media+f+12/Fetal+Bovine+Serum/us12383600-887-15-18
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ATCC growth media atcc medium
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Beijing Solarbio Science hfsc medium
Hfsc Medium, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems recombinant mouse interleukin 5
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Thermo Fisher growth media f 12
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Qiagen egm 2 growth media
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ATCC growth media f 12
Growth Media F 12, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/growth+media+f+12/PC-12/pmc04929735-55-19-23
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ZenBio preadipocyte growth medium
Adipogenesis following DOSS exposure in vitro . 3T3-L1 cells were grown to confluence over 72 hr in PGM <t>(preadipocyte</t> growth media). RFU, relative fluorescence units (firefly relative to renilla). Cells were either maintained in PGM or treated with MIM (minimal induction media) alone or supplemented with 10, 20, 25, or 50 ppm DOSS or 1 μM Rosi for an additional 3 days before analysis. ( A ) AdipoRed quantification of lipid accumulation as described in “Materials and Methods.” Data are expressed as mean ± SD; n = 5 per group (* p < 0.05 vs. MIM control). ( B ) Representative images of lipid accumulation of cells treated as in A (scale bar = 50 μm).
Preadipocyte Growth Medium, supplied by ZenBio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/growth+media+f+12/DMEM%2FF-12+Ham%E2%80%99s+(50%2F50)+with+glutamine+and+15mM+HEPES/pmc04710608-111-26-11
Average 93 stars, based on 1 article reviews
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Image Search Results


Adipogenesis following DOSS exposure in vitro . 3T3-L1 cells were grown to confluence over 72 hr in PGM (preadipocyte growth media). RFU, relative fluorescence units (firefly relative to renilla). Cells were either maintained in PGM or treated with MIM (minimal induction media) alone or supplemented with 10, 20, 25, or 50 ppm DOSS or 1 μM Rosi for an additional 3 days before analysis. ( A ) AdipoRed quantification of lipid accumulation as described in “Materials and Methods.” Data are expressed as mean ± SD; n = 5 per group (* p < 0.05 vs. MIM control). ( B ) Representative images of lipid accumulation of cells treated as in A (scale bar = 50 μm).

Journal: Environmental Health Perspectives

Article Title: Effects of Crude Oil/Dispersant Mixture and Dispersant Components on PPAR γ Activity in Vitro and in Vivo : Identification of Dioctyl Sodium Sulfosuccinate (DOSS; CAS #577-11-7) as a Probable Obesogen

doi: 10.1289/ehp.1409672

Figure Lengend Snippet: Adipogenesis following DOSS exposure in vitro . 3T3-L1 cells were grown to confluence over 72 hr in PGM (preadipocyte growth media). RFU, relative fluorescence units (firefly relative to renilla). Cells were either maintained in PGM or treated with MIM (minimal induction media) alone or supplemented with 10, 20, 25, or 50 ppm DOSS or 1 μM Rosi for an additional 3 days before analysis. ( A ) AdipoRed quantification of lipid accumulation as described in “Materials and Methods.” Data are expressed as mean ± SD; n = 5 per group (* p < 0.05 vs. MIM control). ( B ) Representative images of lipid accumulation of cells treated as in A (scale bar = 50 μm).

Article Snippet: For triacylglycerol staining assays to quantify adipogenic differentiation, 3T3-L1 preadipocyte cells (Zenbio) were plated in 48-well plates at a density of 10,000 cells per well in preadipocyte growth medium (PGM; DMEM/F12 supplemented as described above) and grown until confluence.

Techniques: In Vitro, Fluorescence