cell culture medium dmem Search Results


cell culture media dmems  (Lonza)
90
Lonza cell culture media dmems
Cell Culture Media Dmems, 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
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cell culture media dmems - by Bioz Stars, 2026-03
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cell culture medium dmem  (Cellgro)
90
Cellgro cell culture medium dmem
Cell Culture Medium Dmem, supplied by Cellgro, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cell culture medium dmem - by Bioz Stars, 2026-03
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culture media for the different cancer cell lines  (PAN - Biotech)
90
PAN - Biotech culture media for the different cancer cell lines
Culture Media For The Different Cancer Cell Lines, supplied by PAN - Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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culture media for the different cancer cell lines - by Bioz Stars, 2026-03
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dmem cell culture medium cellgro) sodium pyruvate  (Mediatech)
90
Mediatech dmem cell culture medium cellgro) sodium pyruvate
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Dmem Cell Culture Medium Cellgro) Sodium Pyruvate, supplied by Mediatech, 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/dmem cell culture medium cellgro) sodium pyruvate/product/Mediatech
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dmem cell culture medium cellgro) sodium pyruvate - by Bioz Stars, 2026-03
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cell culture medium [dmem: 70%; m3:basef (cat. no. m300f-500; incell llc)]: 20%; fbs: 10  (iCell Bioscience Inc)
90
iCell Bioscience Inc cell culture medium [dmem: 70%; m3:basef (cat. no. m300f-500; incell llc)]: 20%; fbs: 10
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Cell Culture Medium [Dmem: 70%; M3:Basef (Cat. No. M300f 500; Incell Llc)]: 20%; Fbs: 10, supplied by iCell Bioscience Inc, 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/cell culture medium [dmem: 70%; m3:basef (cat. no. m300f-500; incell llc)]: 20%; fbs: 10/product/iCell Bioscience Inc
Average 90 stars, based on 1 article reviews
cell culture medium [dmem: 70%; m3:basef (cat. no. m300f-500; incell llc)]: 20%; fbs: 10 - by Bioz Stars, 2026-03
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dmem cell culture medium  (Keygen Biotech)
90
Keygen Biotech dmem cell culture medium
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Dmem Cell Culture Medium, supplied by Keygen Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dmem cell culture medium - by Bioz Stars, 2026-03
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cell culture media dulbecco’s modified eagle’s medium (dmem), -glutamine, penicillin and streptomycin  (Biochrom)
90
Biochrom cell culture media dulbecco’s modified eagle’s medium (dmem), -glutamine, penicillin and streptomycin
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Cell Culture Media Dulbecco’s Modified Eagle’s Medium (Dmem), Glutamine, Penicillin And Streptomycin, supplied by Biochrom, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
cell culture media dulbecco’s modified eagle’s medium (dmem), -glutamine, penicillin and streptomycin - by Bioz Stars, 2026-03
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powdered dmem cell culture medium  (Merck & Co)
90
Merck & Co powdered dmem cell culture medium
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Powdered Dmem Cell Culture Medium, supplied by Merck & Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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powdered dmem cell culture medium - by Bioz Stars, 2026-03
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dmem cell culture medium  (Merck KGaA)
90
Merck KGaA dmem cell culture medium
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Dmem Cell Culture Medium, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dmem cell culture medium - by Bioz Stars, 2026-03
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cell culture medium dulbecco’s modified eagle’s medium (dmem) provided by  (MatTek)
90
MatTek cell culture medium dulbecco’s modified eagle’s medium (dmem) provided by
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Cell Culture Medium Dulbecco’s Modified Eagle’s Medium (Dmem) Provided By, supplied by MatTek, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cell culture medium dulbecco’s modified eagle’s medium (dmem) provided by - by Bioz Stars, 2026-03
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cell culture medium dmem corning 10-013-cv  (Corning Life Sciences)
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Corning Life Sciences cell culture medium dmem corning 10-013-cv
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Cell Culture Medium Dmem Corning 10 013 Cv, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cell culture medium dmem corning 10-013-cv - by Bioz Stars, 2026-03
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dulbecco’s modified eagle’s medium (dmem) media  (PRIMACYT Cell Culture Technology GmbH)
90
PRIMACYT Cell Culture Technology GmbH dulbecco’s modified eagle’s medium (dmem) media
Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in <t>DMEM</t> containing <t>10%</t> <t>dialyzed</t> serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).
Dulbecco’s Modified Eagle’s Medium (Dmem) Media, supplied by PRIMACYT Cell Culture Technology GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in DMEM containing 10% dialyzed serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).

Journal: Analytical chemistry

Article Title: Liquid chromatography - high resolution mass spectrometry analysis of fatty acid metabolism

doi: 10.1021/ac202220b

Figure Lengend Snippet: Peak intensities of (A) long-chain fatty acids (C14–C24) and (B) very-long-chain fatty acids (C26–C36) from immortalized baby mouse kidney epithelial cells with or without expression of activated Ras. The cells were grown to 80% confluence in 6 cm culture dishes in DMEM containing 10% dialyzed serum and unlabeled glucose and glutamine. The extracted and saponified fatty acids were resuspended in 1:1:0.3 chloroform/methanol/water solution to a final concentration of 2 μl packed cell volume per 1 ml solvent for analysis of the more abundant long-chain fatty acids, and to a 45-fold higher concentration (90 μl cell volume per 1 mL solvent) for analysis of the less abundant very-long-chain fatty acids, and samples analyzed by LC-MS. Resulting peak heights were corrected for residual differences in total fatty acids injected between the two cell lines by correcting individual peak intensities with the total ion current (TIC) for a given sample. Bars indicate mean ± SD (N=3). * indicate significant differences in FA levels between parental and activated Ras expressing cells (p < 0.05, unpaired two-tailed t-test equal variance, Bonferroni corrected).

Article Snippet: DMEM cell culture medium (Mediatech Cellgro) without sodium pyruvate, PBS (HyClone), and dialyzed fetal bovine serum (dFBS, HyClone) were acquired from Fisher Scientific (Pittsburgh, PA).

Techniques: Expressing, Concentration Assay, Liquid Chromatography with Mass Spectroscopy, Injection, Two Tailed Test

13C-labeling patterns for very-long-chain monounsaturated fatty acids from immortalized baby mouse kidney epithelial cells with and without expression of activated Ras. Cells were maintained for 72 hour in DMEM with U-13C-glucose and U-13C-glutamine and 10% dialyzed FBS. In the schematic drawing of the fatty acids, * represent 13C atoms. The double bonds are shown at their most likely position but have not been experimentally determined. Bars indicate mean ± standard deviation (N=2).

Journal: Analytical chemistry

Article Title: Liquid chromatography - high resolution mass spectrometry analysis of fatty acid metabolism

doi: 10.1021/ac202220b

Figure Lengend Snippet: 13C-labeling patterns for very-long-chain monounsaturated fatty acids from immortalized baby mouse kidney epithelial cells with and without expression of activated Ras. Cells were maintained for 72 hour in DMEM with U-13C-glucose and U-13C-glutamine and 10% dialyzed FBS. In the schematic drawing of the fatty acids, * represent 13C atoms. The double bonds are shown at their most likely position but have not been experimentally determined. Bars indicate mean ± standard deviation (N=2).

Article Snippet: DMEM cell culture medium (Mediatech Cellgro) without sodium pyruvate, PBS (HyClone), and dialyzed fetal bovine serum (dFBS, HyClone) were acquired from Fisher Scientific (Pittsburgh, PA).

Techniques: Labeling, Expressing, Standard Deviation