cell culture media dmem Search Results


cell culture plates 1.2% agar in dmem  (Corning Life Sciences)
90
Corning Life Sciences cell culture plates 1.2% agar in dmem
Cell Culture Plates 1.2% Agar In Dmem, 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 plates 1.2% agar in dmem - by Bioz Stars, 2026-03
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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 for adhesion cell cultures  (PanEco Scientific)
90
PanEco Scientific dmem for adhesion cell cultures
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 For Adhesion Cell Cultures, supplied by PanEco Scientific, 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 for adhesion cell cultures - 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
https://www.bioz.com/result/dmem cell culture medium/product/Keygen Biotech
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dmem cell culture medium - by Bioz Stars, 2026-03
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dmem cell culture media  (Genetix Biotech)
90
Genetix Biotech dmem cell culture 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).
Dmem Cell Culture Media, supplied by Genetix Biotech, 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 media/product/Genetix Biotech
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dmem cell culture media - by Bioz Stars, 2026-03
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cell culture reagents dmem  (Nissui Pharmaceutical)
90
Nissui Pharmaceutical cell culture reagents dmem
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 Reagents Dmem, supplied by Nissui Pharmaceutical, 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 reagents dmem/product/Nissui Pharmaceutical
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cell culture reagents dmem - by Bioz Stars, 2026-03
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es cell culture broth es-dmem  (VITROMEX Inc)
90
VITROMEX Inc es cell culture broth es-dmem
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).
Es Cell Culture Broth Es Dmem, supplied by VITROMEX Inc, 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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es cell culture broth es-dmem - by Bioz Stars, 2026-03
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basal cell culture liquid media—dmem and ham's f-12  (Corning Life Sciences)
90
Corning Life Sciences basal cell culture liquid media—dmem and ham's f-12
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).
Basal Cell Culture Liquid Media—Dmem And Ham's F 12, 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
https://www.bioz.com/result/basal cell culture liquid media—dmem and ham's f-12/product/Corning Life Sciences
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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