minimum essential medium alpha media cat. Search Results


99
ATCC emem low glucose
Emem Low Glucose, 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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Corning Life Sciences minimum essential medium alpha
Minimum Essential Medium Alpha, 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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HiMedia Laboratories minimum essential medium-alpha
Minimum Essential Medium Alpha, supplied by HiMedia Laboratories, 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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Lonza emem medium
Emem Medium, 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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96
GE Healthcare minimum essential medium α
Minimum Essential Medium α, supplied by GE Healthcare, 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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90
HiMedia Laboratories high-glucose dulbecco's minimum essential medium dmem-hg al007a
High Glucose Dulbecco's Minimum Essential Medium Dmem Hg Al007a, supplied by HiMedia Laboratories, 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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96
GE Healthcare ɑ mem
Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by <t>culturing</t> <t>UCB</t> MSCs in myogenic differentiation <t>medium</t> M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.
ɑ Mem, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/ɑ mem/product/GE Healthcare
Average 96 stars, based on 1 article reviews
ɑ mem - by Bioz Stars, 2026-05
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90
Lonza eagle’s minimum essential medium (emem
Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by <t>culturing</t> <t>UCB</t> MSCs in myogenic differentiation <t>medium</t> M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.
Eagle’s Minimum Essential Medium (Emem, 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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Lonza minimum 9 essential medium-alpha αmem
Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by <t>culturing</t> <t>UCB</t> MSCs in myogenic differentiation <t>medium</t> M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.
Minimum 9 Essential Medium Alpha αmem, 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/minimum 9 essential medium-alpha αmem/product/Lonza
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90
Corning Life Sciences mem (minimum essential medium) alpha medium
Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by <t>culturing</t> <t>UCB</t> MSCs in myogenic differentiation <t>medium</t> M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.
Mem (Minimum Essential Medium) Alpha Medium, 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/mem (minimum essential medium) alpha medium/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
mem (minimum essential medium) alpha medium - by Bioz Stars, 2026-05
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90
Lonza minimum essential medium, alpha eagle be12-169f
Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by <t>culturing</t> <t>UCB</t> MSCs in myogenic differentiation <t>medium</t> M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.
Minimum Essential Medium, Alpha Eagle Be12 169f, 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/minimum essential medium, alpha eagle be12-169f/product/Lonza
Average 90 stars, based on 1 article reviews
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Lonza minimum essential medium alpha eagle
Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by <t>culturing</t> <t>UCB</t> MSCs in myogenic differentiation <t>medium</t> M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.
Minimum Essential Medium Alpha Eagle, 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/minimum essential medium alpha eagle/product/Lonza
Average 90 stars, based on 1 article reviews
minimum essential medium alpha eagle - by Bioz Stars, 2026-05
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Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by culturing UCB MSCs in myogenic differentiation medium M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.

Journal: Scientific Reports

Article Title: Umbilical cord tissue is a robust source for mesenchymal stem cells with enhanced myogenic differentiation potential compared to cord blood

doi: 10.1038/s41598-020-75102-9

Figure Lengend Snippet: Conversion of uMSCs into myogenic lineage. ( A ) Myogenic differentiation was induced by culturing UCB MSCs in myogenic differentiation medium M1 for 3, 6, and 10 days to detect Pax7, MyoD, Myogenin, and MyHC by ( i ) FACS and by ( ii ) immunocytochemistry. Nuclei were counterstained with DAPI. ( iii ) Myf5 mRNA expression in control and differentiated UCB MSCs after 3 days (* p = 0.03). ( iv ) Comparative immunofluorescent analysis of Pax7 and MyoD at 3 days, Myogenin at 7 days and MyHC at 10 days between UCT and UCB MSCs. UCT MSCs show increased expression of MyoD, Myogenin, and MyHC expressing cells compared to UCB MSCs at their corresponding time points (* p = 0.03). ( B ) Myogenin and MyHC mRNA expression in control UCT MSCs or UCT MSCs induced to differentiate in M1 medium with enhanced adhesion or M2 medium for 10 and 20 days (** p = 0.002). Robust expression of MyHC was observed in M1 medium with enhanced adhesion at 10 and 20 days.

Article Snippet: Further propagation of UCB and UCT derived MSCs was attained by plating in ɑ-MEM (Hyclone, cat # SH30568.FS) with 2 mM sodium pyruvate, 4 mM L-glutamine, 20% FBS, and antibiotics (henceforth referred to as growth medium), with the exception that UCB-derived MSCs were plated in growth medium supplemented with 1 ml of MesenPro growth supplement (ThermoFisher Scientific, cat # 12746012).

Techniques: Immunocytochemistry, Expressing