esc growth medium Search Results


96
ATCC esc growth medium
Esc Growth Medium, supplied by ATCC, 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/esc growth medium/product/ATCC
Average 96 stars, based on 1 article reviews
esc growth medium - by Bioz Stars, 2026-02
96/100 stars
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99
Thermo Fisher esc growth medium
Esc Growth Medium, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/esc growth medium/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
esc growth medium - by Bioz Stars, 2026-02
99/100 stars
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90
StemRD Inc psgro-free human ipsc/esc growth medium
Psgro Free Human Ipsc/Esc Growth Medium, supplied by StemRD 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/psgro-free human ipsc/esc growth medium/product/StemRD Inc
Average 90 stars, based on 1 article reviews
psgro-free human ipsc/esc growth medium - by Bioz Stars, 2026-02
90/100 stars
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99
Thermo Fisher pluripotent stem cells
Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully <t>pluripotent</t> cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.
Pluripotent Stem Cells, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/pluripotent stem cells/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
pluripotent stem cells - by Bioz Stars, 2026-02
99/100 stars
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90
Millipore es1: esc growth medium
Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully <t>pluripotent</t> cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.
Es1: Esc Growth Medium, supplied by Millipore, 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/es1: esc growth medium/product/Millipore
Average 90 stars, based on 1 article reviews
es1: esc growth medium - by Bioz Stars, 2026-02
90/100 stars
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90
Thermo Fisher knockout dulbecco's modified eagle's medium (dmem)
Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully <t>pluripotent</t> cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.
Knockout Dulbecco's Modified Eagle's Medium (Dmem), 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/knockout dulbecco's modified eagle's medium (dmem)/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
knockout dulbecco's modified eagle's medium (dmem) - by Bioz Stars, 2026-02
90/100 stars
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99
InvivoGen esc growth medium
Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully <t>pluripotent</t> cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.
Esc Growth Medium, supplied by InvivoGen, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/esc growth medium/product/InvivoGen
Average 99 stars, based on 1 article reviews
esc growth medium - by Bioz Stars, 2026-02
99/100 stars
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90
Thermo Fisher esc growth medium (knockout-dmem
Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully <t>pluripotent</t> cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.
Esc Growth Medium (Knockout Dmem, 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/esc growth medium (knockout-dmem/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
esc growth medium (knockout-dmem - by Bioz Stars, 2026-02
90/100 stars
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90
STEMCELL Technologies Inc mtesr1
Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully <t>pluripotent</t> cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.
Mtesr1, supplied by STEMCELL Technologies 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/mtesr1/product/STEMCELL Technologies Inc
Average 90 stars, based on 1 article reviews
mtesr1 - by Bioz Stars, 2026-02
90/100 stars
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90
Cyagen Biosciences mouse esc growth medium
Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully <t>pluripotent</t> cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.
Mouse Esc Growth 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/mouse esc growth medium/product/Cyagen Biosciences
Average 90 stars, based on 1 article reviews
mouse esc growth medium - by Bioz Stars, 2026-02
90/100 stars
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Image Search Results


Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully pluripotent cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.

Journal: Cell Cycle

Article Title: Induced pluripotent stem cells derived from human amnion in chemically defined conditions

doi: 10.1080/15384101.2017.1403690

Figure Lengend Snippet: Morphology, characterization and reprogramming progression of the source AMSC. A. Cultured AMSC display a morphology of mesenchymal stem cells – elongated and spindle-shaped. B. Flow cytometric analysis of AMSC revealed expression of CD44, CD73, CD166, CD105, N-cadherin and CD90. Activation of the epithelial marker EpCAM was low. This expression profile is consistent with a mesenchymal stem cell phenotype. C. Morphological progression of reprogramming in AMSC transfected with 3 episomal reprogramming plasmids (3E). Days following transfection are denoted by “d” and the passage number following transfection by “p”. On day 6 (left), cells assuming cobblestone-like epithelial shape and undergoing MET were clearly discernible (ellipse). On day 17 (two middle pictures), partially and fully pluripotent cell colonies were both present, with partially pluripotent colonies being more abundant. Fully pluripotent colonies were expanded and clonal cultures established (right). Scale bar = 200 µm.

Article Snippet: AFSC amniotic fluid stem cells AM-iPSC / AM[N] induced pluripotent stem cells derived from amniotic membrane stem cells, N is line/patient number AMSC amniotic membrane stem cells bFGF basic fibroblast growth factor DAPI 4′,6-diamidino-2-phenylindole E8 chemically defined medium for culture of human pluripotent stem cells [ 27 ] EDTA ethylenediaminetetraacetic acid EGF epidermal growth factor ESC embryonic stem cells FASTQ raw sequencing file format, contains sequence and quality FBS fetal bovine serum IGF insulin-like growth factor iPSC induced pluripotent stem cells KSR KnockOutTM Serum Replacement (Thermo-Fisher Scientific) MEF mouse embryonic fibroblast feeder layer MET mesenchymal-to-epithelial transition MSC mesenchymal stem cells PBS phosphate buffered saline PSC pluripotent stem cells – embryonic and induced pluripotent stem cells VTN recombinant human vitronectin GRN gene regulatory networks FDR false discovery rate

Techniques: Cell Culture, Expressing, Activation Assay, Marker, Transfection

Flow cytometric analysis of the expression of ESC markers in AM-iPSC in their mature state grown in VTN-E8 conditions. Antibodies against markers Oct3/4A, Nanog, TRA-1-60 and SSEA-1 were conjugated to AlexaFluor 488 and Sox2, TRA-1-81 and SSEA-4 to AlexaFluor 647. All plots show the corresponding marker fluorescence on the horizontal axis on a log 10 scale and side scatter on a linear scale on the vertical axis. All 4 lines of AM-iPSC showed typical human primed pluripotent stem cell marker expression profile – Oct3/4A, Nanog, Sox2, TRA-1-60, TRA-1-81 and SSEA-4 being expressed in the majority of cells, while SSEA-1 is negative. The morphology of the corresponding lines is also shown, scale bar = 100µm.

Journal: Cell Cycle

Article Title: Induced pluripotent stem cells derived from human amnion in chemically defined conditions

doi: 10.1080/15384101.2017.1403690

Figure Lengend Snippet: Flow cytometric analysis of the expression of ESC markers in AM-iPSC in their mature state grown in VTN-E8 conditions. Antibodies against markers Oct3/4A, Nanog, TRA-1-60 and SSEA-1 were conjugated to AlexaFluor 488 and Sox2, TRA-1-81 and SSEA-4 to AlexaFluor 647. All plots show the corresponding marker fluorescence on the horizontal axis on a log 10 scale and side scatter on a linear scale on the vertical axis. All 4 lines of AM-iPSC showed typical human primed pluripotent stem cell marker expression profile – Oct3/4A, Nanog, Sox2, TRA-1-60, TRA-1-81 and SSEA-4 being expressed in the majority of cells, while SSEA-1 is negative. The morphology of the corresponding lines is also shown, scale bar = 100µm.

Article Snippet: AFSC amniotic fluid stem cells AM-iPSC / AM[N] induced pluripotent stem cells derived from amniotic membrane stem cells, N is line/patient number AMSC amniotic membrane stem cells bFGF basic fibroblast growth factor DAPI 4′,6-diamidino-2-phenylindole E8 chemically defined medium for culture of human pluripotent stem cells [ 27 ] EDTA ethylenediaminetetraacetic acid EGF epidermal growth factor ESC embryonic stem cells FASTQ raw sequencing file format, contains sequence and quality FBS fetal bovine serum IGF insulin-like growth factor iPSC induced pluripotent stem cells KSR KnockOutTM Serum Replacement (Thermo-Fisher Scientific) MEF mouse embryonic fibroblast feeder layer MET mesenchymal-to-epithelial transition MSC mesenchymal stem cells PBS phosphate buffered saline PSC pluripotent stem cells – embryonic and induced pluripotent stem cells VTN recombinant human vitronectin GRN gene regulatory networks FDR false discovery rate

Techniques: Expressing, Marker, Fluorescence

Analysis of the transcriptional profile of AM-iPSC by PluriTest. Control ESC line WA25 and iPSC line MIRJT7i (WiCell) were included. Also included were 3 iPSC lines grown in standard non-defined KSR-supplemented MEF-conditioned culture conditions (KSR-CM), two of which – AM3 and AM4 – were isogenic to AM3 and AM4 grown in defined VTN/E8 conditions. A. Hierarchical clustering of the lines showed AM5 having a distinct profile and KSR-CM lines being the most similar to the ESC line WA25. B. A plot of PluriTest classifiers “novelty” and “pluripotency”. The red cloud represents the cluster area of validated PSC lines (grown in standard KSR-CM culture condition). The blue cloud represents the cluster area of differentiated cells. The light blue cloud represents the cluster area of partially pluripotent stem cells. Each point represents a replicate of one line. All lines were identified as pluripotent but clustering outside of the red cloud. C. Pluripotency scores in individual lines, with AM5 scoring the highest and AM3 the lowest. D. Novelty scored in individual lines, with AM5 scoring the lowest and AM3 the highest. High pluripotency score and low novelty score render the transcriptional profile of AM5 the most similar to the typical pluripotent profile. ** p<0.01, *** p<0.001.

Journal: Cell Cycle

Article Title: Induced pluripotent stem cells derived from human amnion in chemically defined conditions

doi: 10.1080/15384101.2017.1403690

Figure Lengend Snippet: Analysis of the transcriptional profile of AM-iPSC by PluriTest. Control ESC line WA25 and iPSC line MIRJT7i (WiCell) were included. Also included were 3 iPSC lines grown in standard non-defined KSR-supplemented MEF-conditioned culture conditions (KSR-CM), two of which – AM3 and AM4 – were isogenic to AM3 and AM4 grown in defined VTN/E8 conditions. A. Hierarchical clustering of the lines showed AM5 having a distinct profile and KSR-CM lines being the most similar to the ESC line WA25. B. A plot of PluriTest classifiers “novelty” and “pluripotency”. The red cloud represents the cluster area of validated PSC lines (grown in standard KSR-CM culture condition). The blue cloud represents the cluster area of differentiated cells. The light blue cloud represents the cluster area of partially pluripotent stem cells. Each point represents a replicate of one line. All lines were identified as pluripotent but clustering outside of the red cloud. C. Pluripotency scores in individual lines, with AM5 scoring the highest and AM3 the lowest. D. Novelty scored in individual lines, with AM5 scoring the lowest and AM3 the highest. High pluripotency score and low novelty score render the transcriptional profile of AM5 the most similar to the typical pluripotent profile. ** p<0.01, *** p<0.001.

Article Snippet: AFSC amniotic fluid stem cells AM-iPSC / AM[N] induced pluripotent stem cells derived from amniotic membrane stem cells, N is line/patient number AMSC amniotic membrane stem cells bFGF basic fibroblast growth factor DAPI 4′,6-diamidino-2-phenylindole E8 chemically defined medium for culture of human pluripotent stem cells [ 27 ] EDTA ethylenediaminetetraacetic acid EGF epidermal growth factor ESC embryonic stem cells FASTQ raw sequencing file format, contains sequence and quality FBS fetal bovine serum IGF insulin-like growth factor iPSC induced pluripotent stem cells KSR KnockOutTM Serum Replacement (Thermo-Fisher Scientific) MEF mouse embryonic fibroblast feeder layer MET mesenchymal-to-epithelial transition MSC mesenchymal stem cells PBS phosphate buffered saline PSC pluripotent stem cells – embryonic and induced pluripotent stem cells VTN recombinant human vitronectin GRN gene regulatory networks FDR false discovery rate

Techniques: Control