mouse anti pax6 apc Search Results


antibody against pax 6  (Developmental Studies Hybridoma Bank)
96
Developmental Studies Hybridoma Bank antibody against pax 6
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mouse anti pax6 apc  (Novus Biologicals)
93
Novus Biologicals mouse anti pax6 apc
Mouse Anti Pax6 Apc, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pax6 miltenyi biotec human igg1 apc  (Miltenyi Biotec)
95
Miltenyi Biotec pax6 miltenyi biotec human igg1 apc
Pax6 Miltenyi Biotec Human Igg1 Apc, supplied by Miltenyi Biotec, 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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anti histag apc  (R&D Systems)
96
R&D Systems anti histag apc
Anti Histag Apc, supplied by R&D Systems, 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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ab 2733892 differentiation markers anti pax 6 human igg1 apc  (Miltenyi Biotec)
97
Miltenyi Biotec ab 2733892 differentiation markers anti pax 6 human igg1 apc
Ab 2733892 Differentiation Markers Anti Pax 6 Human Igg1 Apc, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse monoclonal antibody  (Boster Bio)
90
Boster Bio mouse monoclonal antibody
Mouse Monoclonal Antibody, supplied by Boster Bio, 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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ab5405 pax6 anti human pax 6 mouse  (Proteintech)
96
Proteintech ab5405 pax6 anti human pax 6 mouse
Ab5405 Pax6 Anti Human Pax 6 Mouse, supplied by Proteintech, 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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anti pax6 antibody  (Miltenyi Biotec)
95
Miltenyi Biotec anti pax6 antibody
In Vitro Differentiation Potential of iPSCs Derived from RECs into the Three Germ Layers: Mesoderm, Endoderm, and Ectoderm After 7 days of trilineage differentiation, cells with changed phenotypes (indicated with arrows) were observed. Flow cytometry analysis confirmed the differentiation of iPSCs (passages 3–7) into all three germ layers by detection of mesodermal (CD31 and SMA), definitive-endodermal (AFP and CXCR4), and neuroectodermal <t>(PAX6</t> and TUBB3) cells. Compared to controls, differentiated cells showed significantly increased expression of mesodermal, endodermal, and ectodermal markers. Scale bars of phase contrast microscopic pictures represent 100 μm. Results are shown as mean + SD (n = 4). Statistical differences were determined using one-way ANOVA followed by Bonferroni’s multiple comparison test (****p < 0.0001).
Anti Pax6 Antibody, supplied by Miltenyi Biotec, 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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anti pax6 peptide qvpgsepdmsqywprlq  (Covance)
90
Covance anti pax6 peptide qvpgsepdmsqywprlq
In Vitro Differentiation Potential of iPSCs Derived from RECs into the Three Germ Layers: Mesoderm, Endoderm, and Ectoderm After 7 days of trilineage differentiation, cells with changed phenotypes (indicated with arrows) were observed. Flow cytometry analysis confirmed the differentiation of iPSCs (passages 3–7) into all three germ layers by detection of mesodermal (CD31 and SMA), definitive-endodermal (AFP and CXCR4), and neuroectodermal <t>(PAX6</t> and TUBB3) cells. Compared to controls, differentiated cells showed significantly increased expression of mesodermal, endodermal, and ectodermal markers. Scale bars of phase contrast microscopic pictures represent 100 μm. Results are shown as mean + SD (n = 4). Statistical differences were determined using one-way ANOVA followed by Bonferroni’s multiple comparison test (****p < 0.0001).
Anti Pax6 Peptide Qvpgsepdmsqywprlq, supplied by Covance, 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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anti human pax6 antibody  (Miltenyi Biotec)
95
Miltenyi Biotec anti human pax6 antibody
In Vitro Differentiation Potential of iPSCs Derived from RECs into the Three Germ Layers: Mesoderm, Endoderm, and Ectoderm After 7 days of trilineage differentiation, cells with changed phenotypes (indicated with arrows) were observed. Flow cytometry analysis confirmed the differentiation of iPSCs (passages 3–7) into all three germ layers by detection of mesodermal (CD31 and SMA), definitive-endodermal (AFP and CXCR4), and neuroectodermal <t>(PAX6</t> and TUBB3) cells. Compared to controls, differentiated cells showed significantly increased expression of mesodermal, endodermal, and ectodermal markers. Scale bars of phase contrast microscopic pictures represent 100 μm. Results are shown as mean + SD (n = 4). Statistical differences were determined using one-way ANOVA followed by Bonferroni’s multiple comparison test (****p < 0.0001).
Anti Human Pax6 Antibody, supplied by Miltenyi Biotec, 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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anti pax 6  (Bethyl)
85
Bethyl anti pax 6
In Vitro Differentiation Potential of iPSCs Derived from RECs into the Three Germ Layers: Mesoderm, Endoderm, and Ectoderm After 7 days of trilineage differentiation, cells with changed phenotypes (indicated with arrows) were observed. Flow cytometry analysis confirmed the differentiation of iPSCs (passages 3–7) into all three germ layers by detection of mesodermal (CD31 and SMA), definitive-endodermal (AFP and CXCR4), and neuroectodermal <t>(PAX6</t> and TUBB3) cells. Compared to controls, differentiated cells showed significantly increased expression of mesodermal, endodermal, and ectodermal markers. Scale bars of phase contrast microscopic pictures represent 100 μm. Results are shown as mean + SD (n = 4). Statistical differences were determined using one-way ANOVA followed by Bonferroni’s multiple comparison test (****p < 0.0001).
Anti Pax 6, supplied by Bethyl, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pax6  (Boster Bio)
90
Boster Bio pax6
In Vitro Differentiation Potential of iPSCs Derived from RECs into the Three Germ Layers: Mesoderm, Endoderm, and Ectoderm After 7 days of trilineage differentiation, cells with changed phenotypes (indicated with arrows) were observed. Flow cytometry analysis confirmed the differentiation of iPSCs (passages 3–7) into all three germ layers by detection of mesodermal (CD31 and SMA), definitive-endodermal (AFP and CXCR4), and neuroectodermal <t>(PAX6</t> and TUBB3) cells. Compared to controls, differentiated cells showed significantly increased expression of mesodermal, endodermal, and ectodermal markers. Scale bars of phase contrast microscopic pictures represent 100 μm. Results are shown as mean + SD (n = 4). Statistical differences were determined using one-way ANOVA followed by Bonferroni’s multiple comparison test (****p < 0.0001).
Pax6, supplied by Boster Bio, 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


In Vitro Differentiation Potential of iPSCs Derived from RECs into the Three Germ Layers: Mesoderm, Endoderm, and Ectoderm After 7 days of trilineage differentiation, cells with changed phenotypes (indicated with arrows) were observed. Flow cytometry analysis confirmed the differentiation of iPSCs (passages 3–7) into all three germ layers by detection of mesodermal (CD31 and SMA), definitive-endodermal (AFP and CXCR4), and neuroectodermal (PAX6 and TUBB3) cells. Compared to controls, differentiated cells showed significantly increased expression of mesodermal, endodermal, and ectodermal markers. Scale bars of phase contrast microscopic pictures represent 100 μm. Results are shown as mean + SD (n = 4). Statistical differences were determined using one-way ANOVA followed by Bonferroni’s multiple comparison test (****p < 0.0001).

Journal: Molecular Therapy. Nucleic Acids

Article Title: Reprogramming of Urine-Derived Renal Epithelial Cells into iPSCs Using srRNA and Consecutive Differentiation into Beating Cardiomyocytes

doi: 10.1016/j.omtn.2019.07.016

Figure Lengend Snippet: In Vitro Differentiation Potential of iPSCs Derived from RECs into the Three Germ Layers: Mesoderm, Endoderm, and Ectoderm After 7 days of trilineage differentiation, cells with changed phenotypes (indicated with arrows) were observed. Flow cytometry analysis confirmed the differentiation of iPSCs (passages 3–7) into all three germ layers by detection of mesodermal (CD31 and SMA), definitive-endodermal (AFP and CXCR4), and neuroectodermal (PAX6 and TUBB3) cells. Compared to controls, differentiated cells showed significantly increased expression of mesodermal, endodermal, and ectodermal markers. Scale bars of phase contrast microscopic pictures represent 100 μm. Results are shown as mean + SD (n = 4). Statistical differences were determined using one-way ANOVA followed by Bonferroni’s multiple comparison test (****p < 0.0001).

Article Snippet: Ectodermal differentiation potential was assessed through the presence of neuroectoderm cells using PE-labeled anti-PAX6 antibody (Miltenyi Biotec) and Alexa Fluor 488-labeled anti-human neuron-specific TUBB3 antibody (BD Biosciences).

Techniques: In Vitro, Derivative Assay, Flow Cytometry, Expressing, Comparison