cat wa01 experimental models Search Results


99
WiCell Research Institute Inc h1 cell line
H1 Cell Line, supplied by WiCell Research Institute Inc, 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/product/cat+wa01+experimental+models/pm42031729-587-18-22?v=WiCell+Research+Institute+Inc
Average 99 stars, based on 1 article reviews
h1 cell line - by Bioz Stars, 2026-08
99/100 stars
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94
WiCell Research Institute Inc h1 primed hesc
H1 Primed Hesc, supplied by WiCell Research Institute Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cat+wa01+experimental+models/pmc11087464-434-8-11?v=WiCell+Research+Institute+Inc
Average 94 stars, based on 1 article reviews
h1 primed hesc - by Bioz Stars, 2026-08
94/100 stars
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99
ATCC wa01 hek293t cells atcc
Wa01 Hek293t Cells Atcc, 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
https://www.bioz.com/product/cat+wa01+experimental+models/pm37543038-190-49-52?v=ATCC
Average 99 stars, based on 1 article reviews
wa01 hek293t cells atcc - by Bioz Stars, 2026-08
99/100 stars
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90
WiCell Research Institute Inc embryonic stem cell hescs line h1
The process of reprogramming of Turner syndrome PBMCs into hiPSCs and characterization of hiPSCs-TS and colonies. ( A ) Schematic protocol used to reprogramming PBMCs into hiPSCs. ( B ) PBMCs with ten days of expansion in a specific medium for enrichment erythroblastic populations; the emergence of the first hiPSCs-TS colonies maintained in <t>hESCs</t> medium on MEF. ( C ) Characterization of hiPSCs-TS of Pt.1, Pt.2, Pt.3, Pt.4 and Pt.5. Phase contrast image showed hiPSCs maintained in mTeSR-1 medium on Geltrex; positively stain of alkaline phosphatase; Immunofluorescence assay showed the presence of pluripotency markers OCT4, SOX2, NANOG. Nuclei were stained with Hoechst (blue). Scale bars s: 200 μm and 100 μm. The data was compiled from at least three technical replicates. ( D ) Quantification of the relative expression of OCT4 , SOX2 , NANOG , KLF4 , and c-MYC genes in all hiPSCs lines and subclones (p15). Individual quantifications by qRT-PCR were normalized using the Β-ACTIN gene. The <t>ESCs-H1</t> line was used as a positive control and was not considered in the statistical model. All qRT-PCR from hiPSCs-TS and control data were compiled from at least three biological and technical replicates. p values were calculated by Two-way ANOVA, followed by Tukey’s multiple comparisons test as appropriate (letters a-b-c show difference between groups). Erros bars denote represent SD.
Embryonic Stem Cell Hescs Line H1, supplied by WiCell Research Institute 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/product/cat+wa01+experimental+models/pmc08624672-68-2-14?v=WiCell+Research+Institute+Inc
Average 90 stars, based on 1 article reviews
embryonic stem cell hescs line h1 - by Bioz Stars, 2026-08
90/100 stars
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90
Lonza normal human lung fibroblasts
The process of reprogramming of Turner syndrome PBMCs into hiPSCs and characterization of hiPSCs-TS and colonies. ( A ) Schematic protocol used to reprogramming PBMCs into hiPSCs. ( B ) PBMCs with ten days of expansion in a specific medium for enrichment erythroblastic populations; the emergence of the first hiPSCs-TS colonies maintained in <t>hESCs</t> medium on MEF. ( C ) Characterization of hiPSCs-TS of Pt.1, Pt.2, Pt.3, Pt.4 and Pt.5. Phase contrast image showed hiPSCs maintained in mTeSR-1 medium on Geltrex; positively stain of alkaline phosphatase; Immunofluorescence assay showed the presence of pluripotency markers OCT4, SOX2, NANOG. Nuclei were stained with Hoechst (blue). Scale bars s: 200 μm and 100 μm. The data was compiled from at least three technical replicates. ( D ) Quantification of the relative expression of OCT4 , SOX2 , NANOG , KLF4 , and c-MYC genes in all hiPSCs lines and subclones (p15). Individual quantifications by qRT-PCR were normalized using the Β-ACTIN gene. The <t>ESCs-H1</t> line was used as a positive control and was not considered in the statistical model. All qRT-PCR from hiPSCs-TS and control data were compiled from at least three biological and technical replicates. p values were calculated by Two-way ANOVA, followed by Tukey’s multiple comparisons test as appropriate (letters a-b-c show difference between groups). Erros bars denote represent SD.
Normal Human Lung Fibroblasts, 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/product/cat+wa01+experimental+models/pm40412386-257-110-114?v=Lonza
Average 90 stars, based on 1 article reviews
normal human lung fibroblasts - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

Image Search Results


The process of reprogramming of Turner syndrome PBMCs into hiPSCs and characterization of hiPSCs-TS and colonies. ( A ) Schematic protocol used to reprogramming PBMCs into hiPSCs. ( B ) PBMCs with ten days of expansion in a specific medium for enrichment erythroblastic populations; the emergence of the first hiPSCs-TS colonies maintained in hESCs medium on MEF. ( C ) Characterization of hiPSCs-TS of Pt.1, Pt.2, Pt.3, Pt.4 and Pt.5. Phase contrast image showed hiPSCs maintained in mTeSR-1 medium on Geltrex; positively stain of alkaline phosphatase; Immunofluorescence assay showed the presence of pluripotency markers OCT4, SOX2, NANOG. Nuclei were stained with Hoechst (blue). Scale bars s: 200 μm and 100 μm. The data was compiled from at least three technical replicates. ( D ) Quantification of the relative expression of OCT4 , SOX2 , NANOG , KLF4 , and c-MYC genes in all hiPSCs lines and subclones (p15). Individual quantifications by qRT-PCR were normalized using the Β-ACTIN gene. The ESCs-H1 line was used as a positive control and was not considered in the statistical model. All qRT-PCR from hiPSCs-TS and control data were compiled from at least three biological and technical replicates. p values were calculated by Two-way ANOVA, followed by Tukey’s multiple comparisons test as appropriate (letters a-b-c show difference between groups). Erros bars denote represent SD.

Journal: Cells

Article Title: Generation of Primordial Germ Cell-like Cells from iPSCs Derived from Turner Syndrome Patients

doi: 10.3390/cells10113099

Figure Lengend Snippet: The process of reprogramming of Turner syndrome PBMCs into hiPSCs and characterization of hiPSCs-TS and colonies. ( A ) Schematic protocol used to reprogramming PBMCs into hiPSCs. ( B ) PBMCs with ten days of expansion in a specific medium for enrichment erythroblastic populations; the emergence of the first hiPSCs-TS colonies maintained in hESCs medium on MEF. ( C ) Characterization of hiPSCs-TS of Pt.1, Pt.2, Pt.3, Pt.4 and Pt.5. Phase contrast image showed hiPSCs maintained in mTeSR-1 medium on Geltrex; positively stain of alkaline phosphatase; Immunofluorescence assay showed the presence of pluripotency markers OCT4, SOX2, NANOG. Nuclei were stained with Hoechst (blue). Scale bars s: 200 μm and 100 μm. The data was compiled from at least three technical replicates. ( D ) Quantification of the relative expression of OCT4 , SOX2 , NANOG , KLF4 , and c-MYC genes in all hiPSCs lines and subclones (p15). Individual quantifications by qRT-PCR were normalized using the Β-ACTIN gene. The ESCs-H1 line was used as a positive control and was not considered in the statistical model. All qRT-PCR from hiPSCs-TS and control data were compiled from at least three biological and technical replicates. p values were calculated by Two-way ANOVA, followed by Tukey’s multiple comparisons test as appropriate (letters a-b-c show difference between groups). Erros bars denote represent SD.

Article Snippet: The human embryonic stem cell (hESCs) line H1 (cat.# WA01-cGMP Material) was bought from WiCell International Stem Cell Bank, and was first published by Thomson et al. [ ].

Techniques: Staining, Immunofluorescence, Expressing, Quantitative RT-PCR, Positive Control

Cytogenetic analysis of all lines of hiPSCs-TS and controls. ( A – C ) phase contrast and karyotype of hESCs-H1 (p30) and hiPSCs male and female control (p20). 2). ( D – G ) phase contrast and karyotype of hiPSCs TS (p20). 3). ( H ) Phase contrast and karyotype of hiPSCs TS–Pt.2 (p20). Cytogenetic analyses revealed reciprocal chromosome translocations between chromosomes 11 with breakage at the q arm, and chromosome 12 with a breakpoint at the p arm (der(11;12)(q10;10), der(11;12)(p10;p10)). Scale bars indicate 400 μm.

Journal: Cells

Article Title: Generation of Primordial Germ Cell-like Cells from iPSCs Derived from Turner Syndrome Patients

doi: 10.3390/cells10113099

Figure Lengend Snippet: Cytogenetic analysis of all lines of hiPSCs-TS and controls. ( A – C ) phase contrast and karyotype of hESCs-H1 (p30) and hiPSCs male and female control (p20). 2). ( D – G ) phase contrast and karyotype of hiPSCs TS (p20). 3). ( H ) Phase contrast and karyotype of hiPSCs TS–Pt.2 (p20). Cytogenetic analyses revealed reciprocal chromosome translocations between chromosomes 11 with breakage at the q arm, and chromosome 12 with a breakpoint at the p arm (der(11;12)(q10;10), der(11;12)(p10;p10)). Scale bars indicate 400 μm.

Article Snippet: The human embryonic stem cell (hESCs) line H1 (cat.# WA01-cGMP Material) was bought from WiCell International Stem Cell Bank, and was first published by Thomson et al. [ ].

Techniques: