human os cell lines saos 2 htb 85 Search Results


98
ATCC cells saos 2
Cells Saos 2, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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hos  (ATCC)
98
ATCC hos
Hos, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+os+cell+lines+saos+2+htb+85/MG-63/pm12740912-38-6-19
Average 98 stars, based on 1 article reviews
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96
ATCC human osteosarcoma cell line
Human Osteosarcoma Cell Line, 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/product/human+os+cell+lines+saos+2+htb+85/Saos-2%3B+Osteosarcoma%3B+Human/10__1074_slash_jbc__m109932200-52-14-19
Average 96 stars, based on 1 article reviews
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u2os  (ATCC)
98
ATCC u2os
SQLE knockdown produced significant inhibition on cancer-related phenotypes of <t>U2OS</t> cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.
U2os, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+os+cell+lines+saos+2+htb+85/U-2+OS/pmc09980341-88-1-12
Average 98 stars, based on 1 article reviews
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96
ATCC homo sapiens bone osteosarcoma cells
SQLE knockdown produced significant inhibition on cancer-related phenotypes of <t>U2OS</t> cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.
Homo Sapiens Bone Osteosarcoma Cells, 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/product/human+os+cell+lines+saos+2+htb+85/Homo+sapiens/pmc07277215-157-9-15
Average 96 stars, based on 1 article reviews
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99
ATCC human tumor cell lines
SQLE knockdown produced significant inhibition on cancer-related phenotypes of <t>U2OS</t> cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.
Human Tumor Cell Lines, 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/human+os+cell+lines+saos+2+htb+85/U-87+MG/pmc00521140-28-0-24
Average 99 stars, based on 1 article reviews
human tumor cell lines - by Bioz Stars, 2026-09
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96
ATCC human osteosarcoma cells
SQLE knockdown produced significant inhibition on cancer-related phenotypes of <t>U2OS</t> cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.
Human Osteosarcoma Cells, 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/product/human+os+cell+lines+saos+2+htb+85/Soybean+Trypsin+Inhibitor/pmc09007416-87-0-4
Average 96 stars, based on 1 article reviews
human osteosarcoma cells - by Bioz Stars, 2026-09
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cells  (ATCC)
98
ATCC cells
SQLE knockdown produced significant inhibition on cancer-related phenotypes of <t>U2OS</t> cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.
Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+os+cell+lines+saos+2+htb+85/PC-12/pm31945187-53-19-24
Average 98 stars, based on 1 article reviews
cells - by Bioz Stars, 2026-09
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96
ATCC human osteosarcoma saosi2 cell line
SQLE knockdown produced significant inhibition on cancer-related phenotypes of <t>U2OS</t> cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.
Human Osteosarcoma Saosi2 Cell Line, 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/product/human+os+cell+lines+saos+2+htb+85/Malme-3%3B+Skin+Fibroblast%3B+Human/pm08964842-110-10-17
Average 96 stars, based on 1 article reviews
human osteosarcoma saosi2 cell line - by Bioz Stars, 2026-09
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97
ATCC 143b crl 8303 cells
Number of differentially regulated genes enriched in KEGG pathways after serial passaging of indicated cell lines.
143b Crl 8303 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+os+cell+lines+saos+2+htb+85/143B/pmc04438062-49-6-12
Average 97 stars, based on 1 article reviews
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99
ATCC human os cell lines
Number of differentially regulated genes enriched in KEGG pathways after serial passaging of indicated cell lines.
Human Os Cell Lines, 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/human+os+cell+lines+saos+2+htb+85/U-2+OS/pmc04567063-53-10-15
Average 99 stars, based on 1 article reviews
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saos 2  (ATCC)
99
ATCC saos 2
Number of differentially regulated genes enriched in KEGG pathways after serial passaging of indicated cell lines.
Saos 2, 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/human+os+cell+lines+saos+2+htb+85/293%3B+Embryonic+Kidney%3B+Human/us07321074-290-30-31
Average 99 stars, based on 1 article reviews
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Image Search Results


SQLE knockdown produced significant inhibition on cancer-related phenotypes of U2OS cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.

Journal: Frontiers in Oncology

Article Title: Molecular features and predictive models identify the most lethal subtype and a therapeutic target for osteosarcoma

doi: 10.3389/fonc.2023.1111570

Figure Lengend Snippet: SQLE knockdown produced significant inhibition on cancer-related phenotypes of U2OS cells in vitro . (A) Quantitative PCR (Q−PCR) with mRNA expression confirmed the knockdown of SQLE after 24h siRNA transfection. (B) Western blot analyses with protein expression confirmed the knockdown of SQLE after 48h siRNA transfection. The β-actin was treated as the loading control. (C) Cell proliferation was suppressed by SQLE knockdown. (D) Cell colony formation ability was reduced by SQLE knockdown. (E) Cell migration was inhibited by SQLE knockdown. The scale bar represented 100 μm. (F) and (G) indicated the quantification of positive signals from (D, E) , respectively. (H) The knockdown of SQLE significantly reduced the intracellular cholesterol. Error bars represented ± SD of three biological replicates. **P < 0.01, ***P < 0.001 by Student t-test.

Article Snippet: The U2OS and Saos-2, human osteosarcoma cell lines, were obtained from the American Type Culture Collection (ATCC, VA, USA).

Techniques: Produced, Inhibition, In Vitro, Real-time Polymerase Chain Reaction, Expressing, Transfection, Western Blot, Migration

Terbinafine treatment impaired the growth and migration of U2OS cells in vitro . (A) Different gradient concentrations of terbinafine were added to the U2OS cells. As the dosage of terbinafine increased, the viability of the cells decreased. (B) The U2OS cells were respectively treated with 25 μM and 50 μM terbinafine. Cell colony formation ability was found reduced with the increasing dosage of terbinafine. (C) The number of migrating cells decreased obviously with the increase in drug concentration. Scale bars, 100 μm. (D, E) indicated the quantification of positive signals from (B, C) , respectively. (F) The terbinafine treatment significantly reduced the intracellular cholesterol. Error bars represent mean ± SD; statistical analysis was performed using the Student t-test. **P < 0.01, ***P < 0.001.

Journal: Frontiers in Oncology

Article Title: Molecular features and predictive models identify the most lethal subtype and a therapeutic target for osteosarcoma

doi: 10.3389/fonc.2023.1111570

Figure Lengend Snippet: Terbinafine treatment impaired the growth and migration of U2OS cells in vitro . (A) Different gradient concentrations of terbinafine were added to the U2OS cells. As the dosage of terbinafine increased, the viability of the cells decreased. (B) The U2OS cells were respectively treated with 25 μM and 50 μM terbinafine. Cell colony formation ability was found reduced with the increasing dosage of terbinafine. (C) The number of migrating cells decreased obviously with the increase in drug concentration. Scale bars, 100 μm. (D, E) indicated the quantification of positive signals from (B, C) , respectively. (F) The terbinafine treatment significantly reduced the intracellular cholesterol. Error bars represent mean ± SD; statistical analysis was performed using the Student t-test. **P < 0.01, ***P < 0.001.

Article Snippet: The U2OS and Saos-2, human osteosarcoma cell lines, were obtained from the American Type Culture Collection (ATCC, VA, USA).

Techniques: Migration, In Vitro, Concentration Assay

Number of differentially regulated genes enriched in KEGG pathways after serial passaging of indicated cell lines.

Journal: PLoS ONE

Article Title: Genomic Instability of Osteosarcoma Cell Lines in Culture: Impact on the Prediction of Metastasis Relevant Genes

doi: 10.1371/journal.pone.0125611

Figure Lengend Snippet: Number of differentially regulated genes enriched in KEGG pathways after serial passaging of indicated cell lines.

Article Snippet: Human SAOS (HTB-85), HOS (CRL-1543) and 143B (CRL-8303) cells were obtained from ATCC (Rockville, MD).

Techniques: Passaging

Number of differentially regulated genes enriched in KEGG pathways in high and low metastatic cell lines.

Journal: PLoS ONE

Article Title: Genomic Instability of Osteosarcoma Cell Lines in Culture: Impact on the Prediction of Metastasis Relevant Genes

doi: 10.1371/journal.pone.0125611

Figure Lengend Snippet: Number of differentially regulated genes enriched in KEGG pathways in high and low metastatic cell lines.

Article Snippet: Human SAOS (HTB-85), HOS (CRL-1543) and 143B (CRL-8303) cells were obtained from ATCC (Rockville, MD).

Techniques:

Indicated genes are up-regulated (>2-fold; p<0.05) in at least three passage comparisons. Genes up-regulated in four passage comparisons are shown in bold. Genes marked in red are up-regulated in all three metastatic cell lines. Genes marked in purple, blue and green are shared by LM5 and LM8, LM5 and143B and LM8 and 143B, respectively.

Journal: PLoS ONE

Article Title: Genomic Instability of Osteosarcoma Cell Lines in Culture: Impact on the Prediction of Metastasis Relevant Genes

doi: 10.1371/journal.pone.0125611

Figure Lengend Snippet: Indicated genes are up-regulated (>2-fold; p<0.05) in at least three passage comparisons. Genes up-regulated in four passage comparisons are shown in bold. Genes marked in red are up-regulated in all three metastatic cell lines. Genes marked in purple, blue and green are shared by LM5 and LM8, LM5 and143B and LM8 and 143B, respectively.

Article Snippet: Human SAOS (HTB-85), HOS (CRL-1543) and 143B (CRL-8303) cells were obtained from ATCC (Rockville, MD).

Techniques: