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94
CLS Cell Lines Service GmbH a549
A549, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CLS Cell Lines Service GmbH hacat cells
Hacat Cells, supplied by CLS Cell Lines Service GmbH, 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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CLS Cell Lines Service GmbH ovcar 3 cells
Ovcar 3 Cells, supplied by CLS Cell Lines Service GmbH, 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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CLS Cell Lines Service GmbH cell lines hdpscs human dental pulp stem cells 300 702 and hgfs human gingival fibroblasts 300 703
Cell Lines Hdpscs Human Dental Pulp Stem Cells 300 702 And Hgfs Human Gingival Fibroblasts 300 703, supplied by CLS Cell Lines Service GmbH, 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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CLS Cell Lines Service GmbH research cell line source s huh7 cells
Research Cell Line Source S Huh7 Cells, supplied by CLS Cell Lines Service GmbH, 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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CLS Cell Lines Service GmbH panc02 cells
Panc02 Cells, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CLS Cell Lines Service GmbH human cytion cat
Human Cytion Cat, supplied by CLS Cell Lines Service GmbH, 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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CLS Cell Lines Service GmbH adherent mx
Adherent Mx, supplied by CLS Cell Lines Service GmbH, 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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CLS Cell Lines Service GmbH lncap
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Lncap, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CLS Cell Lines Service GmbH nup96 snap cells
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Nup96 Snap Cells, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
CLS Cell Lines Service GmbH accutase
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Accutase, supplied by CLS Cell Lines Service GmbH, 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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92
CLS Cell Lines Service GmbH hep 55 1
NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a <t>),</t> <t>OVCAR-3</t> ( b ), <t>LNCaP</t> ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.
Hep 55 1, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP-induced alterations in extracellular H 2 O 2 levels, intracellular ROS production, and MMP in tumor cells. ( A ): H 2 O 2 level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( a ); NO 2 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( b ); NO 3 − level in the cell culture medium RPMI 1640 and DMEM/F12, and PBS after treatment with NIPP ( c ). ( B ): ROS level inside the tumor cells SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells, after treatment with the NIPP in 30 min ( n = 6). All data are normalized to the control group; ( C ): Mitochondria membrane potential relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), MDA-MB-231 ( f ) cells after the exposure of NIPP 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. All data are normalized to the control group. *** p < 0.001, **: p < 0.01, *: p < 0.05.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Cell Culture, Control, Membrane

NIPP inhibits the proliferation of tumor cells. ( A ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were categorized based on their distance from NIPP to the medium surface: the control group, 1 cm group, 3 cm group, and 6 cm group. All groups, except the control group, were exposed to NIPP for 4 min. Each experiment was conducted at least three times. ( B ): Visualization of NIPP treatment tumor cells with different distances. ( C ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were organized based on the treatment time of NIPP for the tumor cells: the control group, 1 min group, 2 min group, and 4 min group. Except for the control group, the distance of NIPP from the culture medium was 1 cm for all groups. ( D ): Visualization of NIPP treatment tumor cells with different duration. Each experiment was repeated at least three times. ( E ): Wound-healing Test of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells at 0 and 24 h. Each experimental group was compared with the control group.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP inhibits the proliferation of tumor cells. ( A ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were categorized based on their distance from NIPP to the medium surface: the control group, 1 cm group, 3 cm group, and 6 cm group. All groups, except the control group, were exposed to NIPP for 4 min. Each experiment was conducted at least three times. ( B ): Visualization of NIPP treatment tumor cells with different distances. ( C ): Cell growth curves for SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. The groups were organized based on the treatment time of NIPP for the tumor cells: the control group, 1 min group, 2 min group, and 4 min group. Except for the control group, the distance of NIPP from the culture medium was 1 cm for all groups. ( D ): Visualization of NIPP treatment tumor cells with different duration. Each experiment was repeated at least three times. ( E ): Wound-healing Test of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells at 0 and 24 h. Each experimental group was compared with the control group.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Control

NIPP treatment alters the cytoskeletal organization of tumor cells and glucose consumption in tumor cell culture medium. ( A ): Immunofluorescence of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. Green represents F-actin, and Blue represents the Nucleus. Magnification 20×. Next row of pictures are partial screenshots from the previous row. ( B ): Glucose relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( C ): Lactate relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP treatment alters the cytoskeletal organization of tumor cells and glucose consumption in tumor cell culture medium. ( A ): Immunofluorescence of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells. Green represents F-actin, and Blue represents the Nucleus. Magnification 20×. Next row of pictures are partial screenshots from the previous row. ( B ): Glucose relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( C ): Lactate relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h, 48 h, and 72 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Cell Culture, Immunofluorescence, Control

NIPP increases LDH release in tumor cell cultures and induced no significante alterations of SOD levels in tumor cell. ( A ): LDH relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 30 min and 24 h. ( B ): SOD relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: NIPP increases LDH release in tumor cell cultures and induced no significante alterations of SOD levels in tumor cell. ( A ): LDH relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 30 min and 24 h. ( B ): SOD relative level in the medium of SKOV-3 ( a ), OVCAR-3 ( b ), LNCaP ( c ), PC-3 ( d ), MCF-7 ( e ), and MDA-MB-231 ( f ) cells after the exposure to NIPP for 24 h. Every experiment was replicated at least 3 times. Each experimental group was compared with the control group. ***: p < 0.001, **: p < 0.01, *: p < 0.05.

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Control

( A ): Quantification of HSP27 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP27 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP40 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP40 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP70 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP70 relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7, and MDA-MB-231 cells after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP90α relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP90α relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control

( A ): Quantification of HSP90β relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Journal: Cancers

Article Title: Non-Invasive Physical Plasma as an Oncological Therapy Option: Modulation of Cancer Cell Growth, Motility, and Metabolism Without Induction of Cancer Resistance Factors

doi: 10.3390/cancers17213517

Figure Lengend Snippet: ( A ): Quantification of HSP90β relative expression level in SKOV-3, OVCAR-3, LNCaP, PC-3, MCF-7 cells, and MDA-MB-231 after the exposure to NIPP for 24 h, 48 h, and 72 h. ( B ): Western blot signals. Each experiment was replicated at least 3 times. Experimental groups were compared to control group. They were statistically evaluated with Student t -test. **: p < 0.01, *: p < 0.05. The uncropped bolts are shown in .

Article Snippet: SKOV-3 (Cryovial: 300343, Cell Lines Service GmbH, Heidelberg, Germany), OVCAR-3 (Cryovial: 300307, Cell Lines Service GmbH, Heidelberg, Germany), LNCaP (Cryovial:300265, Cell Lines Service GmbH, Heidelberg, Germany), PC-3 (Cryovial: 300312, Cell Lines Service GmbH, Heidelberg, Germany), MCF-7 (Cryovial: 300273, Cell Lines Service GmbH, Heidelberg, Germany), and MDA-MB-231 (Cat. no.: EP-CL-0150, Elabscience Biotechnology Inc., Houston, TX, USA) cell lines were purchased, aliquoted, and stored frozen.

Techniques: Expressing, Western Blot, Control