breast cancer cell lines mda mb 231 Search Results


93
ATCC breast cancer cell line
Breast Cancer Cell Line, supplied by ATCC, 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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Genecopoeia luciferase gfp variants
Luciferase Gfp Variants, supplied by Genecopoeia, 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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93
OriGene human breast cancer cells mda mb
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Human Breast Cancer Cells Mda Mb, supplied by OriGene, 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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90
Cells Online LLC gfp expressing mda-mb-231 breast adenocarcinoma cell line
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Gfp Expressing Mda Mb 231 Breast Adenocarcinoma Cell Line, supplied by Cells Online LLC, 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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Average 90 stars, based on 1 article reviews
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90
EPO GmbH breast cancer cell line mda-mb-231
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Breast Cancer Cell Line Mda Mb 231, supplied by EPO GmbH, 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/breast cancer cell line mda-mb-231/product/EPO GmbH
Average 90 stars, based on 1 article reviews
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90
iCell Gene Therapeutics mda-mb-231 cell lines icell-h133
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Mda Mb 231 Cell Lines Icell H133, supplied by iCell Gene Therapeutics, 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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90
Cato Research cisplatin-resistant (mda/r) variants of the mda-mb-231 human breast cancer cell line
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Cisplatin Resistant (Mda/R) Variants Of The Mda Mb 231 Human Breast Cancer Cell Line, supplied by Cato Research, 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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Average 90 stars, based on 1 article reviews
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90
SRI International mefs
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Mefs, supplied by SRI International, 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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Average 90 stars, based on 1 article reviews
mefs - by Bioz Stars, 2026-02
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Genentech inc mda-mb231-x1.1 (gfp-expressing variant of mda-mb-231 cells) human breast carcinoma cells
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Mda Mb231 X1.1 (Gfp Expressing Variant Of Mda Mb 231 Cells) Human Breast Carcinoma Cells, supplied by Genentech inc, 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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SAURER Inc breast carcinoma cell line mda-mb 231
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Breast Carcinoma Cell Line Mda Mb 231, supplied by SAURER Inc, 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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90
Ubigene Biosciences Co Ltd breast cancer cell line mda-mb-231
PKC-ζ knockdown retards <t>invasion</t> <t>of</t> <t>MDA-MB-231</t> breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.
Breast Cancer Cell Line Mda Mb 231, supplied by Ubigene Biosciences Co Ltd, 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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Biologica Environmental Services human breast adenocarcinoma cell lines mda-mb-231 htl99004
Mean ± SD of resonant frequency, min|S 11 (f)|, full width at half maximum, and fitting error. n = 8.
Human Breast Adenocarcinoma Cell Lines Mda Mb 231 Htl99004, supplied by Biologica Environmental Services, 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


PKC-ζ knockdown retards invasion of MDA-MB-231 breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.

Journal: Oncology Letters

Article Title: Analysis of PKC-ζ protein levels in normal and malignant breast tissue subtypes

doi: 10.3892/ol.2018.9792

Figure Lengend Snippet: PKC-ζ knockdown retards invasion of MDA-MB-231 breast cancer cells. MDA-MB-231 breast cancer cells were placed in the upper chamber of Transwell plate coated with 0.5X BME and serum containing media was placed in the lower chamber as a chemoattractant. Following transfection with siPRKCZ and scrambled RNA, cells that invaded through the BME and migrated into the lower chamber were stained with crystal violet and (A) observed under a microscope at magnification, ×10; scale bar, 1 mm. Untreated cells and cells treated with the transfection reagent (Si-Tran) were also used to establish the effect on invasion. (B) The cells were counted for each treatment image ( N =3), averaged and analyzed with the standard deviation, a Student's t-test (*P<0.05) and a one-way ANOVA was also used to evaluate the data with the post-hoc Tukey's HSD test (P<0.01), Scheffé multiple comparison (P<0.01), Bonferroni (P<0.01) and Holm (P<0.01). All statistical tests were used to determine the statistical significance of the invasion data. (C) The cells were further investigated by western blot to analyze the Rac1/RhoA pathway. This data was quantified and averaged for the graph with standard error of the mean represented. PKC-ζ, protein kinase C-ζ; BME, basement membrane extract; Rac1, Ras-related C3 botulinum toxin substrate 1; RhoA, Ras homolog gene family member A.

Article Snippet: Human breast cancer cells MDA-MB-231 were grown in 100 mm plates and transfected with 20 nM of scrambled RNA and siPRKCZ (5′-GCAUGAUGACGAGGAUAUUGACUGG-3′, SR303747A; Origene, Rockville, MD, USA) for 48 h. Cells were lysed as previously described and the lysates were run on western blots.

Techniques: Transfection, Staining, Microscopy, Standard Deviation, Western Blot

Organization of F-actin upon the knockdown of PKC-ζ. MDA-MB-231 breast cancer cells were treated with SiTran, scrambled RNA and siPRKC-ζ for 24 h. The cells that received no treatment were used as the control. These cells were then stained with 1X Phalloidin-iFluor 594 and counterstained with DAPI. Scale bar, 100 µm. Original magnification, ×20. DAPI, 4′,6-diamidino-2-phenylindole; F-actin, filamentous actin; PKC-ζ, protein kinase C-ζ.

Journal: Oncology Letters

Article Title: Analysis of PKC-ζ protein levels in normal and malignant breast tissue subtypes

doi: 10.3892/ol.2018.9792

Figure Lengend Snippet: Organization of F-actin upon the knockdown of PKC-ζ. MDA-MB-231 breast cancer cells were treated with SiTran, scrambled RNA and siPRKC-ζ for 24 h. The cells that received no treatment were used as the control. These cells were then stained with 1X Phalloidin-iFluor 594 and counterstained with DAPI. Scale bar, 100 µm. Original magnification, ×20. DAPI, 4′,6-diamidino-2-phenylindole; F-actin, filamentous actin; PKC-ζ, protein kinase C-ζ.

Article Snippet: Human breast cancer cells MDA-MB-231 were grown in 100 mm plates and transfected with 20 nM of scrambled RNA and siPRKCZ (5′-GCAUGAUGACGAGGAUAUUGACUGG-3′, SR303747A; Origene, Rockville, MD, USA) for 48 h. Cells were lysed as previously described and the lysates were run on western blots.

Techniques: Staining

Mean ± SD of resonant frequency, min|S 11 (f)|, full width at half maximum, and fitting error. n = 8.

Journal: Sensors (Basel, Switzerland)

Article Title: A Novel Microwave Resonant Sensor for Measuring Cancer Cell Line Aggressiveness

doi: 10.3390/s22124383

Figure Lengend Snippet: Mean ± SD of resonant frequency, min|S 11 (f)|, full width at half maximum, and fitting error. n = 8.

Article Snippet: Pediatric human osteosarcoma cell line SaOS-2 (HTL01001), human breast adenocarcinoma cell lines MCF7 (HTL95021) and MDA-MB-231 (HTL99004) were purchased from Banca Biologica and Cell Factory (IRCCS Azienda Ospedaliera Universitaria San Martino-IST, Genova, Italy), while the pediatric osteosarcoma cell line 143B (CRL-8303) was purchased from the American Type Culture Collection (Manassas, VA, USA).

Techniques:

Resonant frequency values computed for pure DMEM, and the four tested cell lines: low-aggressive SaOS-2 and high-aggressive 143B osteosarcoma cell lines, and low-aggressive MCF7 and high-aggressive MDA-MB-231 breast cancer cell lines. n = 8. *, p < 0.05 and ****, p < 0.0001.

Journal: Sensors (Basel, Switzerland)

Article Title: A Novel Microwave Resonant Sensor for Measuring Cancer Cell Line Aggressiveness

doi: 10.3390/s22124383

Figure Lengend Snippet: Resonant frequency values computed for pure DMEM, and the four tested cell lines: low-aggressive SaOS-2 and high-aggressive 143B osteosarcoma cell lines, and low-aggressive MCF7 and high-aggressive MDA-MB-231 breast cancer cell lines. n = 8. *, p < 0.05 and ****, p < 0.0001.

Article Snippet: Pediatric human osteosarcoma cell line SaOS-2 (HTL01001), human breast adenocarcinoma cell lines MCF7 (HTL95021) and MDA-MB-231 (HTL99004) were purchased from Banca Biologica and Cell Factory (IRCCS Azienda Ospedaliera Universitaria San Martino-IST, Genova, Italy), while the pediatric osteosarcoma cell line 143B (CRL-8303) was purchased from the American Type Culture Collection (Manassas, VA, USA).

Techniques:

Min|S 11 (f)| ( a ) and FWHM ( b ) computed for pure DMEM, and the four tested cell lines: low-aggressive SaOS-2 and high-aggressive 143B osteosarcoma cell lines, and low-aggressive MCF7 and high-aggressive MDA-MB-231 breast cancer cell lines. n = 8.

Journal: Sensors (Basel, Switzerland)

Article Title: A Novel Microwave Resonant Sensor for Measuring Cancer Cell Line Aggressiveness

doi: 10.3390/s22124383

Figure Lengend Snippet: Min|S 11 (f)| ( a ) and FWHM ( b ) computed for pure DMEM, and the four tested cell lines: low-aggressive SaOS-2 and high-aggressive 143B osteosarcoma cell lines, and low-aggressive MCF7 and high-aggressive MDA-MB-231 breast cancer cell lines. n = 8.

Article Snippet: Pediatric human osteosarcoma cell line SaOS-2 (HTL01001), human breast adenocarcinoma cell lines MCF7 (HTL95021) and MDA-MB-231 (HTL99004) were purchased from Banca Biologica and Cell Factory (IRCCS Azienda Ospedaliera Universitaria San Martino-IST, Genova, Italy), while the pediatric osteosarcoma cell line 143B (CRL-8303) was purchased from the American Type Culture Collection (Manassas, VA, USA).

Techniques: