tumor spheroid formation medium cat Search Results


mda mb 361  (ATCC)
97
ATCC mda mb 361
Mda Mb 361, 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
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mda mb 361 - by Bioz Stars, 2026-03
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def cs xeno free 3d spheroid culture medium  (TaKaRa)
95
TaKaRa def cs xeno free 3d spheroid culture medium
Def Cs Xeno Free 3d Spheroid Culture Medium, supplied by TaKaRa, 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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Average 95 stars, based on 1 article reviews
def cs xeno free 3d spheroid culture medium - by Bioz Stars, 2026-03
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pneumacult-ex plus  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc pneumacult-ex plus
Pneumacult Ex Plus, supplied by STEMCELL Technologies 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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pneumacult-ex plus - by Bioz Stars, 2026-03
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aale  (Lonza)
90
Lonza aale
Aale, 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
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aale - by Bioz Stars, 2026-03
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tumor spheroid formation medium cat#20141-500  (ProMab Inc)
90
ProMab Inc tumor spheroid formation medium cat#20141-500
The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid <t>formation</t> assay to assess the single-cell derived <t>tumor-spheroid</t> formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.
Tumor Spheroid Formation Medium Cat#20141 500, supplied by ProMab 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/result/tumor spheroid formation medium cat#20141-500/product/ProMab Inc
Average 90 stars, based on 1 article reviews
tumor spheroid formation medium cat#20141-500 - by Bioz Stars, 2026-03
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rpmi-1640 medium  (Thermo Fisher)
90
Thermo Fisher rpmi-1640 medium
The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid <t>formation</t> assay to assess the single-cell derived <t>tumor-spheroid</t> formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.
Rpmi 1640 Medium, supplied by Thermo Fisher, 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/rpmi-1640 medium/product/Thermo Fisher
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mercaptoethanol cat 21985 023 gibco cell culture mouse lymphoma tumor cells eg7 ova were cultured in rpmi 1640 medium supplemented  (Thermo Fisher)
99
Thermo Fisher mercaptoethanol cat 21985 023 gibco cell culture mouse lymphoma tumor cells eg7 ova were cultured in rpmi 1640 medium supplemented
The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid <t>formation</t> assay to assess the single-cell derived <t>tumor-spheroid</t> formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.
Mercaptoethanol Cat 21985 023 Gibco Cell Culture Mouse Lymphoma Tumor Cells Eg7 Ova Were Cultured In Rpmi 1640 Medium Supplemented, supplied by Thermo Fisher, 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/result/mercaptoethanol cat 21985 023 gibco cell culture mouse lymphoma tumor cells eg7 ova were cultured in rpmi 1640 medium supplemented/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
mercaptoethanol cat 21985 023 gibco cell culture mouse lymphoma tumor cells eg7 ova were cultured in rpmi 1640 medium supplemented - by Bioz Stars, 2026-03
99/100 stars
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tnf α  (InvivoGen)
95
InvivoGen tnf α
The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid <t>formation</t> assay to assess the single-cell derived <t>tumor-spheroid</t> formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.
Tnf α, supplied by InvivoGen, 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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Average 95 stars, based on 1 article reviews
tnf α - by Bioz Stars, 2026-03
95/100 stars
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spheroid spin media bioivt invitrogro spheroid spin medium  (BioIVT Inc)
90
BioIVT Inc spheroid spin media bioivt invitrogro spheroid spin medium
The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid <t>formation</t> assay to assess the single-cell derived <t>tumor-spheroid</t> formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.
Spheroid Spin Media Bioivt Invitrogro Spheroid Spin Medium, supplied by BioIVT 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/result/spheroid spin media bioivt invitrogro spheroid spin medium/product/BioIVT Inc
Average 90 stars, based on 1 article reviews
spheroid spin media bioivt invitrogro spheroid spin medium - by Bioz Stars, 2026-03
90/100 stars
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rpmi 1640 medium  (Thermo Fisher)
90
Thermo Fisher rpmi 1640 medium
The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid <t>formation</t> assay to assess the single-cell derived <t>tumor-spheroid</t> formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.
Rpmi 1640 Medium, supplied by Thermo Fisher, 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/rpmi 1640 medium/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
rpmi 1640 medium - by Bioz Stars, 2026-03
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high ca125 control sera  (Bio-Rad)
92
Bio-Rad high ca125 control sera
OC Test and <t>CA125</t> enzyme-linked immunosorbent assay performance in healthy controls and in ovarian cancers. A and C: Training study EDTA plasma samples are shown. B and D : The verification study serum samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph. HGSC, high-grade serous carcinoma; LGSC, low-grade serous carcinoma.
High Ca125 Control Sera, supplied by Bio-Rad, 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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Average 92 stars, based on 1 article reviews
high ca125 control sera - by Bioz Stars, 2026-03
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human gm-csf  (PeproTech)
90
PeproTech human gm-csf
OC Test and <t>CA125</t> enzyme-linked immunosorbent assay performance in healthy controls and in ovarian cancers. A and C: Training study EDTA plasma samples are shown. B and D : The verification study serum samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph. HGSC, high-grade serous carcinoma; LGSC, low-grade serous carcinoma.
Human Gm Csf, supplied by PeproTech, 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


The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid formation assay to assess the single-cell derived tumor-spheroid formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.

Journal: Frontiers in Cell and Developmental Biology

Article Title: PIP5K1α is Required for Promoting Tumor Progression in Castration-Resistant Prostate Cancer

doi: 10.3389/fcell.2022.798590

Figure Lengend Snippet: The effect of N-terminal-truncated PIP5K1α on the proliferation and migratory ability of PIP5K1αΔN C4-2 cells. (A) Immunoblot analysis on the expression of trunctated PIP5K1α in PIP5K1αΔN C4-2 cells (PIP5K1αΔN) or full-length PIP5K1α in SG C4-2 cells (SG) is shown. The antibody against full-length PIP5K1α was used. Quantification of the expression level of PIP5K1αΔN and PIP5K1α in the cells is shown. (B) Representative image of the quantitative RT-PCR to show mRNA expression of WT PIP5K1A and truncated PIP5K1A in SG cells and in PIP5K1αΔN cells, respectively. (C) Immunoblot analysis on the expression of PIP5K1α and PIP5K1αΔN in SG cells and PIP5K1αΔN cells that were treated with MG132 or vehicle control. Quantifications of the immunoblots for expression of PIP5K1αΔN and PIP5K1α are shown in the right panel. (D) Non-radioactive MTS reagent was used to measure the proliferation rate of SG cells and PIP5K1αΔN cells. (E) SG cells and PIP5K1αΔN cells were subjected to the trans-well Boyden chamber migration assays. The relative counts of the migrated cells are shown. (F) SG cells and PIP5K1αΔN cells were subjected to the tumorspheroid formation assay to assess the single-cell derived tumor-spheroid formation and growth. Representative images of tumor-spheroids derived from SG cells and PIP5K1αΔN cells are shown. The relative counts of tumor spheroids from each group are shown. Data in this figure is presented as the average of three independent experiments (±SE). Student’s t -test was used in the analysis. ** p < 0.01 is indicated.

Article Snippet: PCa cells were made in single-cell suspensions and 1 × 10 5 cells were cultured in suspension in 2 ml of tumor spheroid formation medium (Cat#20141-500, promab Cancer Stem PremiumTM).

Techniques: Western Blot, Expressing, Quantitative RT-PCR, Control, Migration, Tube Formation Assay, Derivative Assay

OC Test and CA125 enzyme-linked immunosorbent assay performance in healthy controls and in ovarian cancers. A and C: Training study EDTA plasma samples are shown. B and D : The verification study serum samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph. HGSC, high-grade serous carcinoma; LGSC, low-grade serous carcinoma.

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: Improving Specificity for Ovarian Cancer Screening Using a Novel Extracellular Vesicle–Based Blood Test

doi: 10.1016/j.jmoldx.2024.09.001

Figure Lengend Snippet: OC Test and CA125 enzyme-linked immunosorbent assay performance in healthy controls and in ovarian cancers. A and C: Training study EDTA plasma samples are shown. B and D : The verification study serum samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph. HGSC, high-grade serous carcinoma; LGSC, low-grade serous carcinoma.

Article Snippet: Blinded human plasma and serum samples as well as Lyphochek Tumor Marker Plus low, medium, and high CA125 control sera (catalog number 548X; Bio-Rad, Hercules, CA) were diluted 1:10 in 1× phosphate-buffered saline, pH 7.4 (Gibco catalog number 10010023; Thermo Fisher Scientific).

Techniques: Enzyme-linked Immunosorbent Assay, Clinical Proteomics

Comparison of the Sensitivity of the OC Test and CA125 by Ovarian Cancer Histotype and Stage in the Verification Study

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: Improving Specificity for Ovarian Cancer Screening Using a Novel Extracellular Vesicle–Based Blood Test

doi: 10.1016/j.jmoldx.2024.09.001

Figure Lengend Snippet: Comparison of the Sensitivity of the OC Test and CA125 by Ovarian Cancer Histotype and Stage in the Verification Study

Article Snippet: Blinded human plasma and serum samples as well as Lyphochek Tumor Marker Plus low, medium, and high CA125 control sera (catalog number 548X; Bio-Rad, Hercules, CA) were diluted 1:10 in 1× phosphate-buffered saline, pH 7.4 (Gibco catalog number 10010023; Thermo Fisher Scientific).

Techniques: Comparison

OC Test and CA125 enzyme-linked immunosorbent assay performance in benign ovarian conditions. A and C: Training study EDTA plasma samples are shown. B and D: The verification study serum samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph.

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: Improving Specificity for Ovarian Cancer Screening Using a Novel Extracellular Vesicle–Based Blood Test

doi: 10.1016/j.jmoldx.2024.09.001

Figure Lengend Snippet: OC Test and CA125 enzyme-linked immunosorbent assay performance in benign ovarian conditions. A and C: Training study EDTA plasma samples are shown. B and D: The verification study serum samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph.

Article Snippet: Blinded human plasma and serum samples as well as Lyphochek Tumor Marker Plus low, medium, and high CA125 control sera (catalog number 548X; Bio-Rad, Hercules, CA) were diluted 1:10 in 1× phosphate-buffered saline, pH 7.4 (Gibco catalog number 10010023; Thermo Fisher Scientific).

Techniques: Enzyme-linked Immunosorbent Assay, Clinical Proteomics

Comparison of the Performance of the OC Test and CA125 in Nonovarian Cancers and Inflammatory Conditions

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: Improving Specificity for Ovarian Cancer Screening Using a Novel Extracellular Vesicle–Based Blood Test

doi: 10.1016/j.jmoldx.2024.09.001

Figure Lengend Snippet: Comparison of the Performance of the OC Test and CA125 in Nonovarian Cancers and Inflammatory Conditions

Article Snippet: Blinded human plasma and serum samples as well as Lyphochek Tumor Marker Plus low, medium, and high CA125 control sera (catalog number 548X; Bio-Rad, Hercules, CA) were diluted 1:10 in 1× phosphate-buffered saline, pH 7.4 (Gibco catalog number 10010023; Thermo Fisher Scientific).

Techniques: Comparison

OC Test and CA125 enzyme-linked immunosorbent assay performance in nonovarian cancers and inflammatory conditions. A and C: Nonovarian (off-target cancer) samples are shown. B and D: The inflammatory condition samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph.

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: Improving Specificity for Ovarian Cancer Screening Using a Novel Extracellular Vesicle–Based Blood Test

doi: 10.1016/j.jmoldx.2024.09.001

Figure Lengend Snippet: OC Test and CA125 enzyme-linked immunosorbent assay performance in nonovarian cancers and inflammatory conditions. A and C: Nonovarian (off-target cancer) samples are shown. B and D: The inflammatory condition samples are shown. The cutoff set between healthy controls and OC cases is shown as a red dotted line in each graph.

Article Snippet: Blinded human plasma and serum samples as well as Lyphochek Tumor Marker Plus low, medium, and high CA125 control sera (catalog number 548X; Bio-Rad, Hercules, CA) were diluted 1:10 in 1× phosphate-buffered saline, pH 7.4 (Gibco catalog number 10010023; Thermo Fisher Scientific).

Techniques: Enzyme-linked Immunosorbent Assay

Estimated Rates of False Positives due to Nonovarian Cancers if the OC Test or CA125 Was to Be Used for Screening an Average Risk Population

Journal: The Journal of Molecular Diagnostics : JMD

Article Title: Improving Specificity for Ovarian Cancer Screening Using a Novel Extracellular Vesicle–Based Blood Test

doi: 10.1016/j.jmoldx.2024.09.001

Figure Lengend Snippet: Estimated Rates of False Positives due to Nonovarian Cancers if the OC Test or CA125 Was to Be Used for Screening an Average Risk Population

Article Snippet: Blinded human plasma and serum samples as well as Lyphochek Tumor Marker Plus low, medium, and high CA125 control sera (catalog number 548X; Bio-Rad, Hercules, CA) were diluted 1:10 in 1× phosphate-buffered saline, pH 7.4 (Gibco catalog number 10010023; Thermo Fisher Scientific).

Techniques: