bt474 cells Search Results


93
CLS Cell Lines Service GmbH bt474 cells
Effect of magnetic thermoablation on the BCL2, HSP70, and FGF-R1 protein expression pattern in <t>BT474</t> tumors. Notes: Representative pictures after IHC staining of BCL2, HSP70, and FGF-R1 were chosen. Blue: nuclei, red: protein-specific antibody, scale bar: 100 μm. Relative semi-quantitative expression of investigated proteins is depicted in diagrams. In diagrams, bars represent the relative number of slides with a specific protein expression normalized to the total number of all slides in the specific treatment group. Bar colors represent the amount of specifically stained area within the viable tumor region: unstained/negative (light gray), less than 50% of vital area stained (dark grey), more than 50% of vital area stained (black). Whereas a downregulation of BCL2 and FGF-R1 can be assumed, HSP70 expression remained unchanged. Abbreviations: BCL2, B-cell lymphoma 2; HSP70, heat shock protein; FGF-R1, fibroblast growth factor receptor 1; IHC, immunohistochemistry; MNP, magnetic nanoparticles; AMF, alternating magnetic field.
Bt474 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
https://www.bioz.com/product/bt474+cells/pmc04364160-32-18-22?v=CLS+Cell+Lines+Service+GmbH
Average 93 stars, based on 1 article reviews
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Elabscience Biotechnology bt 474 cells
Effect of magnetic thermoablation on the BCL2, HSP70, and FGF-R1 protein expression pattern in <t>BT474</t> tumors. Notes: Representative pictures after IHC staining of BCL2, HSP70, and FGF-R1 were chosen. Blue: nuclei, red: protein-specific antibody, scale bar: 100 μm. Relative semi-quantitative expression of investigated proteins is depicted in diagrams. In diagrams, bars represent the relative number of slides with a specific protein expression normalized to the total number of all slides in the specific treatment group. Bar colors represent the amount of specifically stained area within the viable tumor region: unstained/negative (light gray), less than 50% of vital area stained (dark grey), more than 50% of vital area stained (black). Whereas a downregulation of BCL2 and FGF-R1 can be assumed, HSP70 expression remained unchanged. Abbreviations: BCL2, B-cell lymphoma 2; HSP70, heat shock protein; FGF-R1, fibroblast growth factor receptor 1; IHC, immunohistochemistry; MNP, magnetic nanoparticles; AMF, alternating magnetic field.
Bt 474 Cells, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bt474+cells/pmc11509994-206-8-22?v=Elabscience+Biotechnology
Average 92 stars, based on 1 article reviews
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90
Becton Dickinson bt474 cells
DOTA-PNA-Peptide Cu-64 radiolabeling and <t> BT474 </t> Cellular Uptake
Bt474 Cells, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bt474+cells/pmc05842439-129-11-24?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
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90
National Centre for Cell Science bt-474 tumor cell line
DOTA-PNA-Peptide Cu-64 radiolabeling and <t> BT474 </t> Cellular Uptake
Bt 474 Tumor Cell Line, supplied by National Centre for Cell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bt474+cells/10__1002_slash_slct__202404451-253-3-12?v=National+Centre+for+Cell+Science
Average 90 stars, based on 1 article reviews
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China Center for Type Culture Collection bt-474
DOTA-PNA-Peptide Cu-64 radiolabeling and <t> BT474 </t> Cellular Uptake
Bt 474, supplied by China Center for Type Culture Collection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bt474+cells/pmc06694677-72-3-28?v=China+Center+for+Type+Culture+Collection
Average 90 stars, based on 1 article reviews
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AstraZeneca ltd bt474 cells
DOTA-PNA-Peptide Cu-64 radiolabeling and <t> BT474 </t> Cellular Uptake
Bt474 Cells, supplied by AstraZeneca ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bt474+cells/10__1158_slash_0008___5472__can___20___1847-45-4-15?v=AstraZeneca+ltd
Average 90 stars, based on 1 article reviews
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iCell Gene Therapeutics mda-mb-231 cell lines icell-h133
DOTA-PNA-Peptide Cu-64 radiolabeling and <t> BT474 </t> Cellular Uptake
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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Average 90 stars, based on 1 article reviews
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Caltag-Medsystems ltd bt474 cells
Endosomal recycling inhibitors downregulate ER-α and AR. A Heatmap displaying the top 30 hits from the RPPA analysis of control and 10 µM PQ-treated <t>BT474</t> cells (mean of two biological replicates; * indicates AR and ER-α). B Lysates of BT474 cells treated with 10 µM PQ for 24 h were immunoblotted with the indicated antibodies. Quantitative analysis of the fold difference of hormone receptor protein levels relative to control untreated cells indicated in the histogram ( n = 3–4). MDA-MB-134 VI ( C ) and SUM44-PE ( D ) invasive lobular breast carcinoma cells were treated with the indicated concentrations of PQ for 24 h prior to lysis and immunoblotting. Histograms indicate the fold change in ER-α protein levels relative to untreated cells ( n = 4). E MCF-7 cells were treated with the indicated concentrations of PQ and MON for 24 h. Lysates were immunoblotted with ER-α and AR antibodies, and the histogram indicates the fold difference in protein levels relative to untreated cells ( n = 3)
Bt474 Cells, supplied by Caltag-Medsystems ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bt474+cells/pmc10959794-82-1-6?v=Caltag-Medsystems+ltd
Average 90 stars, based on 1 article reviews
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Multiplexion GmbH human cell lines bt474 and a431
Endosomal recycling inhibitors downregulate ER-α and AR. A Heatmap displaying the top 30 hits from the RPPA analysis of control and 10 µM PQ-treated <t>BT474</t> cells (mean of two biological replicates; * indicates AR and ER-α). B Lysates of BT474 cells treated with 10 µM PQ for 24 h were immunoblotted with the indicated antibodies. Quantitative analysis of the fold difference of hormone receptor protein levels relative to control untreated cells indicated in the histogram ( n = 3–4). MDA-MB-134 VI ( C ) and SUM44-PE ( D ) invasive lobular breast carcinoma cells were treated with the indicated concentrations of PQ for 24 h prior to lysis and immunoblotting. Histograms indicate the fold change in ER-α protein levels relative to untreated cells ( n = 4). E MCF-7 cells were treated with the indicated concentrations of PQ and MON for 24 h. Lysates were immunoblotted with ER-α and AR antibodies, and the histogram indicates the fold difference in protein levels relative to untreated cells ( n = 3)
Human Cell Lines Bt474 And A431, supplied by Multiplexion 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/product/bt474+cells/10__1158_slash_1535___7163__mct___13___0288-63-6-14?v=Multiplexion+GmbH
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human cell lines bt474 and a431 - by Bioz Stars, 2026-07
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90
Biochrom bt-474 cells
Endosomal recycling inhibitors downregulate ER-α and AR. A Heatmap displaying the top 30 hits from the RPPA analysis of control and 10 µM PQ-treated <t>BT474</t> cells (mean of two biological replicates; * indicates AR and ER-α). B Lysates of BT474 cells treated with 10 µM PQ for 24 h were immunoblotted with the indicated antibodies. Quantitative analysis of the fold difference of hormone receptor protein levels relative to control untreated cells indicated in the histogram ( n = 3–4). MDA-MB-134 VI ( C ) and SUM44-PE ( D ) invasive lobular breast carcinoma cells were treated with the indicated concentrations of PQ for 24 h prior to lysis and immunoblotting. Histograms indicate the fold change in ER-α protein levels relative to untreated cells ( n = 4). E MCF-7 cells were treated with the indicated concentrations of PQ and MON for 24 h. Lysates were immunoblotted with ER-α and AR antibodies, and the histogram indicates the fold difference in protein levels relative to untreated cells ( n = 3)
Bt 474 Cells, supplied by Biochrom, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bt474+cells/pmc06542668-401-1-14?v=Biochrom
Average 90 stars, based on 1 article reviews
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90
Genolytic GmbH bt474 cells
Endosomal recycling inhibitors downregulate ER-α and AR. A Heatmap displaying the top 30 hits from the RPPA analysis of control and 10 µM PQ-treated <t>BT474</t> cells (mean of two biological replicates; * indicates AR and ER-α). B Lysates of BT474 cells treated with 10 µM PQ for 24 h were immunoblotted with the indicated antibodies. Quantitative analysis of the fold difference of hormone receptor protein levels relative to control untreated cells indicated in the histogram ( n = 3–4). MDA-MB-134 VI ( C ) and SUM44-PE ( D ) invasive lobular breast carcinoma cells were treated with the indicated concentrations of PQ for 24 h prior to lysis and immunoblotting. Histograms indicate the fold change in ER-α protein levels relative to untreated cells ( n = 4). E MCF-7 cells were treated with the indicated concentrations of PQ and MON for 24 h. Lysates were immunoblotted with ER-α and AR antibodies, and the histogram indicates the fold difference in protein levels relative to untreated cells ( n = 3)
Bt474 Cells, supplied by Genolytic 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/product/bt474+cells/pmc06910226-62-5-13?v=Genolytic+GmbH
Average 90 stars, based on 1 article reviews
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Anticancer Inc bt474-gfp cells
Endosomal recycling inhibitors downregulate ER-α and AR. A Heatmap displaying the top 30 hits from the RPPA analysis of control and 10 µM PQ-treated <t>BT474</t> cells (mean of two biological replicates; * indicates AR and ER-α). B Lysates of BT474 cells treated with 10 µM PQ for 24 h were immunoblotted with the indicated antibodies. Quantitative analysis of the fold difference of hormone receptor protein levels relative to control untreated cells indicated in the histogram ( n = 3–4). MDA-MB-134 VI ( C ) and SUM44-PE ( D ) invasive lobular breast carcinoma cells were treated with the indicated concentrations of PQ for 24 h prior to lysis and immunoblotting. Histograms indicate the fold change in ER-α protein levels relative to untreated cells ( n = 4). E MCF-7 cells were treated with the indicated concentrations of PQ and MON for 24 h. Lysates were immunoblotted with ER-α and AR antibodies, and the histogram indicates the fold difference in protein levels relative to untreated cells ( n = 3)
Bt474 Gfp Cells, supplied by Anticancer 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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Image Search Results


Effect of magnetic thermoablation on the BCL2, HSP70, and FGF-R1 protein expression pattern in BT474 tumors. Notes: Representative pictures after IHC staining of BCL2, HSP70, and FGF-R1 were chosen. Blue: nuclei, red: protein-specific antibody, scale bar: 100 μm. Relative semi-quantitative expression of investigated proteins is depicted in diagrams. In diagrams, bars represent the relative number of slides with a specific protein expression normalized to the total number of all slides in the specific treatment group. Bar colors represent the amount of specifically stained area within the viable tumor region: unstained/negative (light gray), less than 50% of vital area stained (dark grey), more than 50% of vital area stained (black). Whereas a downregulation of BCL2 and FGF-R1 can be assumed, HSP70 expression remained unchanged. Abbreviations: BCL2, B-cell lymphoma 2; HSP70, heat shock protein; FGF-R1, fibroblast growth factor receptor 1; IHC, immunohistochemistry; MNP, magnetic nanoparticles; AMF, alternating magnetic field.

Journal: International Journal of Nanomedicine

Article Title: Magnetic thermoablation stimuli alter BCL2 and FGF-R1 but not HSP70 expression profiles in BT474 breast tumors

doi: 10.2147/IJN.S77372

Figure Lengend Snippet: Effect of magnetic thermoablation on the BCL2, HSP70, and FGF-R1 protein expression pattern in BT474 tumors. Notes: Representative pictures after IHC staining of BCL2, HSP70, and FGF-R1 were chosen. Blue: nuclei, red: protein-specific antibody, scale bar: 100 μm. Relative semi-quantitative expression of investigated proteins is depicted in diagrams. In diagrams, bars represent the relative number of slides with a specific protein expression normalized to the total number of all slides in the specific treatment group. Bar colors represent the amount of specifically stained area within the viable tumor region: unstained/negative (light gray), less than 50% of vital area stained (dark grey), more than 50% of vital area stained (black). Whereas a downregulation of BCL2 and FGF-R1 can be assumed, HSP70 expression remained unchanged. Abbreviations: BCL2, B-cell lymphoma 2; HSP70, heat shock protein; FGF-R1, fibroblast growth factor receptor 1; IHC, immunohistochemistry; MNP, magnetic nanoparticles; AMF, alternating magnetic field.

Article Snippet: For tumor implantation, 200 μL Matrigel (BD MatrigelTM Basement Membrane Matrix; Becton Dickinson GmbH, Germany) containing 1×10 7 BT474 cells (human mammary-adenocarcinoma, Cell Lines Service, Germany) were injected subcutaneously between the shoulder blades of 6–15 week old female severe combined immune deficiency (SCID)–Balb/c mice (Harlan Laboratories, the Netherlands).

Techniques: Expressing, Immunohistochemistry, Staining

DOTA-PNA-Peptide Cu-64 radiolabeling and  BT474  Cellular Uptake

Journal: Nuclear medicine and biology

Article Title: Determining Efficacy of Breast Cancer Therapy by PET Imaging of HER2 mRNA

doi: 10.1016/j.nucmedbio.2013.08.005

Figure Lengend Snippet: DOTA-PNA-Peptide Cu-64 radiolabeling and BT474 Cellular Uptake

Article Snippet: Human BT474 BC Xenografts For tumor induction, 5–6 × 10 6 BT474 cells in 0.2 mL of culture medium, including 10 mg of Matrigel (Becton-Dickinson), were implanted intramuscularly through a sterile 27 gauge needle into the thighs of 6–8 week old female NCr immunocompromised mice (National Cancer Institute), lightly anesthetized with a mixture of ketamine (200 mg/kg), xylazine (10 mg/kg) and acetopromazine (2 mg/kg) at a dose of 160 μL/25 g, as before ( 11 ).

Techniques: Radioactivity

Surface rendered F-18-FDG and Cu-64-WT4340 images of a mouse bearing BT474 tumor (arrow) in the right thigh. Images in A and C are before treatment and in B and D are after second Dox treatment. Top: Cu-64-WT4340 (A, B) Bottom: F-18-FDG (C, D). A significantly diminished uptake of Cu-64-WT4340 after Dox treatment is visible in (B) as compared to that with the F-18-FDG uptake (D). Note: significant muscle uptake of F-18-FDG in contralateral normal thigh (C).

Journal: Nuclear medicine and biology

Article Title: Determining Efficacy of Breast Cancer Therapy by PET Imaging of HER2 mRNA

doi: 10.1016/j.nucmedbio.2013.08.005

Figure Lengend Snippet: Surface rendered F-18-FDG and Cu-64-WT4340 images of a mouse bearing BT474 tumor (arrow) in the right thigh. Images in A and C are before treatment and in B and D are after second Dox treatment. Top: Cu-64-WT4340 (A, B) Bottom: F-18-FDG (C, D). A significantly diminished uptake of Cu-64-WT4340 after Dox treatment is visible in (B) as compared to that with the F-18-FDG uptake (D). Note: significant muscle uptake of F-18-FDG in contralateral normal thigh (C).

Article Snippet: Human BT474 BC Xenografts For tumor induction, 5–6 × 10 6 BT474 cells in 0.2 mL of culture medium, including 10 mg of Matrigel (Becton-Dickinson), were implanted intramuscularly through a sterile 27 gauge needle into the thighs of 6–8 week old female NCr immunocompromised mice (National Cancer Institute), lightly anesthetized with a mixture of ketamine (200 mg/kg), xylazine (10 mg/kg) and acetopromazine (2 mg/kg) at a dose of 160 μL/25 g, as before ( 11 ).

Techniques:

Percent of Pretreatment Tumor Volume (TV) and Body Weight (BW) of mice bearing  BT474  Xenografts with and without (n=8) Doxorubicin Treatment (n=8)

Journal: Nuclear medicine and biology

Article Title: Determining Efficacy of Breast Cancer Therapy by PET Imaging of HER2 mRNA

doi: 10.1016/j.nucmedbio.2013.08.005

Figure Lengend Snippet: Percent of Pretreatment Tumor Volume (TV) and Body Weight (BW) of mice bearing BT474 Xenografts with and without (n=8) Doxorubicin Treatment (n=8)

Article Snippet: Human BT474 BC Xenografts For tumor induction, 5–6 × 10 6 BT474 cells in 0.2 mL of culture medium, including 10 mg of Matrigel (Becton-Dickinson), were implanted intramuscularly through a sterile 27 gauge needle into the thighs of 6–8 week old female NCr immunocompromised mice (National Cancer Institute), lightly anesthetized with a mixture of ketamine (200 mg/kg), xylazine (10 mg/kg) and acetopromazine (2 mg/kg) at a dose of 160 μL/25 g, as before ( 11 ).

Techniques: Control

Endosomal recycling inhibitors downregulate ER-α and AR. A Heatmap displaying the top 30 hits from the RPPA analysis of control and 10 µM PQ-treated BT474 cells (mean of two biological replicates; * indicates AR and ER-α). B Lysates of BT474 cells treated with 10 µM PQ for 24 h were immunoblotted with the indicated antibodies. Quantitative analysis of the fold difference of hormone receptor protein levels relative to control untreated cells indicated in the histogram ( n = 3–4). MDA-MB-134 VI ( C ) and SUM44-PE ( D ) invasive lobular breast carcinoma cells were treated with the indicated concentrations of PQ for 24 h prior to lysis and immunoblotting. Histograms indicate the fold change in ER-α protein levels relative to untreated cells ( n = 4). E MCF-7 cells were treated with the indicated concentrations of PQ and MON for 24 h. Lysates were immunoblotted with ER-α and AR antibodies, and the histogram indicates the fold difference in protein levels relative to untreated cells ( n = 3)

Journal: Breast Cancer Research and Treatment

Article Title: Endosomal recycling inhibitors downregulate estrogen receptor-alpha and synergise with endocrine therapies

doi: 10.1007/s10549-023-07225-2

Figure Lengend Snippet: Endosomal recycling inhibitors downregulate ER-α and AR. A Heatmap displaying the top 30 hits from the RPPA analysis of control and 10 µM PQ-treated BT474 cells (mean of two biological replicates; * indicates AR and ER-α). B Lysates of BT474 cells treated with 10 µM PQ for 24 h were immunoblotted with the indicated antibodies. Quantitative analysis of the fold difference of hormone receptor protein levels relative to control untreated cells indicated in the histogram ( n = 3–4). MDA-MB-134 VI ( C ) and SUM44-PE ( D ) invasive lobular breast carcinoma cells were treated with the indicated concentrations of PQ for 24 h prior to lysis and immunoblotting. Histograms indicate the fold change in ER-α protein levels relative to untreated cells ( n = 4). E MCF-7 cells were treated with the indicated concentrations of PQ and MON for 24 h. Lysates were immunoblotted with ER-α and AR antibodies, and the histogram indicates the fold difference in protein levels relative to untreated cells ( n = 3)

Article Snippet: Authenticated BT474 cells were purchased from CalTag Medsystems and cultured in DMEM.

Techniques: Lysis, Western Blot