MAB1663 Search Results


94
Bio-Techne corporation human mouse rat hsp70 hspa1a antibody
Human Mouse Rat Hsp70 Hspa1a Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/MAB1663/pm38088826-51-5-16?v=Bio-Techne+corporation
Average 94 stars, based on 1 article reviews
human mouse rat hsp70 hspa1a antibody - by Bioz Stars, 2026-07
94/100 stars
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92
R&D Systems mo anti human rd systems mab1663
List of the 20 proteins quantified using the Reverse Phase Protein Array (RPPA) technique. The suppliers and conditions for each primary antibody used in this study after western blotting validation are given.
Mo Anti Human Rd Systems Mab1663, supplied by R&D Systems, 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/MAB1663/pmc05994332-13-7-9?v=R%26D+Systems
Average 92 stars, based on 1 article reviews
mo anti human rd systems mab1663 - by Bioz Stars, 2026-07
92/100 stars
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99
R&D Systems hsp70
T-PNU displays immunogenic cell death properties. a , EMT6-hHER2 cell death kinetics induced by T-PNU. Percentage of early (annexin V + /DAPI − ) and late (annexin V + /DAPI + ) apoptotic cells and necrotic cells (annexin V − /DAPI + ) was determined by flow cytometry. Data presented as mean ± SD for 3 independent experiments. b , Representative dot plots of flow cytometry analysis of cell death induced by T-PNU, idarubicine and UVB radiation at indicated time points. c , T-PNU induction of <t>HSP70,</t> HSP90 and CRT on EMT6-hHER2 cells. UVB treated cells are used as controls. Experiments were performed in triplicates. d , Representative immunofluorescence staining of HSP70, HSP90 and CRT on EMT6-hHER2 following T-PNU treatment. The presence of indicated markers on the cell surface was verified by confocal microscopy. e , T-PNU induces oxidative stress and production of reactive oxygen species (ROS). ROS were stained by CellRox Deep Red reagent and detected by flow cytometry. Experiments were performed in triplicates. f , Quantification of intracellular or extracellular ATP levels in EMT6-hHER2 cell line exposed to T-PNU, idarubicine and UVB. Data presented as mean ± SD for 3 independent experiments. g , HMGB1 release into EMT6-hHER2 culture supernatants induced by T-PNU. The compiled results of a total of 3 experiments are shown
Hsp70, supplied by R&D Systems, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/MAB1663/pmc06341578-43-0-1?v=R%26D+Systems
Average 99 stars, based on 1 article reviews
hsp70 - by Bioz Stars, 2026-07
99/100 stars
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Image Search Results


List of the 20 proteins quantified using the Reverse Phase Protein Array (RPPA) technique. The suppliers and conditions for each primary antibody used in this study after western blotting validation are given.

Journal: PeerJ

Article Title: Beef tenderness and intramuscular fat proteomic biomarkers: muscle type effect

doi: 10.7717/peerj.4891

Figure Lengend Snippet: List of the 20 proteins quantified using the Reverse Phase Protein Array (RPPA) technique. The suppliers and conditions for each primary antibody used in this study after western blotting validation are given.

Article Snippet: Hsp70-1A ( HSPA1A ) , Q27975 , Mo. anti-human RD Systems MAB1663 , 1/1000.

Techniques: Protein Array, Western Blot, Biomarker Discovery, Protein Binding

T-PNU displays immunogenic cell death properties. a , EMT6-hHER2 cell death kinetics induced by T-PNU. Percentage of early (annexin V + /DAPI − ) and late (annexin V + /DAPI + ) apoptotic cells and necrotic cells (annexin V − /DAPI + ) was determined by flow cytometry. Data presented as mean ± SD for 3 independent experiments. b , Representative dot plots of flow cytometry analysis of cell death induced by T-PNU, idarubicine and UVB radiation at indicated time points. c , T-PNU induction of HSP70, HSP90 and CRT on EMT6-hHER2 cells. UVB treated cells are used as controls. Experiments were performed in triplicates. d , Representative immunofluorescence staining of HSP70, HSP90 and CRT on EMT6-hHER2 following T-PNU treatment. The presence of indicated markers on the cell surface was verified by confocal microscopy. e , T-PNU induces oxidative stress and production of reactive oxygen species (ROS). ROS were stained by CellRox Deep Red reagent and detected by flow cytometry. Experiments were performed in triplicates. f , Quantification of intracellular or extracellular ATP levels in EMT6-hHER2 cell line exposed to T-PNU, idarubicine and UVB. Data presented as mean ± SD for 3 independent experiments. g , HMGB1 release into EMT6-hHER2 culture supernatants induced by T-PNU. The compiled results of a total of 3 experiments are shown

Journal: Journal for Immunotherapy of Cancer

Article Title: A novel anti-HER2 anthracycline-based antibody-drug conjugate induces adaptive anti-tumor immunity and potentiates PD-1 blockade in breast cancer

doi: 10.1186/s40425-018-0464-1

Figure Lengend Snippet: T-PNU displays immunogenic cell death properties. a , EMT6-hHER2 cell death kinetics induced by T-PNU. Percentage of early (annexin V + /DAPI − ) and late (annexin V + /DAPI + ) apoptotic cells and necrotic cells (annexin V − /DAPI + ) was determined by flow cytometry. Data presented as mean ± SD for 3 independent experiments. b , Representative dot plots of flow cytometry analysis of cell death induced by T-PNU, idarubicine and UVB radiation at indicated time points. c , T-PNU induction of HSP70, HSP90 and CRT on EMT6-hHER2 cells. UVB treated cells are used as controls. Experiments were performed in triplicates. d , Representative immunofluorescence staining of HSP70, HSP90 and CRT on EMT6-hHER2 following T-PNU treatment. The presence of indicated markers on the cell surface was verified by confocal microscopy. e , T-PNU induces oxidative stress and production of reactive oxygen species (ROS). ROS were stained by CellRox Deep Red reagent and detected by flow cytometry. Experiments were performed in triplicates. f , Quantification of intracellular or extracellular ATP levels in EMT6-hHER2 cell line exposed to T-PNU, idarubicine and UVB. Data presented as mean ± SD for 3 independent experiments. g , HMGB1 release into EMT6-hHER2 culture supernatants induced by T-PNU. The compiled results of a total of 3 experiments are shown

Article Snippet: HSP70 (R&D Systems, #RD-MAB1663), HSP90 (Enzo Life Sciences, #ADI-SPA-830-F) and CRT antibody (Abcam, #ab2907) were used for flow cytometry.

Techniques: Flow Cytometry, Immunofluorescence, Staining, Confocal Microscopy