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Fisher Scientific diff-quick staining solution
Diff Quick Staining Solution, supplied by Fisher Scientific, 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/diff-quick+staining+solution/diff+quick+stain+set/pmc09655042-209-36-39
Average 90 stars, based on 1 article reviews
diff-quick staining solution - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Staining:

Article Title: Pulmonary Toxicity and Proteomic Analysis in Bronchoalveolar Lavage Fluids and Lungs of Rats Exposed to Copper Oxide Nanoparticles
Article Snippet: The total number of cells in the BALF were counted with a Vi-Cell ® XR analyzer (Beckman Coulter, Brea, CA, USA), and cell differential tests were performed using cytospin preparations (Shandon, Pittsburgh, PA, USA) stained with Diff-Quick staining solution (Fisher Scientific, Swedesboro, NJ, USA).

Article Title: Agents and use thereof
Article Snippet: The chambers are incubated in the cell incubator for 6 h to 24 h. The transwells are stained (Diff-Quick staining solution, Fisher Scientific) and, after scraping off the noninvaded cells with a cotton swab, the invaded cells are counted in a light microscope.

Article Title: Evidence of gamma-tocotrienol as an apoptosis-inducing, invasion-suppressing, and chemotherapy drug-sensitizing agent in human melanoma cells.
Article Snippet: Evidence of γ-Tocotrienol as an Apoptosis-Inducing, Invasion-Suppressing, and Chemotherapy DrugSensitizing Agent in Human Melanoma Cells Piek Ngoh Chang a , Wei Ney Yap a , Davy Tak Wing Lee b , M. T. Ling b , Y. C. Wong b & Yee Leng Yap a a Davos Life Science Pte.. Ltd., Cancer Research Laboratory , Singapore b Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine , The University of Hong Kong , Hong Kong, SAR Published online: 16 Apr 2009.

Article Title: Id1, inhibitor of differentiation, is a key protein mediating anti-tumor responses of gamma-tocotrienol in breast cancer cells.
Article Snippet: a Davos Life Science Pte.. Ltd., Cancer Research Laboratory, 16 Tuas South Street 5, Singapore b Singapore Bioimaging Consortium (SBIC), Biomedical Sciences Institutes, 11 Biopolis Way #02-02 Helios, Singapore 138667, Singapore c Duke-NUS Graduate Medical School Singapore, 8 College Road, Singapore 169857, Singapore d College of Light Industry and Food Sciences, South China University of Technology, Guang Zhou, China e Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 1/F, Laboratory Block, 21 Sassoon Road, Hong Kong SAR, China f Australian Prostate Cancer Research Centre-Queensland Institute of Health and Biomedical Innovation (IHBI), QUT, Australia

Diff-Quik:

Article Title: Pulmonary Toxicity and Proteomic Analysis in Bronchoalveolar Lavage Fluids and Lungs of Rats Exposed to Copper Oxide Nanoparticles
Article Snippet: The total number of cells in the BALF were counted with a Vi-Cell ® XR analyzer (Beckman Coulter, Brea, CA, USA), and cell differential tests were performed using cytospin preparations (Shandon, Pittsburgh, PA, USA) stained with Diff-Quick staining solution (Fisher Scientific, Swedesboro, NJ, USA).

Article Title: Agents and use thereof
Article Snippet: The chambers are incubated in the cell incubator for 6 h to 24 h. The transwells are stained (Diff-Quick staining solution, Fisher Scientific) and, after scraping off the noninvaded cells with a cotton swab, the invaded cells are counted in a light microscope.

Article Title: Evidence of gamma-tocotrienol as an apoptosis-inducing, invasion-suppressing, and chemotherapy drug-sensitizing agent in human melanoma cells.
Article Snippet: Evidence of γ-Tocotrienol as an Apoptosis-Inducing, Invasion-Suppressing, and Chemotherapy DrugSensitizing Agent in Human Melanoma Cells Piek Ngoh Chang a , Wei Ney Yap a , Davy Tak Wing Lee b , M. T. Ling b , Y. C. Wong b & Yee Leng Yap a a Davos Life Science Pte.. Ltd., Cancer Research Laboratory , Singapore b Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine , The University of Hong Kong , Hong Kong, SAR Published online: 16 Apr 2009.

Article Title: Id1, inhibitor of differentiation, is a key protein mediating anti-tumor responses of gamma-tocotrienol in breast cancer cells.
Article Snippet: a Davos Life Science Pte.. Ltd., Cancer Research Laboratory, 16 Tuas South Street 5, Singapore b Singapore Bioimaging Consortium (SBIC), Biomedical Sciences Institutes, 11 Biopolis Way #02-02 Helios, Singapore 138667, Singapore c Duke-NUS Graduate Medical School Singapore, 8 College Road, Singapore 169857, Singapore d College of Light Industry and Food Sciences, South China University of Technology, Guang Zhou, China e Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 1/F, Laboratory Block, 21 Sassoon Road, Hong Kong SAR, China f Australian Prostate Cancer Research Centre-Queensland Institute of Health and Biomedical Innovation (IHBI), QUT, Australia

Incubation:

Article Title: Pulmonary Toxicity and Proteomic Analysis in Bronchoalveolar Lavage Fluids and Lungs of Rats Exposed to Copper Oxide Nanoparticles
Article Snippet: The total number of cells in the BALF were counted with a Vi-Cell ® XR analyzer (Beckman Coulter, Brea, CA, USA), and cell differential tests were performed using cytospin preparations (Shandon, Pittsburgh, PA, USA) stained with Diff-Quick staining solution (Fisher Scientific, Swedesboro, NJ, USA).

Article Title: Agents and use thereof
Article Snippet: The chambers are incubated in the cell incubator for 6 h to 24 h. The transwells are stained (Diff-Quick staining solution, Fisher Scientific) and, after scraping off the noninvaded cells with a cotton swab, the invaded cells are counted in a light microscope.

Article Title: Evidence of gamma-tocotrienol as an apoptosis-inducing, invasion-suppressing, and chemotherapy drug-sensitizing agent in human melanoma cells.
Article Snippet: Evidence of γ-Tocotrienol as an Apoptosis-Inducing, Invasion-Suppressing, and Chemotherapy DrugSensitizing Agent in Human Melanoma Cells Piek Ngoh Chang a , Wei Ney Yap a , Davy Tak Wing Lee b , M. T. Ling b , Y. C. Wong b & Yee Leng Yap a a Davos Life Science Pte.. Ltd., Cancer Research Laboratory , Singapore b Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine , The University of Hong Kong , Hong Kong, SAR Published online: 16 Apr 2009.

Article Title: Id1, inhibitor of differentiation, is a key protein mediating anti-tumor responses of gamma-tocotrienol in breast cancer cells.
Article Snippet: a Davos Life Science Pte.. Ltd., Cancer Research Laboratory, 16 Tuas South Street 5, Singapore b Singapore Bioimaging Consortium (SBIC), Biomedical Sciences Institutes, 11 Biopolis Way #02-02 Helios, Singapore 138667, Singapore c Duke-NUS Graduate Medical School Singapore, 8 College Road, Singapore 169857, Singapore d College of Light Industry and Food Sciences, South China University of Technology, Guang Zhou, China e Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 1/F, Laboratory Block, 21 Sassoon Road, Hong Kong SAR, China f Australian Prostate Cancer Research Centre-Queensland Institute of Health and Biomedical Innovation (IHBI), QUT, Australia

Light Microscopy:

Article Title: Pulmonary Toxicity and Proteomic Analysis in Bronchoalveolar Lavage Fluids and Lungs of Rats Exposed to Copper Oxide Nanoparticles
Article Snippet: The total number of cells in the BALF were counted with a Vi-Cell ® XR analyzer (Beckman Coulter, Brea, CA, USA), and cell differential tests were performed using cytospin preparations (Shandon, Pittsburgh, PA, USA) stained with Diff-Quick staining solution (Fisher Scientific, Swedesboro, NJ, USA).

Article Title: Agents and use thereof
Article Snippet: The chambers are incubated in the cell incubator for 6 h to 24 h. The transwells are stained (Diff-Quick staining solution, Fisher Scientific) and, after scraping off the noninvaded cells with a cotton swab, the invaded cells are counted in a light microscope.

Article Title: Evidence of gamma-tocotrienol as an apoptosis-inducing, invasion-suppressing, and chemotherapy drug-sensitizing agent in human melanoma cells.
Article Snippet: Evidence of γ-Tocotrienol as an Apoptosis-Inducing, Invasion-Suppressing, and Chemotherapy DrugSensitizing Agent in Human Melanoma Cells Piek Ngoh Chang a , Wei Ney Yap a , Davy Tak Wing Lee b , M. T. Ling b , Y. C. Wong b & Yee Leng Yap a a Davos Life Science Pte.. Ltd., Cancer Research Laboratory , Singapore b Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine , The University of Hong Kong , Hong Kong, SAR Published online: 16 Apr 2009.

Article Title: Id1, inhibitor of differentiation, is a key protein mediating anti-tumor responses of gamma-tocotrienol in breast cancer cells.
Article Snippet: a Davos Life Science Pte.. Ltd., Cancer Research Laboratory, 16 Tuas South Street 5, Singapore b Singapore Bioimaging Consortium (SBIC), Biomedical Sciences Institutes, 11 Biopolis Way #02-02 Helios, Singapore 138667, Singapore c Duke-NUS Graduate Medical School Singapore, 8 College Road, Singapore 169857, Singapore d College of Light Industry and Food Sciences, South China University of Technology, Guang Zhou, China e Department of Anatomy, Cancer Biology Lab, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 1/F, Laboratory Block, 21 Sassoon Road, Hong Kong SAR, China f Australian Prostate Cancer Research Centre-Queensland Institute of Health and Biomedical Innovation (IHBI), QUT, Australia



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Effect of IL-13Rα2 on migration and invasion activity of osteosarcoma cells: ( A ) Migration assay was conducted by seeding 1 × 10 5 cells into the upper chamber of each well. ( B ) Invasion assays were performed by seeding 2 × 10 5 cells in each well of the Matrigel-coated upper chamber. Serum-free media was used in the upper chamber for both migration and invasion assays, while the lower chamber contained media with 10% serum to serve as a chemoattractant. The migrated or invaded cells were <t>stained</t> with <t>Diff</t> <t>Quick</t> staining <t>solution</t> and counted in five separate ×100 microscopic fields per well. Original magnification, ×400. *** p < 0.001; EV, empty vector for wild-type IL-13Rα2; IL-13Rα2-OE, vector for wild-type IL-13Rα2; shControl, control vector for shRNA; shIL-13Rα2, vector for shRNA for IL-13Rα2.
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https://www.bioz.com/product/diff-quick+staining+solution/diff+quick+stain+set/pmc09655042-209-36-39
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Effect of IL-13Rα2 on migration and invasion activity of osteosarcoma cells: ( A ) Migration assay was conducted by seeding 1 × 10 5 cells into the upper chamber of each well. ( B ) Invasion assays were performed by seeding 2 × 10 5 cells in each well of the Matrigel-coated upper chamber. Serum-free media was used in the upper chamber for both migration and invasion assays, while the lower chamber contained media with 10% serum to serve as a chemoattractant. The migrated or invaded cells were <t>stained</t> with <t>Diff</t> <t>Quick</t> staining <t>solution</t> and counted in five separate ×100 microscopic fields per well. Original magnification, ×400. *** p < 0.001; EV, empty vector for wild-type IL-13Rα2; IL-13Rα2-OE, vector for wild-type IL-13Rα2; shControl, control vector for shRNA; shIL-13Rα2, vector for shRNA for IL-13Rα2.
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Effect of IL-13Rα2 on migration and invasion activity of osteosarcoma cells: ( A ) Migration assay was conducted by seeding 1 × 10 5 cells into the upper chamber of each well. ( B ) Invasion assays were performed by seeding 2 × 10 5 cells in each well of the Matrigel-coated upper chamber. Serum-free media was used in the upper chamber for both migration and invasion assays, while the lower chamber contained media with 10% serum to serve as a chemoattractant. The migrated or invaded cells were <t>stained</t> with <t>Diff</t> <t>Quick</t> staining <t>solution</t> and counted in five separate ×100 microscopic fields per well. Original magnification, ×400. *** p < 0.001; EV, empty vector for wild-type IL-13Rα2; IL-13Rα2-OE, vector for wild-type IL-13Rα2; shControl, control vector for shRNA; shIL-13Rα2, vector for shRNA for IL-13Rα2.
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Average 90 stars, based on 1 article reviews
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Image Search Results


Effect of IL-13Rα2 on migration and invasion activity of osteosarcoma cells: ( A ) Migration assay was conducted by seeding 1 × 10 5 cells into the upper chamber of each well. ( B ) Invasion assays were performed by seeding 2 × 10 5 cells in each well of the Matrigel-coated upper chamber. Serum-free media was used in the upper chamber for both migration and invasion assays, while the lower chamber contained media with 10% serum to serve as a chemoattractant. The migrated or invaded cells were stained with Diff Quick staining solution and counted in five separate ×100 microscopic fields per well. Original magnification, ×400. *** p < 0.001; EV, empty vector for wild-type IL-13Rα2; IL-13Rα2-OE, vector for wild-type IL-13Rα2; shControl, control vector for shRNA; shIL-13Rα2, vector for shRNA for IL-13Rα2.

Journal: Pharmaceuticals

Article Title: IL-13Rα2 Is Involved in Resistance to Doxorubicin and Survival of Osteosarcoma Patients

doi: 10.3390/ph17111526

Figure Lengend Snippet: Effect of IL-13Rα2 on migration and invasion activity of osteosarcoma cells: ( A ) Migration assay was conducted by seeding 1 × 10 5 cells into the upper chamber of each well. ( B ) Invasion assays were performed by seeding 2 × 10 5 cells in each well of the Matrigel-coated upper chamber. Serum-free media was used in the upper chamber for both migration and invasion assays, while the lower chamber contained media with 10% serum to serve as a chemoattractant. The migrated or invaded cells were stained with Diff Quick staining solution and counted in five separate ×100 microscopic fields per well. Original magnification, ×400. *** p < 0.001; EV, empty vector for wild-type IL-13Rα2; IL-13Rα2-OE, vector for wild-type IL-13Rα2; shControl, control vector for shRNA; shIL-13Rα2, vector for shRNA for IL-13Rα2.

Article Snippet: Cells that migrated or invaded to the lower side of the membrane were stained with Diff Quick stain solution (#468.037.1A, Diff-Quick, Dade Behring Inc., Newark, DE, USA).

Techniques: Migration, Activity Assay, Staining, Diff-Quik, Plasmid Preparation, Control, shRNA