Cell Migration/Chemotaxis Assay Kit (96-well, 3 µm) (ab235692) uses a Boyden chamber, where the cells migrate through a semi-permeable membrane under different stimuli.
Individual kit components also available for purchase with a minimum order of 20 units. Contact us to discuss your needs.
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- Cells 11:2022The Therapeutic Effect of Phosphopeptide P140 Attenuates Inflammation Induced by Uric Acid Crystals in Gout Arthritis Mouse Model.Applications:Unspecified applicationReactive species:Unspecified reactive speciesIzabela Galvão,Dylan Mastrippolito,Laura Talamini,Mariana Aganetti,Victor Rocha,Cindy Verdot,Viviani Mendes,Vivian Louise Soares de Oliveira,Amanda Dias Braga,Vinicius Dantas Martins,Ana Maria Caetano de Faria,Flávio A Amaral,Philippe Georgel,Angélica T Vieira,Sylviane MullerPubMed 36496970
- Immunity 55:1645-1662.e72022Keratinocyte-derived defensins activate neutrophil-specific receptors Mrgpra2a/b to prevent skin dysbiosis and bacterial infection.Applications:Unspecified applicationReactive species:Unspecified reactive speciesXintong Dong,Nathachit Limjunyawong,Elizabeth I Sypek,Gaofeng Wang,Roger V Ortines,Christine Youn,Martin P Alphonse,Dustin Dikeman,Yu Wang,Mark Lay,Ruchita Kothari,Chirag Vasavda,Priyanka Pundir,Loyal Goff,Lloyd S Miller,Wuyuan Lu,Luis A Garza,Brian S Kim,Nathan K Archer,Xinzhong DongPubMed 35882236
- Cancer immunology research 9:200-2132020Targeted Deletion of CXCR2 in Myeloid Cells Alters the Tumor Immune Environment to Improve Antitumor Immunity.Applications:Unspecified applicationReactive species:Unspecified reactive speciesJinming Yang,Chi Yan,Anna E Vilgelm,Sheau-Chiann Chen,Gregory D Ayers,Christopher A Johnson,Ann RichmondPubMed 33177110
Key facts
- Detection method
Fluorescent
- Sample types
Suspension cells, Adherent cells
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Cell Migration/Chemotaxis Assay Kit (96-well, 3 µm) (ab235692) uses a Boyden chamber, where the cells migrate through a semi-permeable membrane under different stimuli.
Individual kit components also available for purchase with a minimum order of 20 units. Contact us to discuss your needs.
Key facts
- Detection method
Fluorescent
- Sample types
Suspension cells, Adherent cells
- Assay Platform
Microplate reader
Storage
- Shipped at conditions
Blue Ice
- Appropriate short-term storage conditions
-20°C
- Appropriate long-term storage conditions
-20°C
- Storage information
-20°C
Notes
Cell Migration/Chemotaxis Assay Kit (96-well, 3 μm) (ab235692) utilizes a Boyden chamber, where the cells migrate through a semi-permeable membrane under different stimuli. Cell migration can be analyzed directly by reading fluorescence (Ex/Em = 530/590 nm) in a plate reader. Our assay is easy to use, sensitive and adaptable to high-throughput systems.
This product is manufactured by BioVision, an Abcam company and was previously called K908 EZCellTM Cell Migration/Chemotaxis Assay Kit (96-well, 3 μm). K908-100 is the same size as the 100 test size of ab235692.
Cell invasion is the ability of cells to migrate from one area to another through an extracellular matrix. Cell invasion is exhibited by both normal cells as well as cancerous cells in response to specific external signals, including chemical and mechanical stimuli. During invasion, extracellular matrix is enzymatically degraded by cellular proteases before cells migrate to the new location. Cell invasion is required for normal processes such as wound repair, vasculature formation and the inflammatory response as well as the abnormal invasion of tissues by tumor cells during metastasis.
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2 product images
Functional Studies - Cell Migration/Chemotaxis Assay Kit (96-well, 3 µm) (ab235692)
Standard Curve.
Erythroleukemia cells were harvested, counted and serially diluted to obtain desired cell number. Cells were incubated according to the protocol.
Functional Studies - Cell Migration/Chemotaxis Assay Kit (96-well, 3 µm) (ab235692)
Cell Invasion.
Erythroleukemia cells were starved overnight and treated with Control (Cnt) Invasion Inducer or remain untreated (Untreated cells). Treatment with Control Invasion Inducer demonstrated a significant increase in invasion as compared to untreated control cells.
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