3 µm Chemotaxis Assays, 96-Well Format

3 µm Chemotaxis Assays, 96-Well Format
  • Fully quantify chemotaxis with no manual cell counting
  • Measure chemotaxis in less than 6 hours with most cell types
  • Membrane inserts are uncoated to allow use with any chemoattractant
  • Detection with fluorescence plate reader

 

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General FAQs about Chemotaxis Assays

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CytoSelect™ 96-Well Cell Migration Assay, 3 µm
Catalog Number
CBA-104
Size
96 assays
Detection
Fluorometric
Manual/Data Sheet Download
SDS Download
Price
$610.00
CytoSelect™ 96-Well Cell Migration Assay, 3 µm
Catalog Number
CBA-104-5
Size
5 x 96 assays
Detection
Fluorometric
Manual/Data Sheet Download
SDS Download
Price
$2,665.00
Product Details

Chemotaxis describes the movement of cells toward or away from a chemical stimulus in their enviroment. Cell chemotaxis plays a pivotal role in the progression of cancer and other diseases.

CytoSelect™ Cell Migration Assays are ideal for determining the chemotactic properties of cells. The 3 µm pore size is best for the smallest cells including neutrophils and other leukocytes.

CytoSelect™ Chemotaxis Assay Principle. Migratory cells move through the polycarbonate membrane toward a chemoattractant underneath the membrane inserts.

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  1. Irawan, A. et al. (2023). Feeding spent hemp biomass to lactating dairy cows: effects on performance, milk components and quality, blood parameters, and nitrogen metabolism. J Dairy Sci. doi: 10.3168/jds.2023-23829.
  2. Kono, M. et al. (2022). Leaf extracts from Camellia sinensis and Argania spinosa suppress oxidative stress and chemokine release in human 3-dimensional cultured epidermis exposed to PM2.5 collected with cyclonic separation. Fundam Toxicol Sci. 9(4): 117-122. doi: 10.2131/fts.9.117.
  3. Shahbaz, S. et al. (2022). Elevated ATP via enhanced miRNA-30b, 30c, and 30e downregulates the expression of CD73 in CD8+ T cells of HIV-infected individuals. PLoS Pathog. 18(3):e1010378. doi: 10.1371/journal.ppat.1010378.
  4. Jermann, P.M. et al. (2022). Effect of different dietary regimens at dry-off on performance, metabolism, and immune system in dairy cows. J Dairy Sci. doi: 10.3168/jds.2021-21747.
  5. Lajqi, T. et al. (2022). Gut Microbiota-Derived Small Extracellular Vesicles Endorse Memory-like Inflammatory Responses in Murine Neutrophils. Biomedicines. 10(2):442. doi: 10.3390/biomedicines10020442.
  6. Wang, L. et al. (2021). Chromatin Remodeling of Colorectal Cancer Liver Metastasis is Mediated by an HGF-PU.1-DPP4 Axis. Adv Sci (Weinh). doi: 10.1002/advs.202004673.
  7. Jin, X. et al. (2021). Mechanisms of Adiponectin in Regulation of Proinflammatory Cytokine Production and Migration in Macrophages. J Inflamm Res. 14:981-993. doi: 10.2147/JIR.S292137.
  8. Notcovich, S. et al. (2020). Cellular Response of Neutrophils to Bismuth Subnitrate and Micronized Keratin Products In Vitro. Vet Sci. 7(3):E87. doi: 10.3390/vetsci7030087.
  9. Schweitzer, K.S. et al. (2020). IGSF3 mutation identified in patient with severe COPD alters cell function and motility. JCI Insight. doi: 10.1172/jci.insight.138101.
  10. Park, T. et al. (2019). GPR110 (ADGRF1) mediates anti-inflammatory effects of N-docosahexaenoylethanolamine. J Neuroinflammation. 16(1):225. doi: 10.1186/s12974-019-1621-2.
  11. Khoury, O. et al. (2019). Stromal cells from perinatal and adult sources modulate the inflammatory immune response in vitro by decreasing Th1 cell proliferation and cytokine secretion. Stem Cells Transl Med. doi: 10.1002/sctm.19-0123.
  12. Lee, W. et al. (2019). Neutrophils facilitate ovarian cancer premetastatic niche formation in the omentum. J Exp Med. 216(1):176-194. doi: 10.1084/jem.20181170.
  13. Kim, H.K. et al. (2018). A Water-Soluble Extract from Actinidia arguta Ameliorates Psoriasis-Like Skin Inflammation in Mice by Inhibition of Neutrophil Infiltration. Nutrients. 10(10). pii: E1399. doi: 10.3390/nu10101399.
  14. Scully, I.L. et al. (2017). Neutrophil killing of Staphylococcus aureus in diabetes, obesity and metabolic syndrome: a prospective cellular surveillance study. Diabetol Metab Syndr. 9:76. doi: 10.1186/s13098-017-0276-3.
  15. Phan, T.X. et al. (2016). Intrinsic photosensitivity enhances motility of T lymphocytes. Sci. Rep. 6:39479.
  16. Jiang, W. et al. (2016). Infiltration of CCR2+ Ly6Chigh proinflammatory monocytes and neutrophils into the central nervous system is modulated by nicotinic acetylcholine receptors in a model of multiple sclerosis. J Immunol. 196:2095-2108.
  17. Kitano, K. et al. (2014). Rho-kinase activation in leukocytes plays a pivotal role in myocardial ischemia/reperfusion injury. PLoS One.  9:e92242.
  18. Li, X. et al. (2011). Kaposi's Sarcoma-Associated Herpesvirus-Encoded Latency-Associated Nuclear Antigen Reduces Interleukin-8 Expression in Endothelial Cells and Impairs Neutrophil Chemotaxis by Degrading Nuclear p65. J. Virol. 85:8606-8615. 
  19. Chatterjee, S. et al. (2009). Site-Specific Carboxypeptidase B1 Tyrosine Nitration and Pathophysiological Implications following its Physical Association with Nitric Oxide Synthase-3 in Experimental Sepsis. J. Immunol. 183:4055-4066.