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FlowJEM Inc microfluidic drop-seq device
Microfluidic Drop Seq Device, supplied by FlowJEM Inc, 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/drop-seq+microfluidic+device/drop+seq+microfluidic+device/pmc09481908__mmc5-310-17-20
Average 90 stars, based on 1 article reviews
microfluidic drop-seq device - by Bioz Stars, 2026-10
90/100 stars

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Article Title: Single-cell RNA-seq analysis of the brainstem of mutant SOD1 mice reveals perturbed cell types and pathways of amyotrophic lateral sclerosis.
Article Snippet: Briefly, single cell suspensions at 100 cells/μl, EvaGreen droplet generation oil (BIO-RAD, Hercules, CA, USA), and ChemGenes barcoded microparticles (ChemGenes, Wilmington, MA, USA) which contain unique molecular identifiers (UMIs) and cell barcodes were co-flowed through a FlowJEM aquapel-treated Drop-seq microfluidic device (FlowJEM, Toronto, Canada) at recommended flow speeds (oil: 15,000 μl/h, cells: 4000 μl/h, and beads 4000 μl/h) to generate STAMPs.

Article Title: Single-cell RNA-seq analysis of the brainstem of mutant SOD1 mice reveals perturbed cell types and pathways of amyotrophic lateral sclerosis
Article Snippet: Briefly, single cell suspensions at 100 cells/μl, EvaGreen droplet generation oil (BIO-RAD, Hercules, CA, USA), and ChemGenes barcoded microparticles (ChemGenes, Wilmington, MA, USA) which contain unique molecular identifiers (UMIs) and cell barcodes were co-flowed through a FlowJEM aquapel-treated Drop-seq microfluidic device (FlowJEM, Toronto, Canada) at recommended flow speeds (oil: 15,000 μl/h, cells: 4000 μl/h, and beads 4000 μl/h) to generate STAMPS.

Article Title: Single cell molecular alterations reveal target cells and pathways of concussive brain injury.
Article Snippet: The following modifications were made to the online published protocol to obtain enough cDNA as quantified by a high sensitivity BioAnalyzer (Agilent, Santa Clara, CA, USA) to continue the protocol: (1) The number of beads in a single PCR tube was 4000. (2) The number of PCR cycles was 4+ 11 cycles. (3) Multiple PCR tubes were pooled.

Article Title: Systems spatiotemporal dynamics of traumatic brain injury at single cell resolution reveals humanin as a therapeutic target
Article Snippet: Brie y, single cell suspensions at 100 cells/μl, EvaGreen droplet generation oil (Bio-Rad, Hercules, CA, USA), and ChemGenes barcoded Page 16/38 microparticles (ChemGenes, Wilmington, MA, USA) were co- owed through a FlowJEM aquapel-treated Drop-seq micro uidic device (FlowJEM, Toronto, Canada) at recommended ow speeds (oil: 15,000 μl/hr, cells: 4000 μl/hr, and beads 4000 μl/hr) to generate STAMPs.

Article Title: A Tm4sf1 -Marked Subpopulation of Endothelial Stem/Progenitor Cells Identified by Lung Single-Cell Omics of Pulmonary Arterial Hypertension
Article Snippet: Briefly, single cell suspensions at 100 cells/μl, EvaGreen droplet generation oil (BIO-RAD, Hercules, CA, USA), and ChemGenes barcoded microparticles (ChemGenes, Wilmington, MA, USA) were co-flowed through a FlowJEM aquapel-treated Drop-seq microfluidic device (FlowJEM, Toronto, Canada) at recommended flow speeds (oil: 15,000 μl/hr, cells: 4000 μl/hr, and beads 4000 μl/hr) to generate STAMPs.

Article Title: Systems spatiotemporal dynamics of traumatic brain injury at single-cell resolution reveals humanin as a therapeutic target
Article Snippet: Briefly, single-cell suspensions at 100 cells/μl, EvaGreen droplet generation oil (Bio-Rad, Hercules, CA, USA), and ChemGenes barcoded microparticles (ChemGenes, Wilmington, MA, USA) were co-flowed through a FlowJEM aquapel-treated Drop-seq microfluidic device (FlowJEM, Toronto, Canada) at recommended flow speeds (oil: 15,000 μl/h, cells: 4000 μl/h, and beads 4000 μl/h) to generate STAMPs.

Article Title: Diesel Exhaust Particles Dysregulate Multiple Immunological Pathways in Murine Macrophages: Lessons from Microarray and scRNA-seq Technologies
Article Snippet: To generate STAMPs (single-cell transcriptomes attached to microparticles), lung cell samples were run through an aquapel-treated Drop-seq microfluidic device (FlowJEM, Toronto, Canada) where single cells were combined with droplet generation oil (Bio-Rad, Hercules, CA) and barcoded beads (ChemGenes, Wilmington, MA) in lysis buffer into droplets.



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