Flow Cell Priming

Flow cell priming is the preparatory process of conditioning a flow cell before a biochemical assay or nanopore sequencing run, helping establish the fluidic and chemical environment required for reliable measurements. The procedure introduces a priming solution through the flow cell to replace storage solution, remove trapped air, equilibrate the membrane, and establish appropriate ionic conditions across active channels. Proper priming supports consistent sample loading and signal generation, while incomplete priming can reduce channel availability or introduce measurement variability. In biochemistry, this step improves experimental reproducibility and helps researchers obtain higher-quality data from membrane-based analytical platforms.

Flow Cell Priming - Related Videos

Research

JoVE Journal - Immunology and Infection

Tractable Mammalian Cell Infections with Protozoan-primed Bacteria

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Cited by 2 •

2013

This technique provides a method to harvest, normalize and quantify intracellular growth of bacterial pathogens that are pre-cultivated in natural protozoan host cells prior to infections of mammalian cells. This method can be modified to accommodate a wide variety of host cells for the priming stage as well as target cell types.

Education

JoVE Science Education - Psychology
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Verbal Priming

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2023

Source: Laboratory of Jonathan Flombaum—Johns Hopkins University Human memory seems to work in two broad ways. Like modern computers, the human mind has explicit, or declarative, memory: ask a question, and a person gives the best answer they can. Input a query, and a computer program returns the contents of the relevant parts of its stored memory. Humans also have a second kind of memory system, one not really typical of computers, one that experimental psychologists call implicit. Implicit...

Flow Cytometry Purification of Mouse Meiotic Cells

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Cited by 65 •

2011

An efficient method to obtain highly purified viable meiotic fractions from mouse testis is described, which combines a refined cell dissociation protocol with fluorescent activated cell sorting (FACS). This method takes advantage of differences in the DNA content and nuclear density of discrete meiotic fractions.

Intravital Imaging of Neutrophil Priming Using IL-1β Promoter-driven DsRed Reporter Mice

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Cited by 1 •

2016

This current protocol employs fluorescent reporters, in vivo labeling, and intravital imaging techniques to enable monitoring of the dynamic process of neutrophil priming in living animals.

Research

JoVE Journal - Biology
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Platelet Adhesion and Aggregation Under Flow using Microfluidic Flow Cells

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Cited by 29 •

2009

The platelet adhesion cascade takes place in the presence of shear flow, a factor not accounted for in conventional (static) well-plate assays. This article reports on a platelet-aggregation assay utilizing a microfluidic well-plate format to emulate physiological shear flow conditions.

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