Craft Cutter

A craft cutter is a computer-controlled fabrication tool that cuts shapes, patterns, or lettering from thin sheet materials, making it useful for rapid, low-cost prototyping. It works by converting a digital design into tool paths, then moving a blade across the material while controlling direction, speed, and cutting depth to follow the pattern. In bioengineering, this approach can produce stencils, masks, flexible components, and assembly aids for benchtop experiments and device development. Its accessibility and fast turnaround help researchers iterate designs, test geometries, and prepare structured materials without specialized machining equipment.

Craft Cutter - Related Videos

Education

JoVE Core - Organic Chemistry

Limitations of Friedel–Crafts Reactions

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2025

Several restrictions limit the use of Friedel–Crafts reactions. First, the halogen in the alkyl halide must be attached to an sp3-hybridized carbon for the Friedel–Crafts reactions to occur. Vinyl or aryl halides do not react since the carbocations formed are unstable under the reaction conditions. Second, Friedel–Crafts alkylation is susceptible to carbocation rearrangement, and the major products obtained have a rearranged carbon skeleton. In contrast, the acylium ion is stabilized by...

Electrophilic Aromatic Substitution: Friedel–Crafts Alkylation of Benzene

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2023

Friedel–Crafts reactions were developed in 1877 by the French chemist Charles Friedel and the American chemist James Crafts. Friedel–Crafts alkylation refers to the replacement of an aromatic proton with an alkyl group via electrophilic aromatic substitution. A Lewis acid catalyst such as aluminum chloride reacts with an alkyl halide to form a carbocation. The resulting carbocation then reacts with the aromatic ring and undergoes a series of electron rearrangements before giving the final...

Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene

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2025

The Friedel–Crafts acylation reactions involve the addition of an acyl group to an aromatic ring. These reactions proceed via electrophilic aromatic substitution by employing an acyl chloride and a Lewis acid catalyst such as aluminum chloride to form aryl ketone. The mechanism involves the formation of a complex between the Lewis acid and the acyl chloride. An acylium ion is formed by the cleavage of the carbon-chlorine bond of the complex. The acylium ion has a positive charge on the carbon...

Research

JoVE Journal - Engineering
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Adapting Taylor Dispersion to Measure the Dispersion Coefficient of Electrolyte Solutions via an Accessible Microfluidic Setup

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2025

Here, we present a protocol to adapt the Taylor dispersion experiment to the microscale using microchannels fabricated in-house with a desktop craft cutter. The experimental platform can be used to compute the diffusion coefficient of single-species passive tracers and to visualize multispecies ion interaction and separation.

An Integrated Method for Crafting Flexible and Convenient Electrophysiological Optrodes for Multi-Region In Vivo Recording

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2024

We have developed a simplified and cost-effective approach for electrode fabrication and conducted recordings of signals across multiple regions in freely moving mice. Utilizing optogenetics, alongside multi-region electrophysiology and calcium signal recording, enabled the revelation of neuronal activities across regions in the seizure kindling model.

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