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Output Catalog

ASAP is committed to accelerating the pace of discovery and informing a path to a cure for Parkinson’s disease through collaboration, research-enabling resources, and data sharing. We’ve created this catalog to showcase the research outputs and tools developed by ASAP-funded programs.

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GRIN lens implant (1 mm) Protocol

This is the standard 1 mm GRIN lens implant protocol for Rodrigues-Vaz and Athalye et al, 2025.

Program: Collaborative Research Network
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EMG recordings-Rodrigues-Vaz and Athalye et al, 2025

This is the standard protocol for recordings of bulk EMG used for Rodrigues-Vaz and Athalye et al, 2025.

Program: Collaborative Research Network
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Perfusion and Histology Rodrigues-Vaz and Athalye et al, 2025

This is the standard protocol for perfusion and histology of brain slices for Rodrigues-Vaz and Athalye et al, 2025.

Program: Collaborative Research Network
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Isometric forelimb task behavioral training

This task is a self-paced task in which mice are reinforced for using their forelimb to apply force to an immobile joystick exceeding a threshold of duration and force.

Program: Collaborative Research Network
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Holographic calibration

This is the standard protocol for 2-photon holographic calibration with In vivo Ultima Bruker microscope through GRIN lens used for Rodrigues-Vaz and Athalye et al, 2025.

Program: Collaborative Research Network
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Imaging using 2-photon microscope through GRIN lens

This is the standard protocol for 2-photon imaging with Bruker microscope through GRIN lens used for Rodrigues-Vaz and Athalye et al, 2025.

Program: Collaborative Research Network
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Immunoprecipitation of NAP1-GFP

This protocol describes the procedure to perform immunoprecipitation of NAP1-GFP from HAP1 cells.

Program: Collaborative Research Network
Team:
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Plasmid Construction and Gibson cloning

This protocol describes plasmid construction using Gibson cloning.

Program: Collaborative Research Network
Team:
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Histology Albarran et al 2025

Histology protocol for Albarran et al 2025 that was adapted from Fushiki et al 2024 , to quantify Th+ cells.

Program: Collaborative Research Network
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Cryo-electron tomography of thinned synapses

Protocol for cryo-ET of thinned synapses in rat neuron cultures is detailed. Cryo-FIB milling creates thin samples for high-resolution imaging. Synapse targeting with and without cryo-FLM correlation is explained.

Program: Collaborative Research Network
Team:
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Single particle analysis of α-Synuclein fibrils

Aggregates of α-Synuclein are linked to Parkinson’s, multiple system atrophy, and Lewy body dementia. This protocol outlines near-atomic resolution structures of these amyloid fibrils using cryo-EM single particle analysis.

Program: Collaborative Research Network
Team:
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Preparing primary sandwich hippocampal neuron cultures for cryo-electron tomography

Sandwich hippocampal neuron cultures have low cell density and few glial cells, making them ideal for targeting neurons for cryo-electron tomography.

Program: Collaborative Research Network
Team:
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Sample Preparation Correlative XPCT – Histology

This protocol describes the placement of samples for XPCT and preparation of correlative histological analysis after the measurement.

Program: Collaborative Research Network
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Protocols Suite — SH-SY5Y / iCell® Neurons / High-Content Imaging

Maintenance of SH-SY5Y cells with SNCA overexpression in DMEM/F-12, differentiation with RA/BDNF, and culture of iCell DopaNeurons with SNCA mutation. Treatment and immunostaining for downstream assays using specific protocols and analysis tools.

Program: Collaborative Research Network
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GCase activity assay

Protocol measures GCase activity using 4-MUG substrate. GCase protein from a cellular model is diluted in acidic buffer to mimic lysosome pH. Adding lipid/detergent maintains enzyme activity. Taurocholate bile salt is included in the protocol.

Program: Collaborative Research Network
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