cat no | io6005
ioGlutamatergic Neurons SNCA A53T/WT are opti‑ox deterministically programmed glutamatergic neurons carrying a genetically engineered heterozygous A53T mutation in the SNCA gene encoding the alpha-synuclein protein. These cells offer a rapidly maturing, consistent and scalable system to study Parkinson's disease (PD).
This disease model is part of a Parkinson's disease panel of physiologically relevant human iPSC-derived cells that can be incorporated into translational research and drug discovery workflows. Additional products in the PD panel include homozygous SNCA A53T, PRKN R275W, PINK1 Q456X and GBA mutations. All disease model cells in the PD panel can be used alongside their genetically matched control, ioGlutamatergic Neurons.
A second SNCA A53T/WT clone is available on enquiry. Studying multiple clones of a specific disease model can lead to a more comprehensive understanding of the impact of the disease-relevant mutation and cellular heterogeneity on associated disease phenotypes.
Confidently investigate your phenotype of interest across multiple clones with our disease model clone panel. Detailed characterisation data (below) and bulk RNA sequencing data (upon request) help you select specific clones if required.
per vial
A maximum number of 20 vials applies. If you would like to order more than 20 vials, please contact us at orders@ÎÞÓǶÌÊÓƵ.
Make True Comparisons
Pair the ioDisease Model Cells with the genetically matched wild-type ioGlutamatergic Neurons to directly investigate the effect of the alpha-synuclein mutation on cellular and molecular mechanisms and cell function.
Scalable
With opti-ox technology, we can make billions of consistently programmed cells, surpassing the demands of industrial workflows.
Quick
The disease model cells and genetically matched control are experiment ready as early as 2 days post revival, and form structural neuronal networks at 10 days.
Schematic overview of the timeline in the user manual
ioGlutamatergic Neurons SNCA A53T/WT are delivered in a cryopreserved format and are programmed to mature rapidly upon revival in the recommended media. The protocol for the generation of these cells is a two-phase process: Phase 1, Stabilisation for 4 days; Phase 2, Maintenance, during which the neurons mature. Phases 1 and 2 after revival of cells are carried out by the customer.
ioGlutamatergic Neurons SNCA A53T/WT express neuron-specific markers comparably to the wild type control
Immunofluorescent staining on day 11 post-revival demonstrates similar homogenous expression of pan-neuronal proteins MAP2 and TUBB3 and glutamatergic neuron-specific transporter VGLUT2 in ioGlutamatergic Neurons SNCA A53T/WT (clone 621P2D1) compared to the genetically matched control. 100X magnification.
ioGlutamatergic Neurons SNCA A53T/WT form structural neuronal networks by day 10
ioGlutamatergic Neurons SNCA A53T/WT (clone 621P2D1) mature rapidly and form structural neuronal networks over 10 days, highly similar to the genetically matched control. Day 1 to 10 post thaw; 100X magnification.
ioGlutamatergic Neurons SNCA A53T/WT demonstrate gene expression of neuronal-specific and glutamatergic-specific markers following deterministic programming
Gene expression analysis demonstrates that ioGlutamatergic Neurons SNCA A53T/WT (clone 621P2D1) and wild-type ioGlutamatergic Neurons (WT Control) lack the expression of pluripotency markers (NANOG and OCT4) at day 11, whilst robustly expressing pan-neuronal (TUBB3 and SYP) and glutamatergic-specific (VGLUT1 and VGLUT2) markers, as well as the glutamate receptor GRIA4. Gene expression levels were assessed by RT-qPCR (data normalised to HMBS; cDNA samples of the parental human iPSC line (hiPSC) were included as reference). Data represents day 11 post-revival samples, n=2 replicates.
The recommended minimum seeding density is 30,000 cells/cm2, compared to up to 250,000 cells/cm2 for other similar products on the market. One small vial can plate a minimum of 0.7 x 24-well plate, 1 x 96-well plate, or 1.5 x 384-well plates. This means every vial goes further, enabling more experimental conditions and more repeats, resulting in more confidence in the data.
Starting material
Human iPSC line
Seeding compatibility
6, 12, 24, 96 & 384 well plates
Shipping info
Dry ice
Donor
Caucasian adult male (skin fibroblast)
Vial size
Small: >1 x 10ⶠviable cells
Quality control
Sterility, protein expression (ICC), gene expression (RT-qPCR) and genotype validation (Sanger sequencing)
Differentiation method
opti-ox deterministic cell programming
Recommended seeding density
30,000 cells/cm²
User storage
LN2 or -150°C
Format
Cryopreserved cells
Product use
ioCells are for research use only
Genetic modification
Heterozygous A53T missense mutation in the SNCA gene
Applications
Parkinson's disease research
Drug discovery and development
Disease modelling
Available clones
io6004: SNCA A53T/WT (621P2B8)
io6005: SNCA A53T/WT (621P2D1)
ÎÞÓǶÌÊÓƵ
V11
ÎÞÓǶÌÊÓƵ
2024
Professor Deepak Srivastava
Professor of Molecular Neuroscience and Group Leader, MRC Centre for Developmental Disorders
King’s College London
Emmanouil Metzakopian | Vice President, Research and Development | ÎÞÓǶÌÊÓƵ
Javier Conde-Vancells | Director Product Management | ÎÞÓǶÌÊÓƵ
Chakraborty et al
Nature Communications
2023
Featuring ioGlutamatergic Neurons
Dr Ania Wilczynska | Head of Computational Genomics | Non-Clinical | ÎÞÓǶÌÊÓƵ
Innovation showcase talk at ISSCR
Marius Wernig MD, PhD | Stanford
Mark Kotter, MD, PhD | ÎÞÓǶÌÊÓƵ
Oosterveen, et al
ÎÞÓǶÌÊÓƵ & Charles River Laboratories
2023
Qiaojin Lin et al
The EMBO Journal
2023
Featuring opti-ox powered hiPSC-derived glutamatergic neurons with constitutive expression of Cas9
Read this blog on glutamatergic neuron cell culture for our top tips on careful handling, cell plating and media changes to achieve success from the outset.
Consistent. Defined. Scalable.