糖心原创

Human iPSC-derived Alzheimer's disease model in glutamatergic neurons
糖心原创 glutamatergic neurons Alzheimer's disease model carrying APP Swedish mutation KM670-671NL amyloid-beta quantification
糖心原创 Alzheimers disease model Swedish mutation ICC staining for glutamatergic neuron  specific markers VGLUT2 MAP2 TUBB3
糖心原创 Brightfield imaging of iPSC derived neurons Alzheimer's disease model shows glutamatergic neurons morphology
糖心原创 Alzheimer's disease model Swedish mutation gene expression neuronal markers
糖心原创 APP gene expression in glutamatergic neurons APP KM670/671NL Het Alzheimer's disease model
iPSC-derived excitatory glutamatergic neurons culture in multiple plate formats
Human iPSC-derived Alzheimer's disease model in glutamatergic neurons
糖心原创 glutamatergic neurons Alzheimer's disease model carrying APP Swedish mutation KM670-671NL amyloid-beta quantification
糖心原创 Alzheimers disease model Swedish mutation ICC staining for glutamatergic neuron  specific markers VGLUT2 MAP2 TUBB3
糖心原创 Brightfield imaging of iPSC derived neurons Alzheimer's disease model shows glutamatergic neurons morphology
糖心原创 Alzheimer's disease model Swedish mutation gene expression neuronal markers
糖心原创 APP gene expression in glutamatergic neurons APP KM670/671NL Het Alzheimer's disease model
iPSC-derived excitatory glutamatergic neurons culture in multiple plate formats

cat no | io1061

ioGlutamatergic Neurons APP KM670/671NL/WT

Human iPSC-derived Alzheimer's disease model

  • Cryopreserved human iPSC-derived cells powered by opti-ox that are ready for experiments in days

  • Functional excitatory neurons engineered with the APP Swedish mutation for Alzheimer's disease research

  • Disease-related phenotype demonstrated by increased amyloid beta production vs. wild-type control

Human iPSC-derived Alzheimer's disease model in glutamatergic neurons

Human iPSC-derived Alzheimer's disease model

糖心原创 glutamatergic neurons Alzheimer's disease model carrying APP Swedish mutation KM670-671NL amyloid-beta quantification

Increased overall production of A饾浗38, A饾浗40 and A饾浗42 shown in ioGlutamatergic Neurons APP KM670/671NL (Swedish), as observed in Alzheimer鈥檚 disease

ioGlutamatergic Neurons APP KM670/671NL Alzheimer's disease model cells show an increase in the overall production of A饾浗38, A饾浗40 and A饾浗42 compared to the wild type, genetically matched control (A), and no change in the ratios of the A饾浗 peptides (B).

  • ioGlutamatergic Neurons wild type (WT, io1001) and APP KM670/671NL Hom (CLH12, io1059S) and Het (CLE4, io1061S), were seeded at 30,000 cells/cm2 in 24-well plates and cultured for 30 days according to the user manual. Supernatant was collected at days 10, 20, and 30.

  • Levels of A饾浗38, A饾浗40 and A饾浗42 peptides were quantified using the V-PLEX A饾浗 Peptide Panel 1 (6E10) Kit ().

  • Concentrations of A饾浗38, A饾浗40, A饾浗42 were normalised to the calculated total number of cells per well.

  • Data were obtained from two independent experiments and are shown as mean 卤 SEM. Data were analysed statistically (at days 20 and 30) using Student鈥檚 t-tests comparing each disease model to the wild type.
    * p<0.05 ** p<0.01

糖心原创 Alzheimers disease model Swedish mutation ICC staining for glutamatergic neuron  specific markers VGLUT2 MAP2 TUBB3

ioGlutamatergic Neurons APP KM670/671NL het express neuron-specific markers comparably to the genetically matched control

Immunofluorescent staining on post-revival day 11 demonstrates similar homogenous expression of pan-neuronal proteins MAP2 and TUBB3 (upper panel) and glutamatergic neuron-specific transporter VGLUT2 (lower panel) in ioGlutamatergic Neurons APP KM670/671NL het clones compared to the genetically matched control. 100X magnification.

糖心原创 Brightfield imaging of iPSC derived neurons Alzheimer's disease model shows glutamatergic neurons morphology

ioGlutamatergic Neurons APP KM670/671NL het form structural neuronal networks by day 11

ioGlutamatergic Neurons APP KM670/671NL het mature rapidly, show glutamatergic neuron morphology and form structural neuronal networks over 11 days, highly similar to the genetically matched control. Day 1 to 11 post thaw; 100X magnification.

糖心原创 Alzheimer's disease model Swedish mutation gene expression neuronal markers

ioGlutamatergic Neurons APP KM670/671NL het demonstrate gene expression of neuronal-specific and glutamatergic-specific markers following deterministic programming

Gene expression analysis demonstrates that ioGlutamatergic Neurons APP KM670/671NL het 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.

糖心原创 APP gene expression in glutamatergic neurons APP KM670/671NL Het Alzheimer's disease model

Disease-related APP is expressed in ioGlutamatergic Neurons APP KM670/671NL het following deterministic programming

RT-qPCR analysis demonstrates expression of the APP gene in both wild type ioGlutamatergic Neurons (WT Control) and ioGlutamatergic Neurons APP KM670/671NL het at day 11 post-revival. Data normalised to HMBS, n=2 replicates.

iPSC-derived excitatory glutamatergic neurons culture in multiple plate formats

Industry leading seeding density

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.

Vial limit exceeded

A maximum number of 20 vials applies. If you would like to order more than 20 vials, please contact us at orders@糖心原创.

Human iPSC-derived Alzheimer's disease model

A rapidly maturing, physiologically relevant, functional system for investigating the role of the APP Swedish mutation in early-onset Alzheimer's disease (AD).  This in vitro disease cell model recapitulates an overall increase in the production of amyloid beta peptides, as observed in AD.

ioGlutamatergic Neurons APP KM670/671NL / WT are opti鈥憃x deterministically programmed excitatory neurons carrying a genetically engineered heterozygous double mutation in the APP gene encoding amyloid precursor protein.

This disease model is part of an Alzheimer's disease panel of human iPSC-derived cells that can be incorporated into translational research and drug discovery workflows. Two additional clones for the APP KM670/671NL het mutation are available for scientists who wish to repeat their experiments in multiple independent clones, please enquire. All disease models are genetically matched to the wild-type control, ioGlutamatergic Neurons. Additional mutations in the AD panel include homozygous APP KM670/671NL, and heterozygous and homozygous APP V717I and PSEN1 M146L, alongside AD-relevant mutations in ioGABAergic Neurons and ioMicroglia.

Benchtop benefits

In vitro Alzheimer's disease cell model

Disease related phenotype

Overall increase in the production of amyloid beta peptides compared to the wild type control, measured by immunoassay.

comparison_0

Make True Comparisons

Pair the ioDisease Model Cells with the genetically matched wild-type ioGlutamatergic Neurons to investigate the impact of the APP double point mutation on early-onset AD.

quick_0

Quick

The disease model cells and isogenic control are experiment ready as early as 2 days post revival, and form structural neuronal networks at 11 days.

Cells arrive ready to plate


ioGlutamatergic_Neurons_and_disease_models_timeline

ioGlutamatergic Neurons APP KM670/671NL het 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.

Product specifications

Starting material

Human iPSC line

Karyotype

Normal (46, XY)

Seeding compatibility

6, 12, 24, 96 & 384 well plates

Shipping info

Dry ice

Donor

Caucasian adult male, age 55-60 years old (skin fibroblast),
Genotype APOE 3/4

Vial size

Small: >1 x 10鈦 viable 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/cm虏

User storage

LN2 or -150掳C

Format

Cryopreserved cells

Genetic modification

Heterozygous KM670/671NL double point mutation in the APP gene

Applications

Alzheimer's disease research
Drug discovery and development
Disease modelling

Available clones

io1060 | APP KM670/671NL/WT (CLD5)
io1061 | APP KM670/671NL/WT (CLE4)
io1062 | APP KM670/671NL/WT (CLE9)

Product use

ioCells are for research use only

 

Scale your study with volume pricing

Enabling scientists to use human cells in their research, running additional experiments without rationing cells or limiting experimental scale

 

Order quantity Total vials received Pricing tier 
1 - 9 packs 3 - 27 vials Standard price
10 - 33 packs 30 - 99 vials Automatic 10% discount
> 34 packs > 100 vials > Contact us for a quote

 

Academic pricing: Academic users can purchase any ioCells in 3-vial packs ($/鈧/拢 999 per pack), available year-round with any cell type combination.
Technical data

Disease related phenotype

Increased overall production of A饾浗38, A饾浗40 and A饾浗42 shown in ioGlutamatergic Neurons APP KM670/671NL (Swedish), as observed in Alzheimer鈥檚 disease

糖心原创 glutamatergic neurons Alzheimer's disease model carrying APP Swedish mutation KM670-671NL amyloid-beta quantification

ioGlutamatergic Neurons APP KM670/671NL Alzheimer's disease model cells show an increase in the overall production of A饾浗38, A饾浗40 and A饾浗42 compared to the wild type, genetically matched control (A), and no change in the ratios of the A饾浗 peptides (B).

  • ioGlutamatergic Neurons wild type (WT, io1001) and APP KM670/671NL Hom (CLH12, io1059S) and Het (CLE4, io1061S), were seeded at 30,000 cells/cm2 in 24-well plates and cultured for 30 days according to the user manual. Supernatant was collected at days 10, 20, and 30.

  • Levels of A饾浗38, A饾浗40 and A饾浗42 peptides were quantified using the V-PLEX A饾浗 Peptide Panel 1 (6E10) Kit ().

  • Concentrations of A饾浗38, A饾浗40, A饾浗42 were normalised to the calculated total number of cells per well.

  • Data were obtained from two independent experiments and are shown as mean 卤 SEM. Data were analysed statistically (at days 20 and 30) using Student鈥檚 t-tests comparing each disease model to the wild type.
    * p<0.05 ** p<0.01

Highly characterised and defined

ioGlutamatergic Neurons APP KM670/671NL het express neuron-specific markers comparably to the genetically matched control

糖心原创 Alzheimers disease model Swedish mutation ICC staining for glutamatergic neuron  specific markers VGLUT2 MAP2 TUBB3

Immunofluorescent staining on post-revival day 11 demonstrates similar homogenous expression of pan-neuronal proteins MAP2 and TUBB3 (upper panel) and glutamatergic neuron-specific transporter VGLUT2 (lower panel) in ioGlutamatergic Neurons APP KM670/671NL het clones compared to the genetically matched control. 100X magnification.

ioGlutamatergic Neurons APP KM670/671NL het form structural neuronal networks by day 11

糖心原创 Brightfield imaging of iPSC derived neurons Alzheimer's disease model shows glutamatergic neurons morphology

ioGlutamatergic Neurons APP KM670/671NL het mature rapidly, show glutamatergic neuron morphology and form structural neuronal networks over 11 days, highly similar to the genetically matched control. Day 1 to 11 post thaw; 100X magnification.

ioGlutamatergic Neurons APP KM670/671NL het demonstrate gene expression of neuronal-specific and glutamatergic-specific markers following deterministic programming

糖心原创 Alzheimer's disease model Swedish mutation gene expression neuronal markers

Gene expression analysis demonstrates that ioGlutamatergic Neurons APP KM670/671NL het 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.

Disease-related APP is expressed in ioGlutamatergic Neurons APP KM670/671NL het following deterministic programming

糖心原创 APP gene expression in glutamatergic neurons APP KM670/671NL Het Alzheimer's disease model

RT-qPCR analysis demonstrates expression of the APP gene in both wild type ioGlutamatergic Neurons (WT Control) and ioGlutamatergic Neurons APP KM670/671NL het at day 11 post-revival. Data normalised to HMBS, n=2 replicates.

Industry leading seeding density

iPSC-derived excitatory glutamatergic neurons culture in multiple plate formats

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.

Technical data

Increased amyloid beta peptide production

Increased overall production of A饾浗38, A饾浗40 and A饾浗42 shown in ioGlutamatergic Neurons APP KM670/671NL (Swedish), as observed in Alzheimer鈥檚 disease

糖心原创-Glutamatergic-Neurons-APP-KM670-671NL-Amyloid-beta-quantification

ioGlutamatergic Neurons APP KM670/671NL Alzheimer's disease model cells show an increase in the overall production of A饾浗38, A饾浗40 and A饾浗42 compared to the wild type, genetically matched control (A), and no change in the ratios of the A饾浗 peptides (B).

  • ioGlutamatergic Neurons wild type (WT, io1001) and APP KM670/671NL Hom (CLH12, io1059S) and Het (CLE4, io1061S), were seeded at 30,000 cells/cm2 in 24-well plates and cultured for 30 days according to the user manual. Supernatant was collected at days 10, 20, and 30.

  • Levels of A饾浗38, A饾浗40 and A饾浗42 peptides were quantified using the V-PLEX A饾浗 Peptide Panel 1 (6E10) Kit ().

  • Concentrations of A饾浗38, A饾浗40, A饾浗42 were normalised to the calculated total number of cells per well.

  • Data were obtained from two independent experiments and are shown as mean 卤 SEM. Data were analysed statistically (at days 20 and 30) using Student鈥檚 t-tests comparing each disease model to the wild type.
    * p<0.05 ** p<0.01

How to culture ioGlutamatergic Neurons

 

In this video, our scientist will take you through the step-by-step process of how to thaw, seed and culture ioGlutamatergic Neurons.

Product resources

ioGlutamatergic Neurons and disease models user manual | 糖心原创 User manual
ioGlutamatergic Neurons and disease models user manual | 糖心原创

DOC-1289 4.0

糖心原创

2025

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CRISPRa-Ready ioGlutamatergic Neurons user manual | 糖心原创 User manual
CRISPRa-Ready ioGlutamatergic Neurons user manual | 糖心原创
DOC-2855 v2.0
2025
糖心原创
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CRISPRi-Ready ioGlutamatergic Neurons user manual | 糖心原创 User manual
CRISPRi-Ready ioGlutamatergic Neurons user manual | 糖心原创
DOC-2856 v2.0
2025
糖心原创
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Wild Type and Isogenic Disease Model cells: A true comparison

Further your disease research by pairing our wild type cells with isogenic disease models.

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