General

Cell Line

hPSCreg name SCTi003-A-2
Cite as:
SCTi003-A-2
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines No similar lines found.
Last update 26th August 2025
Notes Genome-edited Human hiPSC Line, SCTi003-A-2, APP K670N/M671L (Swedish Mutation) (SCTi003-A-2) was generated by CRISPR/Cas9 technology, which introduced the amyloid precursor protein (APP) K670N/M671L double mutation (also known as the Swedish mutation, c.2026A>G & c.2032T>A) into the endogenous APP locus. The Swedish mutation is a well-characterized familial Alzheimer’s disease mutation associated with increased β-secretase cleavage of APP, leading to an elevated production of amyloid-β peptides and early-onset Alzheimer’s pathology (Sasaguri et al.; Thordardottir & Graff).

This product’s parental human induced pluripotent stem cell (hiPSC) line, Healthy Control Human iPSC Line, Female, SCTi003-A, is a well-characterized control line derived from peripheral blood mononuclear cells (PBMCs) from a 48-year-old donor. Targeted gene modifications were confirmed by Sanger sequencing. Post-editing, extensive quality control procedures were undertaken in the manufacturing process for SCTi003-A-2 to ensure optimal product performance and reproducibility. SCTi003-A-2 is karyotypically stable, expresses markers of the undifferentiated state, and remains capable of directed differentiation into all three germ layers, including neural lineage cells relevant for Alzheimer’s disease research. This genome-edited hiPSC line, along with its parental hiPSC line, provides a robust, isogenic disease modeling tool for studying amyloidogenic processing, studying Alzheimer’s disease mechanisms, and evaluating therapeutic interventions targeting the APP pathway.

SCTi003-A-2 is manufactured with mTeSR™ Plus (Catalog #100-0276) and is compatible with STEMdiff™ cell culture media products, allowing for standardized high-quality maintenance and differentiation to various cell types, such as neurons, astrocytes, and microglia.

Cells were obtained using Institutional Review Board (IRB)-approved consent forms and protocols.
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Provider

Generator STEMCELL Technologies Inc. (SCT)
Owner STEMCELL Technologies Inc. (SCT)
Distributors
Derivation country United States

External Databases

BioSamples SAMEA119562656

General Information

* Is the cell line readily obtainable for third parties?
Yes
Research use: allowed
Clinical use: not allowed
Commercial use: allowed
Subclone of

Donor Information

General Donor Information

Sex female
Ethnicity Self-declared race/ethnicity = White
Ancestry = 100% European

Phenotype and Disease related information (Donor)

Diseases No disease was diagnosed.
Is the medical history available upon request? No
Is clinical information available? No

Other Genotyping (Donor)

Is there genome-wide genotyping or functional data available?
No

External Databases (Donor)

BioSamples SAMEA11371632

Ethics

Also have a look at the ethics information for the parental line SCTi003-A .
Is there an MTA available for the cell line? No
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?
Are you aware of any constraints on the use or distribution of the cell line from the owner or any parties identified in the query above? No

hIPSC Derivation

General

The source cell information can be found in the parental cell line SCTi003-A.

Reprogramming method

Vector type Non-integrating
Vector Proprietary non-integrating reprogramming technology
Is reprogramming vector detectable?
No
Methods used
PCR
Notes on reprogramming vector detection Clearance confirmed at passage 21

Vector free reprogramming

Type of used vector free reprogramming factor(s)
None

Other

Derived under xeno-free conditions
No
Derived under GMP?
No
Available as clinical grade?
No

Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Enzyme-free cell dissociation
ReLeSR™
O2 Concentration 20 %
CO2 Concentration 5 %
Medium mTeSR™ Plus
Has Rock inhibitor (Y27632) been used at passage previously with this cell line?
Yes
Has Rock inhibitor (Y27632) been used at cryo previously with this cell line?
No
Has Rock inhibitor (Y27632) been used at thaw previously with this cell line?
No

Characterisation

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
POU5F1 (OCT-4)
Yes
TRA 1-60
Yes
Score:
Marker Present Absent
mCpG
OCT4
Morphology pictures
Figure 2. SCTi003-A-2 Human iPSCs Demonstrate High-Quality Morphology in Routine Culture.

Cryopreserved cells from line SCTi003-A-2 were thawed and maintained in mTeSR™ Plus (Catalog #100-1130) on Corning® Matrigel® Matrix. (A) The resulting iPSC colonies have densely packed cells and show multi-layering when ready to be passaged. (B,C) Cells retain prominent nucleoli and high nuclear-to-cytoplasmic ratios. iPSC = induced pluripotent stem cell.
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro directed differentiation
Marker Expressed
SOX17
Yes
CXCR4
Yes
Protocol or reference
Mesoderm
Ont Id: UBERON_0000926
In vitro directed differentiation
Marker Expressed
TBXT
Yes
NCAM1
Yes
Protocol or reference
Ectoderm
Ont Id: UBERON_0000924
In vitro directed differentiation
Marker Expressed
PAX6
Yes
NES
Yes
Protocol or reference

Microbiology / Virus Screening

HIV 1 Negative
HIV 2 Negative
Hepatitis B Negative
Hepatitis C Negative
Mycoplasma Negative

Certificate of Analysis

Is there a certificate of analysis available?
Yes
Passage: 37

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
46,XX
Passage number: 37
Karyotyping method: G-Banding

Other Genotyping (Cell Line)

Is there genome-wide genotyping or functional data available?
Yes
Exome sequencing
Whole exome sequencing data file (Catalog #500-0707) is available upon request for a fee for SCTi003-A-2 customers. Please contact iPSCrequests@stemcell.com for more information.
SNP typing array
SNP microarray data is included in each lot-specific COA. Please contact iPSCrequests@stemcell.com for more information.
Genome Sequencing
Whole genome sequencing data file (Catalog #500-0708) is available upon request for a fee for SCTi003-A-2 customers. Please contact iPSCrequests@stemcell.com for more information.

Genetic Modification

Disease/phenotype related modifications
Synonyms
  • Alzheimer's Disease
  • Alzheimer disease
  • Alzheimer Disease
  • Alzheimer dementia
  • Alzheimer's Dementia
  • Alzheimer's disease
  • Alzheimer's disease, unspecified
show more synonyms
Genetic modifications
APP - amyloid beta precursor protein (target)
Isogenic modification
21q21.3
NM_000484.4:c.[2010G>C];[2011A>C];[2013G>Y]
NP_000475.1:p.K670N/M671L
Homozygous
The SCTi003-A-2 iPSC line was derived from the parental SCTi003-A line, which originated from a healthy female donor with a wild-type APP genotype. Using CRISPR-Cas9 genome editing, three nucleotide substitutions affecting two consecutive codons in exon 16 of the APP gene (NM_000484.4) were introduced to generate the Swedish mutation (KM670/671NL).

A G>C substitution at c.2010 changes codon 670 from AAG to AAC, resulting in a lysine (Lys) to asparagine (Asn) substitution (K670N). Two additional substitutions at c.2011 (A>C) and c.2013 (G>Y, where Y denotes C/T heterozygosity) change codon 671 from ATG to CTC and CTT on the two alleles, both encoding leucine (Leu) (M671L). At c.2013, heterozygosity produces two equivalent leucine codons, so the variant is functionally homozygous at the protein level.

All three nucleotide changes occur in cis on both alleles, producing a homozygous K670N/M671L genotype at the protein level. This engineered line models the APP Swedish mutation, a well-characterized early-onset familial Alzheimer’s disease variant associated with increased amyloidogenic processing of APP. The homozygous K670N/M671L genotype provides a genetically engineered in vitro system for investigating APP processing and supporting Alzheimer’s disease research.
Mutated