Stem Cells

HighQC™ Human IPSC-Derived Neural Stem Cell LRRK2 G2019S HET

  • For research use only

Cat No.

ABC-SC0068T

Product Type

Human iPSCs

Cell Type

Neural Stem Cell

Species

Human

Growth Conditions

37 ℃, 5% CO2

Source Organ

iPSC

Disease

Normal

Storage

Liquid Nitrogen

HighQC™ Human IPSC-Derived Neural Stem Cell LRRK2 G2019S HET supports Parkinson’s disease modeling, LRRK2 pathway analysis, and neurodegeneration research.

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Description

HighQC™ Human IPSC-Derived Neural Stem Cells-LRRK2 G2019S HET are a neural stem cell line derived from human iPSCs with a heterozygous G2019S mutation introduced into the LRRK2 gene using CRISPR-Cas9 gene editing. One allele carries the mutation, while the other remains wild-type at the locus. These neural stem cells express PAX6, FOXG1, and Nestin. The G2019S variant is associated with increased kinase activity, mitochondrial abnormalities, and lysosomal dysfunction in dopaminergic neurons. These cells are valuable for studying gene dosage effects, neuronal vulnerability, and pharmacological correction of LRRK2-related phenotypes. They are suitable for in vitro modeling of disease initiation and progression. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from HIV-1, HBV, HCV, Syphilis, Mycoplasma, Fungi, Yeast, and Bacteria.
Product Code

HighQC™ Human IPSC-Derived Neural Stem Cell LRRK2 G2019S HET, hIPSC-NSC-LRRK2-G2019S-HET, Human IPSC Neural Stem Cells Parkinson LRRK2 Heterozygous

Species

Human

Cat.No

ABC-SC0068T

Product Category

Stem Cells

Size/Quantity

1 vial

Cell Type

Neural Stem Cell

Growth Mode

Adherent

Shipping Info

Dry Ice

Growth Conditions

37 ℃, 5% CO2

Source Organ

iPSC

Disease

Normal

Storage

Liquid Nitrogen

Product Type

Human iPSCs

Application

  • These LRRK2 G2019S heterozygous iPSC-Derived NSCs enables analysis of gene dosage effects in Parkinson’s disease. It supports studies of early cellular pathology, kinase activity modulation, and mitochondrial dysfunction. Ideal for testing therapeutic agents targeting the LRRK2 pathway and its downstream effects on neuron survival. Its heterozygous nature closely mirrors the genetic profile of most patients with this mutation, enhancing the translational relevance of research findings.

Citation

When you publish your research, please cite our product as "AcceGen Biotech Cat.# XXX-0000". In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).

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High Viability
To succeed in cell culture
Precision and Reliability
To support a consistent result
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Tailed to your research

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