Quick-Glia™ Astrocytes - Human iPSC-derived Astrocytes Healthy Control - (F, 21yr, Asian)

Cryopreserved human iPSC-derived astrocytes from healthy control (F, 21)
As low as ¥342,000.00
Our proprietary transcription factor-based stem cell differentiation method produces highly pure populations of astrocytes without a genetic footprint. Quick-Glia™ Astrocytes - Human iPSC-derived Astrocytes display typical astrocyte morphology and markers such as S100 Calcium Binding Protein β (S100β), Chondroitin Sulfate Proteoglycan 8 (CD44), Aldehyde Dehydrogenase 1 Family Member L1 (ALDH1L1), and mature astrocyte marker Glial Fibrillary Acidic Protein (GFAP). When handled and maintained according to the instructions in this user guide, astrocytes are viable long-term and are suitable for a variety of characterization and neurotoxicity assays.
More Information
Short Description Cryopreserved human iPSC-derived astrocytes from healthy control (F, 21)
Product Components Cryopreserved cells and Component P
Starting Material iPSCs derived from peripheral blood mononuclear cells (CIRM line CW70067)
Product Use This product is for research use only. It is not approved for use in humans or for therapeutic or diagnostic use.
Storage Conditions Frozen cells should be stored in liquid (vapor phase). The rest of the components should be stored at -20°C.
Cell Type Astrocytes
Culture Type Feeder Cell-Free
Disease Healthy Control
Donor Sex Female
Donor Race Ethnicity Asian
Patient History See Resources section for more information.
Reprogramming Method Episomal vector
Induction Method Transcription factors delivered by Sendai virus
Growth Properties Adherent
Shipping Conditions Dry ice (domestic) or liquid nitrogen (international)
Shelf Life 1 year
Donor Age At Sampling 21




いいえ。当社の分化キットやiPS細胞由来分化細胞を使用するのに、追加ライセンスやMTA(Material Transfer Agreement)は必要ありません。ただし、これらの製品は研究用に限ります。 一方、mRNAのCDMOサービスについては個別の案件で異なりますので、問い合わせください。






Quick-Tissue™技術で使用されるセンダイウイルス(SeV)はRNAウイルスですので、ゲノムDNAに組み込まれることはありません。、原則として、RNAとして細胞に導入された外来遺伝子は、またmRNAで導入された場合でも、DNAと違い細胞核内に入り込む必要がなく、すぐさま翻訳され発現されます。よって、ゲノム上の遺伝子を変異させることはありません。これは以下の総説で論じられています。Yamamoto, et al. (2009) "Current prospects for mRNA gene delivery." Eur. Eur.J. Pharm Biopharm 71, 484-489.