Cathepsin D Stably Over-expressing SH-SY5Y Cell Line
| Unit |
1×10⁶ cells / 1.0 ml |
|---|---|
| Cell Type |
Stable (KO/Expressing) Cells |
| Tissue Type |
Nerve |
| Organism |
Human (H. sapiens) |
| Donor History |
Female ,4 ,Neuroblastoma |
| Growth Properties |
Adherent ,epithelial |
| Growth Conditions |
PriCoat™ T25 Flasks (G299) or Applied Cell Extracellular Matrix (G422) are recommended for optimal cell culture. 1:1 mixture of Prigrow VIII Medium (TM018) and PriGrow XVII Medium (TM029) + 10% FBS + 1% L-Glutamine (G275) + 1% Penicillin/Streptomycin Solution (G255) ,37.0°C ,5% CO₂.Note: Cells are sensitive to trypsin; Gentle Dissociation Solution (TM080) is recommended for subculture procedures. |
| Immortalization Method | |
| Full Information |
This cell line was developed using the Tet-On gene expression system to enable tetracycline-inducible overexpression of Cathepsin D (CD). The human neuroblastoma SH-SY5Y cells were initially transfected with the pcDNA6/TR© vector and subsequently with vectors containing Cathepsin D cDNA. Stable expression was achieved by selecting with blasticidin, followed by induction with tetracycline. Cells express high levels of enzymatically active Cathepsin D when induced, which is shown to reduce the proliferative potential of the cells, possibly through downregulation of the pro-oncogenic MAPK signaling pathway. Ideal for studying the anti-proliferative effects of Cathepsin D in neuroblastoma, the interaction with EGFR signaling, and exploring new therapeutic approaches involving the manipulation of lysosomal enzymes.Additional cell lines from this panel: T3529 – Cathepsin D Stable Knockout SH-SY5Y Cell Line
Mikrobiologické aplikace
NGS
Rapid testy
PCR plasty
Třepačky
Suché lázně
Fluorometry
Buněčné kultury
PCR, qPCR, RT
Detekce Mycoplasmat
Reverzní transkripce
Alergie
Intolerance
Elisa
Imunologické analyzátory
Veterinární imunologie
Alergie u zvířat
Intolerance u zvířat
Biochemie
Imunoanalýza
