收藏产品 产品信息
- Genetically modified cell lines best reflect MOA (Mechanism of Action)
- Higher activity and larger assay window for robust and reproducible cell-based bioassay
- Comprehensive application data to support assay development and validation
- Full tracible record, stringent quality control and validated cell passage stability
- Parental cell line legally obtained from internationally recognized cell resource bank and commercially licensed
- Global commercial license assistance whenever regulatory filing is required
描述（Description）
The CHO/ Cynomolgus Glypican-3 (GPC3) Stable Cell Line was engineered to express the receptor full length Cynomolgus Glypican-3 (Gene ID:9541). Surface expression of Cynomolgus Glypican-3 was confirmed by flow cytometry.
应用说明（Application）
• Useful for cell-based Glypican-3 binding assay
生长特性（Growth Properties）
Adherent
筛选标记（Selection Marker）
Hygromycin B (20 μg/mL)
培养基（Complete Growth Medium）
F-12K + 10% FBS
冻存液（Freeze Medium）
Serum-free cell cryopreservation medium
装量（Quantity）
1 vial contains at least 5×10^6 cells in 1 mL serum-free cryopreservation medium
存储（Storage）
Frozen in liquid nitrogen.
支原体检测（Mycoplasma Testing）
Negative
无菌检测（Sterility Testing）
Negative
使用说明（Instructions for Use）
See data sheet for detailed culturing and assay protocol.
产品数据图
Receptor Assay
Expression analysis of Cynomolgus Glypican-3 (GPC3) on CHO/Cynomolgus Glypican-3 (GPC3) Stable Cell Line by FACS.
Cell surface staining was performed on CHO/Cynomolgus Glypican-3 (GPC3) Stable Cell Line or negative control cell using anti-Cynomolgus Glypican-3 (GPC3) Antibody followed by staining with PE anti-human IgG Fc Antibody.
Protocol
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背景
Glypican-3 (GPC3) is also known as Intestinal protein OCI-5, GTR2-2, MXR7, which belongs to the glypican family. Glypican 3 / GPC-3 is highly expressed in lung, liver and kidney. Glypican-3 inhibits the dipeptidyl peptidase activity of DPP4. Glypican-3 may be involved in the suppression/modulation of growth in the predominantly mesodermal tissues and organs, and also may play a role in the modulation of IGF2 interactions with its receptor and thereby modulate its function.
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