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Human PTH1R (Luc) HEK293 Reporter Cell

For research use only.

  1. Genetically modified cell lines best reflect MOA (Mechanism of Action)
  2. Higher activity and larger assay window for robust and reproducible cell-based bioassay
  3. Comprehensive application data to support assay development and validation
  4. Full tracible record, stringent quality control and validated cell passage stability
  5. Parental cell line legally obtained from internationally recognized cell resource bank and commercially licensed
  6. Global commercial license assistance whenever regulatory filing is required

描述(Description)

The Human PTH1R (Luc) HEK293 Reporter Cell was engineered to not only express CREB signaling response element, but also express the receptor full length human PTH1R (Gene ID:5745). which can drive luciferase expressing systems by PTH1R agonists or PTH stimulation. In the absence of agonist or PTH, the PTH1R receptor is not activated and luminescence signal is low. In the presence of agonist or PTH, the PTH1R pathway-activated luminescence can be detected in a dose-dependent manner.

应用说明(Application)

Screen for agonists that can bind and activate PTH1R

PTH1R Assay Principles

生长特性(Growth Properties)

Adherent

筛选标记(Selection Marker)

Puromycin (2 μg/mL) + Hygromycin (20 μg/mL)

培养基(Culture Medium)

DMEM + 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.

 

Application

PTH1R APPLICATION

Bioactivity analysis of human PTH1R agonist (RLU).
This reporter cell was incubated with serial dilutions of human PTH1R agonist. The EC50 of human PTH1R agonist (Teriparatide) was approximately 0.00008739 nM.

Protocol

PTH1R APPLICATION

Bioactivity analysis of human PTH1R agonist (FOLD).
This reporter cell was incubated with serial dilutions of human PTH1R agonist. The max induction fold of human PTH1R agonist (Teriparatide) was approximately 50.51.

Protocol

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背景(Background)

AC2371C1

 

Limited Use&License Disclosure

  1. This cell line is provided for research use only. It is neither intended for any animal or human therapeutic use nor for any direct human in vivo use. You are restricted to share, modify, transfer, distribute, sell, sublicense, or otherwise make the cell line available for use to other researchers, laboratories, research institutions, hospitals, universities, or service organizations.
  2. ACROBIOSYSTEMS MAKES NO WARRANTIES OR REPRESENTATIONS OF ANY KIND, EITHER EXPRESSED OR IMPLIED, WITH RESPECT TO THE SUITABILITY OF THE CELL LINE FOR ANY PARTICULAR USE.
  3. ACROBIOSYSTEMS ACCEPTS NO LIABILITY IN CONNECTION WITH THE HANDLING OR USE OF THE CELL LINE.
  4. Modifications of the cell line, transfer to a third party, or commercial use of the cell line may require a separate license and additional fees. Please contact order.cn@acrobiosystems.com for further details.

 

前沿进展

 
 
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PTH1R靶点信息
英文全称:Parathyroid hormone receptor
中文全称:甲状旁腺激素受体
种类:Homo sapiens
上市药物数量:22详情
临床药物数量:27详情
最高研发阶段:批准上市
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