Thermo Scientific™ GeneBLAzer™ CCKAR HEK 293T DA Assay Kit
Manufacturer: Thermo Scientific™
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | K1623-Each-of-1 | In Stock | ₹ 98,736.24 |
K1623 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 98,736.24
GST (18%): ₹ 17,772.523
Total Price: ₹ 1,16,508.763
Accession Number
NM_000730.2
Cell State
Division-Arrested Cells
Detection Method
Fluorescence
Population Status
Single Cell Clone Origin
Quantity
8 x 106Cells
Target Entry
CCKAR
System Type
GeneBLAzer™
Assay Entry
Cell-based beta lactamase reporter gene
Content And Storage
Each kit contains sufficient quantities of division arrested (DA) cells and substrate to assay 1 x 384 well plate. (Other materials are required separately; please refer to the protocol).Includes:• GeneBLAzer™ CCKAR HEK 293T DA cells• LiveBLAzer™-FRET B/G Loading Kit, 70 μg• Solution D• GeneBLAzer™ CCKAR HEK 293T DA Assay Protocol• LiveBLAzer™-FRET B/G Loading Protocol• Certificate of AnalysisThe GeneBLAzer™ CCKAR HEK 293T DA cells are shipped on dry ice and should be stored in liquid nitrogen immediately upon receipt.
Gene Symbol
CCKAR
Product Line
GeneBLAzer™
Reporter Gene
BLA (Beta-Lactamase)
Cell Line
293T (HEK)
Druggable Target
GPCR
Related Products
Description
- Description The GeneBLAzer™ CCKAR-NFAT-bla CHO-K1 cells contain the human Cholecystokinin A Receptor (CCKAR) stably integrated into the GeneBLAzer™ NFAT-bla CHO-K1 cell line
- GeneBLAzer™ NFAT-bla CHO-K1 (Cat
- No
- K1447) contains a beta-lactamase (bla) reporter gene under control of a NFAT response element stably integrated into CHO-K1 cells
- The CCKAR-NFAT-bla CHO-K1 cells are functionally validated for Z'-factor and EC50 concentrations using established ligands
- In addition, CCKAR-NFAT-bla CHO-K1 cells have been tested for assay performance under variable conditions
- These data are found in the Validation & Assay Performance Summary
- Division Arrested cells are irreversibly division arrested using a low-dose treatment of Mitomycin C, and have no apparent toxicity or change in cellular signal transduction.