CHO-K1 Human GPR183（EBI2）β-Arrestin Cell Line
Cat. No： RQP71487
Size： 1 vial of frozen cells (>1E6 per vial in 1 mL)
Unit Price： Contact For Pricing
Description
Product Info
Biological Information
Assay Data
Cell Culture
This product is a CHO-K1 stable β-Arrestin cell line that stably expresses human GPR183(EBI2) receptor. Upon agonist binding to GPR183(EBI2), receptor phosphorylation occurs and recruits β-arrestin, reconstituting the split luciferase reporter system and generating luminescent signals. Therefore, receptor activity can be easily quantified in live cells in a dose-response manner by measuring luminescence intensity. This cell line is suitable for high-throughput screening (HTS) and receptor functional evaluation assays.
| Cat. No | RQP71487 |
| Product Name | CHO-K1 Human GPR183（EBI2）β-Arrestin Cell Line |
| Engineering method | plasmid and lentivirus |
| Culture Properties | Adherent |
| Stability | 32passages (in-house test, that not means the cell line will be instable beyond the passages we tested.) |
| Mycoplasma Status | Negative |
| Culture Medium | F12K+10%FBS+5 μg/ml puromycin+5 μg/ml blasticidin |
| Freeze Medium | 90% FBS+10% DMSO |
| Storage Conditions | Liquid nitrogen immediately upon delivery |
| Transducer | β-Arrestin |
| Application | Functional assay for GPR183 |
| Safety Precautions |
Wear lab coat, disposable gloves to avoid direct sample contact. For spills: apply disinfectant, allow full inactivation, then clean up. |
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.
| Target Class | GPCR |
| Family | G protein-coupled receptors |
| Sub Family | Class A（Rhodopsin） |
| Gene Name | GPR183 |
| Gene Aliases | EBI2;Epstein-Barr virus induced gene 2;EBV-induced G-protein coupled receptor 2 |
| Gene ID | 1880 |
| Accession Number | NM_004951 |
| UniProt Number | P32249 |
| Protein Name | G-protein coupled receptor 183 |
| Protein Aliases | Epstein-Barr virus-induced G-protein coupled receptor 2;EBI2;EBV-induced G-protein coupled receptor 2;hEBI2 |
| Target Species | Human |
| Host cell | CHO-K1 |
Figure 1. Recombinant GPR183（EBI2）β-Arrestin CHO-K1 stably expressing GPR183
Blue curve: GPR183(EBI2) β-Arrestin CHO Cells(C5) stained with anti-GPR183 antibody, median FL4-A =8.50E5. Red curve: parental CHO cell control stained with anti-GPR183 antibody, median FL4-A =997. The obvious fluorescence shift demonstrates high GPR183 expression on the cell membrane.
Figure 2. Dose Response of 7α，25-DihydroxyCHO-K1lesterol in GPR183（EBI2）β-Arrestin CHO-K1(C5)
The luminescence signal (RLU) reflects β-arrestin recruitment upon receptor activation. 7α,25-Dihydroxycholesterol induces β-arrestin recruitment in a dose-dependent manner, with EC₅₀ = 10.7 nM and S/B = 85.1
Cell Resuscitation
1)Rapidly thaw the frozen cells in a 37 °C water bath for approximately 60 seconds. Once thawed (which may take slightly less or more than 60 seconds), immediately transfer the cell suspension from the cryovial into a 15 mL centrifuge tube containing 10 mL of pre-warmed CHO-K1 Human GPR183（EBI2）β-Arrestin Cell Line complete culture medium.
2)Centrifuge cells at 1000 rpm for 5 min to remove medium, then resuspend cells in 5 mL of pre-warmed complete medium.
3)Transfer the cell suspension into a T25 culture flask and incubate at 37 °C with 5% CO₂.
4)After approximately 24–36 hours, replace the medium or passage the cells to remove non-adherent dead cells.
Subculturing procedure
1)When the cell density reaches the appropriate confluency for passaging, wash the cells with PBS, then add 1 mL trypsin to detach the cells. When more than 80% of the cells detach upon gently tapping the culture flask, add complete culture medium to terminate digestion. Gently pipette to obtain a single-cell suspension, transfer to a 15 mL centrifuge tube, and centrifuge at 1000 rpm for 5 minutes.
2)Discard supernatant after centrifugation. Resuspend cells in fresh medium to a single-cell suspension and transfer to a new culture flask for continued growth.
Cell Freezing
After trypsinization and centrifugation of cells from each T75 flask or 10 cm culture dish, discard the supernatant. Add 2 mL of cryopreservation medium (90% FBS + 10% DMSO), gently resuspend thoroughly, and aliquot into two cryovials. Immediately place the cryovials into a controlled-rate freezing container (e.g., Nalgene 5100-0001), fill with isopropanol to the indicated level, and store at −80 °C. After 24 hours, transfer the cryovials to liquid nitrogen for long-term storage.