Human GPR137 knockout U-2 OS cell line
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GPR137 KO cell line available to order. KO validated by Next Generation Sequencing. Free of charge wild type control provided. Knockout achieved by CRISPR/Cas9 X = 1 bp deletion Frameshift: 100%.
View Alternative Names
C11orf4, G protein coupled receptor 137, G protein coupled receptor ORF4, G137A_HUMAN, GPCR ORF4, GPR137, GPR137A, Integral membrane protein GPR137, TM7SF1L1, Transmembrane 7 superfamily member 1-like 1 protein
- NGS
Supplier Data
Next Generation Sequencing - Human GPR137 knockout U-2 OS cell line (AB277179)
Knockout achieved by CRISPR/Cas9; X = 1 bp deletion; Frameshift : 100%
Reactivity data
Product details
Recommended control: Human wild-type U-2 OS cell line (ab263976). Please note a wild-type cell line is not automatically included with a knockout cell line order, if required please add recommended wild-type cell line at no additional cost using the code WILDTYPE-TMTK1.
We will provide viable cells that proliferate on revival.
This product is subject to limited use licenses from The Broad Institute and ERS Genomics Limited, and is developed with patented technology. For full details of the limited use licenses and relevant patents please refer to our limited use license and patent pages.
What's included?
Properties and storage information
Gene name
Gene editing type
Gene editing method
Knockout validation
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Handling procedures
Initial handling guidelines
Upon arrival, the vial should be stored in liquid nitrogen vapor phase and not at -80°C. Storage at -80°C may result in loss of viability.
1. Thaw the vial in 37°C water bath for approximately 1-2 minutes.
2. Transfer the cell suspension (0.8 mL) to a 15 mL/50 mL conical sterile polypropylene centrifuge tube containing 8.4 mL pre-warmed culture medium, wash vial with an additional 0.8 mL culture medium (total volume 10 mL) to collect remaining cells, and centrifuge at 201 x g (rcf) for 5 minutes at room temperature. 10 mL represents minimum recommended dilution. 20 mL represents maximum recommended dilution.
3. Resuspend the cell pellet in 5 mL pre-warmed culture medium and count using a haemocytometer or alternative cell counting method seed all remaining cells into a T25.
4. Incubate the culture at 37°C incubator with 5% CO2. Check the culture one day after revival and continue to check until 80% confluent. Media change can be given if needed.
5. Once confluent passage into an appropriate flask at a density of 2x104 cells/cm2. Seeding density is given as a guide only and should be scaled to align with individual lab schedules. Cultures should be monitored daily.
Subculture guidelines
- All seeding densities should be based on cell counts gained by established methods.
- A guide seeding density of 2x104 cells/cm2 is recommended.
- Cells should be passaged when they have achieved 80-90% confluence.
Culture medium
McCoY5a + 10% FBS
Cryopreservation medium
Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Researchers identify GPR137 as a protein involved in modulating cellular growth survival and differentiation. It functions as a critical part of cellular signaling networks often forming complexes with other receptor proteins to enhance or inhibit signaling pathways. In some studies GPR137 has shown associations with cellular processes like autophagy and apoptosis indicating its importance in maintaining cellular homeostasis. Its expression in multiple tissues suggests it may perform diverse functions depending on the tissue type.
Pathways
Several studies have linked GPR137 to the mTOR signaling and Wnt pathways. These pathways are essential for cell growth proliferation and differentiation. GPR137 interacts with components like mTORC1 in the mTOR signaling pathway which influences protein synthesis and energy metabolism. In the Wnt pathway GPR137 may work alongside proteins like β-catenin contributing to the regulation of gene expression. Understanding its role in these pathways can provide valuable insight into its functions and interactions with other cellular components.
Quality control
STR analysis
CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX
Cell culture
Biosafety level
EU: 1 US: 1
Adherent/suspension
Adherent
Gender
Female
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com