Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-RG0057
Host Cell : HEK293 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RG0057 |
| Target Gene | AVPR2 |
| Gene Species | Homo sapiens (Human) |
| Abbr | HEK293-HuAVPR2-SNAP |
| Alias | AVPR2, DIR, DIR3, V2R, DI1, DIR, NDI, ADHR, DIR3, MGC126533, MGC138386 |
| Host Cell | HEK293 |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1. Gene expression studies 2. Signaling pathway research 3. Drug screening and toxicology 4. Research on the mechanisms of GPCR-related diseases |
| Size | >1x106 frozen cells/vial |
| Stability | Validated for at least 10 passages |
| Quality Control | Negative for bacteria, yeast, fungi and mycoplasma. |
| Storage | Liquid nitrogen |
| Shipping | Dry ice |
| Revival | Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media. |
| Media Type | Cells were cultured in DMEM supplemented with 10% fetal bovine serum. |
| Growth Properties | Cells are cultured as a monolayer at 37°C in a humidified atmosphere with 5% CO2. Split at 80-90% confluence, approximately 1:3-1:6. |
| Freeze Medium | Complete medium supplemented with 10% (v/v) DMSO |
| Morphology | Epithelial |
| Mycoplasma | Negative |
| Format | One frozen vial containing millions of cells |
| Storage | Liquid nitrogen |
| Safety Considerations |
The following safety precautions should be observed. 1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum. 2. No eating, drinking or smoking while handling the stable line. 3. Wash hands after handling the stable line and before leaving the lab. 4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells. 5. All waste should be considered hazardous. 6. Dispose of all liquid waste after each experiment and treat with bleach. |
| Ship | Dry ice |
| Gene Name | AVPR2 arginine vasopressin receptor 2 [ Homo sapiens ] |
| Gene Symbol | AVPR2 |
| Synonyms | DI1; DIR; NDI; V2R; ADHR; DIR3 |
| Gene ID | 554 |
| Uni Prot ID | P30518 |
| m RNA Refseq | NM_000054.4 |
| Protein Refseq | NP_000045.1 |
| Chromosome Location | Xq28 |
| Function | vasopressin receptor activity; |
| Pathway | Aquaporin-mediated transport, organism-specific biosystem; Arf6 trafficking events, organism-specific biosystem; Class A/1 (Rhodopsin-like receptors), organism-specific biosystem; G alpha (s) signalling events, organism-specific biosystem; GPCR downstream signaling, organism-specific biosystem; GPCR ligand binding, organism-specific biosystem; GPCRs, Class A Rhodopsin-like, organism-specific biosystem; |
| MIM | 300538 |
This gene encodes the vasopressin receptor, type 2, also known as the V2 receptor, which belongs to the seven-transmembrane-domain G protein-coupled receptor (GPCR) superfamily, and couples to Gs thus stimulating adenylate cyclase. The subfamily that includes the V2 receptor, the V1a and V1b vasopressin receptors, the oxytocin receptor, and isotocin and mesotocin receptors in non-mammals, is well conserved, though several members signal via other G proteins. All bind similar cyclic nonapeptide hormones. The V2 receptor is expressed in the kidney tubule, predominantly in the distal convoluted tubule and collecting ducts, where its primary property is to respond to the pituitary hormone arginine vasopressin (AVP) by stimulating mechanisms that concentrate the urine and maintain water homeostasis in the organism. When the function of this gene is lost, the disease Nephrogenic Diabetes Insipidus (NDI) results. The V2 receptor is also expressed outside the kidney although its tissue localization is uncertain. When these "extrarenal receptors" are stimulated by infusion of a V2 selective agonist (dDAVP), a variety of clotting factors are released into the bloodstream. The physiologic importance of this property is not known - its absence does not appear to be detrimental in NDI patients. The gene expression has also been described in fetal lung tissue and lung cancer associated with alternative splicing.
A: The SNAP tag (Single-stranded DNA binding protein) in the Human AVPR2-SNAP Stable Cell Line-HEK293 allows for the specific labeling of the AVPR2 receptor with fluorescent or biotinylated probes. This enables researchers to track the receptor's movement within the cell, study its subcellular localization, and investigate its trafficking pathways. The SNAP tag's unique ability to bind a wide range of probes without affecting the receptor's function makes it a valuable tool for cell biology studies.
A: The Human AVPR2-SNAP Stable Cell Line-HEK293 can be used in high-throughput screening assays to identify compounds that modulate AVPR2 activity. By measuring the effect of potential drugs on the receptor's function, researchers can identify lead compounds that may have antidiuretic properties. This cell line provides a reliable and reproducible model for assessing the efficacy and safety of new therapeutic agents targeting AVPR2.
A: The Human AVPR2-SNAP Stable Cell Line-HEK293 can serve as a model system to investigate the molecular defects leading to nephrogenic diabetes insipidus, a condition characterized by the inability to concentrate urine due to AVPR2 dysfunction. By studying the receptor's function in this cell line, researchers can gain insights into the underlying mechanisms of the disease and potentially identify novel therapeutic targets.
A: The Human AVPR2-SNAP Stable Cell Line-HEK293 can be used to study the effects of patient-specific genetic variations on AVPR2 function. By analyzing how these variations alter the receptor's activity, researchers can develop a better understanding of the molecular basis of individual responses to treatments. This knowledge can inform the design of personalized therapeutic strategies for disorders related to AVPR2, such as nephrogenic diabetes insipidus and hyponatremia.
A: The Human AVPR2-SNAP Stable Cell Line-HEK293 offers several advantages over primary cells for AVPR2 function studies. These include the ability to maintain consistent receptor expression levels, the capacity for large-scale production for high-throughput screening, and the reduced variability associated with primary cell cultures. Additionally, the HEK293 cell line is amenable to genetic manipulation, allowing for the creation of cell lines with specific genetic modifications that can be difficult to achieve in primary cells.
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