SLC20A2 - Sodium-dependent phosphate transporter 2
Order number: 71771
Description
We are excited to introduce our off-the-shelf, full-length, active, and native Sodium-dependent phosphate transporter 2, commonly known as SLC20A2. SLC20A2
is primarily responsible for maintaining cellular phosphate homeostasis by transporting inorganic phosphate across plasma membranes.
Dysfunctional mutations in this gene are a leading cause of Primary Familial Brain Calcification, as impaired phosphate transport leads to calcium phosphate deposits in the basal ganglia and other brain regions.
Our SLC20A2 protein has been solubilized and stabilized using our NativeMP™ platform, ensuring it retains its native structure and full biological activity, making it ideal for various research applications.
Our SLC20A2 protein has been solubilized and stabilized using our NativeMP™ platform, ensuring it retains its native structure and full biological activity, making it ideal for various research applications.
Applications:
- Screening/Validation
- Biologics Development
- Structure Determination
- Small Molecule Drug Development
The protein delivered can be used for these specific applications. When ordering, please indicate which applications you intend to use the protein for in the contact form to ensure the best results.
For more details, explore our solubilization database.

Datasheets
Upon ordering, you will receive the corresponding datasheets and the Certificate of Analysis (CoA).
| Feature | |
|---|---|
| Alternative names | PIT2, GLVR2, Gibbon ape leukemia virus receptor 2, Phosphate transporter 2 |
| UniProt Number | Q08357 |
| Protein class | SLC transporter |
| Original host | Homo sapiens |
| Expression system | HEK293 |
| Sequence, One-Letter Code | MAMDEYLWMVILGFIIAFILAFSVGANDVANSFGTAVGSGVVTLRQACILASIFETTGSVLLGAKVGETIRKGIIDVNLYNETVETLMAGEVSAMVGSAVWQLIASFLRLPISGTHCIVGSTIGFSLVAIGTKGVQWMELVKIVASWFISPLLSGFMSGLLFVLIRIFILKKEDPVPNGLRALPVFYAATIAINVFSIMYTGAPVLGLVLPMWAIALISFGVALLFAFFVWLFVCPWMRRKITGKLQKEGALSRVSDESLSKVQEAESPVFKELPGAKANDDSTIPLTGAAGETLGTSEGTSAGSHPRAAYGRALSMTHGSVKSPISNGTFGFDGHTRSDGHVYHTVHKDSGLYKDLLHKIHIDRGPEEKPAQESNYRLLRRNNSYTCYTAAICGLPVHATFRAADSSAPEDSEKLVGDTVSYSKKRLRYDSYSSYCNAVAEAEIEAEEGGVEMKLASELADPDQPREDPAEEEKEEKDAPEVHLLFHFLQVLTACFGSFAHGGNDVSNAIGPLVALWLIYKQGGVTQEAATPVWLLFYGGVGICTGLWVWGRRVIQTMGKDLTPITPSSGFTIELASAFTVVIASNIGLPVSTTHCKVGSVVAVGWIRSRKAVDWRLFRNIFVAWFVTVPVAGLFSAAVMALLMYGILPYVGSSGTETSQVAPA |
| Affinity tags | Rho1D4-tag (C-terminal) |
| Size (excluding additional elements) | 665 amino acids, 72 kDa |
| Concentration | 0.4 - 0.7 mg/mL |
| Purity | >90%, determined via SDS-PAGE |
| Purification process | 2-step purification |
| Shipping | Shipment is carried out on dry-ice for temperature stability to ensure the integrity of the product. |
| Function | The solute carrier family 20 member 2 is a sodium-dependent inorganic phosphate cotransporter that plays a critical role in maintaining cellular phosphate homeostasis by mediating the transport of Pi across plasma membranes. It is also essential for the regulation of mineral deposition in the brain, a process that involves preventing the pathological accumulation of calcium phosphate in the vascular extracellular matrix. Mutations in this gene have been linked to primary familial brain calcification, a neurodegenerative condition characterized by bilateral deposits in the basal ganglia and other cerebral regions. |
| PubMed ID | 39121859, 38195526, 35881308, 25726928 |