GPD1L Polyclonal Antibody (E-AB-52905)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human tonsil, Human liver cancer |
| Dilution | IHC 1:50-1:300 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Fusion protein of human GPD1L |
| Abbre | GPD1L |
| Synonyms | 2210409H23Rik, D9Ertd660e, GPD 1L, GPD1-L, GPD1L, Glycerol 3 phosphate dehydrogenase 1 like, Glycerol 3 phosphate dehydrogenase 1 like protein, Glycerol-3-phosphate dehydrogenase 1-like protein, KIAA0089, RGD1560123, gpd1l |
| Swissprot | |
| Cellular Localization | Cytoplasm. Localized to the region of the plasma membrane. |
| Concentration | 1.02 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Antigen affinity purification |
| Research Areas | Cancer, Cell Biology, Metabolism, Signal transduction |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| background | The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). |
Other Clones
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Other Formats
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Unconjugated
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