HSD17B13 Polyclonal Antibody (E-AB-11308)
For research use only.
Verified Samples |
Verified Samples in IHC: Human ovarian cancer, Human colon cancer |
Dilution | IHC 1:50-1:200 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Rat |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Recombinant protein of human HSD17B13 |
Abbre | HSD17B13 |
Synonyms | 17-beta-HSD 13, 17-beta-hydroxysteroid dehydrogenase 13, DHB13, HMFN0376, Hsd17b13, SCDR9, Short-chain dehydrogenase/reductase 9, UNQ497/PRO1014 |
Swissprot | |
Cellular Localization | Secreted. |
Concentration | 0.5 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | 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 | Hydroxysteroid (17-beta) dehydrogenase 13, also designated Short-chain dehydrogenase/reductase 9 (SCDR9), which regulate the availability of steroids within various tissues throughout the body. HSD17B13 is a 300 amino acid secreted protein that is highly expressed in liver and is also detected in ovary, bone marrow, kidney, brain, lung, skeletal muscle, bladder and testis. The gene encoding HSD17B13 maps to chromosome 4, which houses nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. |
Other Clones
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Other Formats
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Unconjugated
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