PDSS2 Polyclonal Antibody (E-AB-16698)

For research use only.
Verified Samples |
Verified Samples in WB: Hela Verified Samples in IHC: Human liver cancer |
Dilution | WB 1:500-1:2000, IHC 1:25-1:100 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human |
Applications | WB, IHC |
Clonality | Polyclonal |
Immunogen | Synthetic peptide of human PDSS2 |
Abbre | PDSS2 |
Synonyms | All-trans-decaprenyl-diphosphate synthase subunit 2, C6orf210, Candidate tumor suppressor protein, Decaprenyl pyrophosphate synthase subunit 2, Decaprenyl-diphosphate s, bA59I9.3, chromosome 6 open reading frame 210, decaprenyl pyrophosphate synthetase subunit 2 |
Swissprot | |
Calculated MW | 44 kDa |
Cellular Localization | Mitochondrion. |
Concentration | 0.3 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Cancer, 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 is an enzyme that synthesizes the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. The gene product catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. Defects in this gene are a cause of coenzyme Q10 deficiency. |
Other Clones
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Other Formats
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Unconjugated
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