Recombinant DOPA Decarboxylase/DDC Monoclonal Antibody (AN300344P)
For research use only.
| Verified Samples | Verified Samples in IHC: Human brain |
| Dilution | IHC-P 1:100-1:500 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | IHC-P |
| Clonality | Monoclonal |
| Immunogen | Recombinant Human DOPA Decarboxylase/DDC protein |
| Abbre | DDC |
| Synonyms | DDC, AADC, Aromatic L Amino Acid Decarboxylase, Aromatic-L-amino-acid decarboxylase, DDC_HUMAN, DOPA decarboxylase, DOPA decarboxylase (aromatic L-amino acid decarboxylase) |
| Swissprot | |
| Concentration | 1 mg/mL |
| Buffer | 0.2 μm filtered solution in PBS |
| Purification Method | Protein A |
| Research Areas | Neuroscience, Cancer, Metabolism |
| Clone No. | 6A1 |
| Conjugation | Unconjugated |
| Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
| Shipping | Ice bag |
| background | The encoded protein catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine, L-5-hydroxytryptophan to serotonin and L-tryptophan to tryptamine. Defects in this gene are the cause of aromatic L-amino-acid decarboxylase deficiency (AADCD). AADCD deficiency is an inborn error in neurotransmitter metabolism that leads to combined serotonin and catecholamine deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. |
Other Clones
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Other Formats
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Unconjugated
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