Recombinant Anti-DOPA Decarboxylase/DDC Antibody, Rabbit Monoclonal sinobiological 10560-R003

$1,900.00
In stock
SKU
10560-R003
Catalog No.SizePrice (USD)
10560-R003-11 mL$1,969.87
10560-R003-2020 µL$118.49
10560-R003-5050 µL$177.58
10560-R003-100100 µL$340.51

General Information

Product nameRecombinant Anti-DOPA Decarboxylase/DDC Antibody, Rabbit Monoclonal
Validated applicationsELISA(Cap) (FAQ Protocol)
Species reactivityReacts with: Human
SpecificityHuman DOPA Decarboxylase/DDC
ImmunogenRecombinant Human DOPA Decarboxylase / DDC Protein (Catalog#10560-H08B)
PreparationThis antibody was obtained from a rabbit immunized with purified, recombinant Human DOPA Decarboxylase / DDC (rh DOPA Decarboxylase / DDC; Catalog#10560-H08B; NP_000781.1; Met1-Glu480).
SourceMonoclonal Rabbit IgG Clone #003
PurificationProtein A
Formulation0.2 μm filtered solution in PBS
ConjugateUnconjugated
FormLiquid
ShippingThis antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
StorageThis 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.

Synonyms: Anti-AADC Antibody

Background Information

Full Namedopa decarboxylase (aromatic L-amino acid decarboxylase)
DescriptionDopa Decarboxylase (DDC), also known as AADC and Aromatic-L-amino acid decarboxylase, is a 54 kDa member of the group II decarboxylase family of proteins.It is a vitamin B6-dependent homodimeric enzyme that catalyzes the decarboxylation of both L-3,4-dihydroxyphenylalanine (L-DOPA) and L-5-hydroxytryptophan to dopamine and serotonin, respectively, which are major mammalian neurotransmitters and hormones belonging to catecholamines and indoleamines. Since L-DOPA is regularly used to treat the symptoms of Parkinson's disease, the catalytic pathway is of particular research interest. Defects of DDC are associated with severe developmental delay, oculogyric crises (OGC), as well as autosomal recessive disorder AADC deficiency, an early onset inborn error in neurotransmitter metabolism which can lead to catecholamine and serotonin deficiency.
Research Areas
  • Neurotransmitter Associated Enzymes
References
  1. Ichinose, H. et al.,1989,Biochem. Biophys. Res. Commun. 164: 1024-1030.
  2. Lisa, J. S. et al., 1992, Genomics 13: 469-471.
  3. Moore, P. S. et al.,1996, Biochem. J. 315:249-256.
  4. Bertoldi, M. et al., 2003, Biochim. Biophys. Acta. 1647:42-47.
  5. Vassilacopoulou, D. et al., 2004, Neurochem. Res. 29: 1817-1823.
  6. Ma, J.Z., et al., 2005, Hum. Mol. Genet. 14: 1691-1698.

title: Recombinant AAV vectors for treating neurodegenerative disorders
authors: Yezheng Tao; Shin-Shay Tian; Xiaoping Zhao
date: 2026-04-21
cited_by_count: 0
techniques: Blocking Assay; Construct; Control; Expressing; Transfection
bioz_score: 94

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