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NSJ Bioreagents

SKU:F54418-0.08ML

AADC Antibody / DOPA Decarboxylase / DDC

AADC Antibody / DOPA Decarboxylase / DDC

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This 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.

Specifications

Family Primary antibody
Formulation In 1X PBS, pH 7.4, with 0.09% sodium azide
Format Purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit Ig
Species Reactivity Human, Mouse
Application FACS, IHC-P, WB, IF
Application Details Flow cytometry: 1:25 (1x10e6 cells),Immunohistochemistry (FFPE): 1:25,Western blot: 1:500-1:2000,Immunofluorescence: 1:25
Application Note The stated application concentrations are suggested starting points. Titration of the AADCantibody may be required due to differences in protocols and secondary/substrate sensitivity.
Localization Cytoplasmic
Immunogen A portion of amino acids 32-61 from the human protein was used as the immunogen for the AADC antibody.
Purity Antigen affinity purified
Storage Aliquot the AADC antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
Limitation This AADC antibody is available for research use only.
Uniprot # P20711
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/aadc-antibody-dopa-decarboxylase-ddc-f54418
Title AADC Antibody / DOPA Decarboxylase / DDC
Description This 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.
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