SKU: WR5242 Categories: ,

U-Blot® DDC Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR5242-100
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Product details

Background:dopa decarboxylase(DDC) Homo sapiens 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. [provided by RefSeq, Jun 2011],

Specifications

Size50μL/100μL
TargetDDC
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF, IP, ELISA
MW(Calculated)54kD
MW(Observed)54kD
Host SpeciesRabbit
IsotypeIgG,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:500-1:2000; WB 1:1000-1:20000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200; / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein A affinity chromatography.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRM1481R
ImmunogenThe specific immunogen used to produce this antibody is proprietary information.
SpecificityEndogenous
Gene NameDDC AADC
Protein NameAromatic-L-amino-acid decarboxylase (AADC) (DOPA decarboxylase) (DDC)
Other Name
SpeciesHuman
Gene ID1644
UniprotP20711,
Species.1Mouse
Gene ID.1
Uniprot.1O88533,
Species.2Rat
Gene ID.2
Uniprot.2P14173
Cellular Localizationcytosol,synaptic vesicle,axon,neuronal cell body,extracellular exosome,
Tissue Expression[Isoform 2]: High expression in kidney.
Signaling_pathwayOrganismal Systems >> Nervous system >> Dopaminergic synapse
Research Areas>>Tyrosine metabolism; / >>Phenylalanine metabolism; / >>Tryptophan metabolism; / >>Metabolic pathways; / >>Serotonergic synapse; / >>Dopaminergic synapse; / >>Cocaine addiction; / >>Amphetamine addiction; / >>Alcoholism
FunctionCatalytic activity:3,4-dihydroxy-L-phenylalanine = dopamine + CO(2).,Catalytic activity:5-hydroxy-L-tryptophan = 5-hydroxytryptamine + CO(2).,cofactor:Pyridoxal phosphate.,Disease:Defects in DDC are the cause of aromatic L-amino-acid decarboxylase deficiency (AADCD) [MIM:608643]. AADCD deficiency is an inborn error in neurotransmitter metabolism that leads to combined serotonin and catecholamine deficiency. It causes developmental and psychomotor delay, poor feeding, lethargy, ptosis, intermittent hypothermia, gastrointestinal disturbances. The onset is early in infancy and inheritance is autosomal recessive.,Function:Catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine, L-5-hydroxytryptophan to serotonin and L-tryptophan to tryptamine.,online information:Aromatic L-amino-acid decarboxylase entry,pathway:Catecholamine biosynthesis; dopamine biosynthesis; dopamine from L-tyrosine: step 2/2.,similarity:Belongs to the group II decarboxylase family.,subunit:Homodimer.,
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