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Read our guarantee »Products:Neuroscience >> Neurotransmitter >> Biogenic Amines >> Dopamine
Anti-DOPA Decarboxylase antibody [DDC-109]
See all DOPA Decarboxylase products (8) ...
Mouse monoclonal [DDC-109] to DOPA Decarboxylase
This antibody is specific to DOPA Decarboxylase
ICC/IF, WB, IP, Indirect ELISAmore details
Reacts with
Rat, Sheep, Rabbit, Guinea pig, Cow, Dog, Human, Monkey
Predicted to work with
Mouse, Pig, Zebrafish
A synthetic human DOPA Decarboxylase N terminal peptide (IEGRQVYPDVEPGYLR) corresponding to amino acids 24-39 conjugated to KLH.
IEGRQVYPDV EPGYLR
WB: Bovine brain extract ICC/IF: Brain tissue
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.
Preservative: 15mM Sodium Azide
Constituents: Ascites
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Ascites
In immunocytochemical labeling of brain tissue, the product stains the monoaminergic cells and proximal dendrites, but not cortical fibers.
Monoclonal
DDC-109
IgG2b
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Hormone biosynthesis
Neuroscience >> Neurotransmitter >> Biogenic Amines >> Dopamine
Our Abpromise guarantee covers the use of ab49916 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use at an assay dependent dilution.
WB: 1/1000Predicted molecular weight: 54 kDa.
IP: Use at an assay dependent dilution.
I-ELISA: Use at an assay dependent dilution.
Catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine, L-5-hydroxytryptophan to serotonin and L-tryptophan to tryptamine.
Catecholamine biosynthesis; dopamine biosynthesis; dopamine from L-tyrosine: step 2/2.
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.
Belongs to the group II decarboxylase family.
Target information above from: UniProt accessionP20711
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
ab49916 has not yet been referenced specifically in any publications.
Publishing research using ab49916? Please let us know so that we can cite the reference in this datasheet
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
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