DOPA Decarboxylase (2C12) Monoclonal Antibody

$Paraformaldehyde-fixed and paraffin-embedded Human Kidney tissue incubated DOPA Decarboxylase (2C12) Monoclonal Antibody (bsm-54061R) at 1:100, overnight at 4\u00b0C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.$

Paraformaldehyde-fixed and paraffin-embedded Human Kidney tissue incubated DOPA Decarboxylase (2C12) Monoclonal Antibody (bsm-54061R) at 1:100, overnight at 4\u00b0C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.

$Paraformaldehyde-fixed and paraffin-embedded Human Liver tissue incubated DOPA Decarboxylase (2C12) Monoclonal Antibody (bsm-54061R) at 1:100, overnight at 4\u00b0C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.$

Paraformaldehyde-fixed and paraffin-embedded Human Liver tissue incubated DOPA Decarboxylase (2C12) Monoclonal Antibody (bsm-54061R) at 1:100, overnight at 4\u00b0C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.

Applications

WB
IHC-P

Reactivity

Human
Mouse
Rat

Overview
Catalog #	bsm-54061R
Product Name	DOPA Decarboxylase (2C12) Monoclonal Antibody
Applications	WB, IHC-P
Reactivity	Human, Mouse, Rat
Specifications
Conjugation	Unconjugated
Host	Rabbit
Source	N terminal human DOPA Decarboxylase
Clonality	Monoclonal
Clone #	2C12
Isotype	IgG
Concentration	1ug/ul
Purification	Purified by Protein A.
Storage Buffer	Aqueous buffered solution containing 1xTBS (pH7.4), 1%BSA, 40%Glycerol and 0.05% Sodium Azide.
Storage Condition	Store at 4C for up to 2 weeks. For long term storage, store at -20C in small aliquots to prevent freeze-thaw cycles.
Target
Gene ID	1644
Swiss Prot	P20711
Synonyms	Aromatic-L-amino-acid decarboxylase, DOPA decarboxylase, AADC, DDC
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.
Application Dilution
WB	1:300-5000
IHC-P	1:200-400

Applications

Reactivity

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