Tyrosine Hydroxylase rabbit pAb

Tyrosine Hydroxylase rabbit pAb

AO-06-ES8886-100

Tyrosine Hydroxylase rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES8886
Product nameTyrosine Hydroxylase rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameTyrosine 3-monooxygenase (EC 1.14.16.2) (Tyrosine 3-hydroxylase) (TH)
Size100μL
Unit price ($)248
Human gene ID7054
Human Swiss-ProtP07101
SourceRabbit
IsotypeIgG
TargetTyrosine Hydroxylase
Fields>>Tyrosine metabolism;>>Folate biosynthesis;>>Metabolic pathways;>>Dopaminergic synapse;>>Prolactin signaling pathway;>>Parkinson disease;>>Cocaine addiction;>>Amphetamine addiction;>>Alcoholism
Gene nameTH TYH
Protein nameTyrosine 3-monooxygenase (EC 1.14.16.2) (Tyrosine 3-hydroxylase) (TH),Tyrosine Hydrolase
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID21823
Mouse gene link
Mouse Swiss-ProtP24529
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID25085
Rat gene link
Rat Swiss-ProtP04177
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human Tyrosine Hydroxylase Polyclonal
SpecificityThis antibody detects endogenous levels of Tyrosine Hydroxylase.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000, ELISA 1:10000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)60kD
BackgroundThe protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate-limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008],
Functioncatalytic activity:L-tyrosine + tetrahydrobiopterin + O(2) = 3,4-dihydroxy-L-phenylalanine + 4a-hydroxytetrahydrobiopterin.,cofactor:Fe(2+) ion.,disease:Defects in TH are the cause of dystonia DOPA-responsive autosomal recessive (ARDRD) [MIM:605407]; also known as autosomal recessive Segawa syndrome. ARDRD is a form of DOPA-responsive dystonia presenting in infancy or early childhood. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. Some cases of ARDRD present with parkinsonian symptoms in infancy. Unlike all other forms of dystonia, it is an eminently treatable condition, due to a favorable response to L-DOPA.,enzyme regulation:Phosphorylation leads to an increase in the catalytic activity.,function:Plays an important role in the physiology of adrenergic neurons.,online information:Tyrosine hydroxylase entry,pathway:Ca
Subcellular locationCytoplasm, perinuclear region . Nucleus . Cell projection, axon . Cytoplasm . Cytoplasmic vesicle, secretory vesicle, synaptic vesicle . When phosphorylated at Ser-19 shows a nuclear distribution and when phosphorylated at Ser-31 as well at Ser-40 shows a cytosolic distribution (By similarity). Expressed in dopaminergic axons and axon terminals. .
ExpressionMainly expressed in the brain and adrenal glands.

Additional Images

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Western blot analysis of various lysate, antibody was diluted at 1000. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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: AO-06-ES8886-100
: 10 Items
Hurry! only 10 items left in stock.

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