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SAB2501155

Sigma-Aldrich

Anti-Tyrosine Hydroxylase Antibody

goat polyclonal

Sinónimos:

Anti-TYH, tyrosine hydroxylase

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

Nombre del producto

Anti-TH (C-terminal) antibody produced in goat, affinity isolated antibody, buffered aqueous solution

origen biológico

goat

Nivel de calidad

conjugado

unconjugated

forma del anticuerpo

affinity isolated antibody

tipo de anticuerpo

primary antibodies

clon

polyclonal

Formulario

buffered aqueous solution

reactividad de especies

rat, canine, human

técnicas

ELISA: suitable
immunohistochemistry: suitable
western blot: suitable

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

unmodified

Información sobre el gen

human ... TH(7054)

Categorías relacionadas

Descripción general

Tyrosine hydroxylase (TH) is encoded by the gene mapped to human chromosome 11p15.5. The N-terminal end of the protein plays a vital role in maintaining intracellular stability of the enzyme. Tyrosine hydroxylase is expressed in various tissues such as brain, adrenal medulla, and sympathetically innervated tissues. The enzyme is characterized with a regulatory domain (R), a catalytic domain (C) at N-terminal end, and a coiled-coil domain at the C-terminal end.

Inmunógeno

Peptide with sequence CVQDELDTLAHAL, from the C Terminus of the protein sequence according to NP_954986.2; NP_000351.2; NP_954987.2.

Acciones bioquímicas o fisiológicas

Tyrosine hydroxylase (TH) specifically catalyzes the hydroxylation of the amino acid L-tyrosine to 3, 4-dihydroxy-L-phenylalanine (L-DOPA). TH is a rate-limiting enzyme involved in the synthesis of catecholamine, which is involved in several brain functions, such as attention, memory, cognition, and emotion. Phosphorylation of the N-terminal portion of tyrosine hydroxylase controls the degradation of this enzyme by the ubiquitin-proteasome pathway. Alteration in the expression of the gene results in the pathogenesis of Parkinson′s disease (PD) and point mutation in the gene coding for TH leads to Segawa′s syndrome.

Características y beneficios

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Forma física

Supplied at 0.5 mg/mL in Tris saline with 0.02% sodium azide and 0.5% bovine serum albumin.

Cláusula de descargo de responsabilidad

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Visite la Librería de documentos

A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome.
Ludecke B
Human Gene Therapy (1995)
Human tyrosine hydroxylase and insulin genes are contiguous on chromosome 11.
O'Malley KL and Rotwein P
Nucleic Acids Research (1988)
The function of tyrosine hydroxylase in the normal and Parkinsonian brain.
CNS & Neurological Disorders Drug Targets (2012)
Phosphorylation of the N-terminal portion of tyrosine hydroxylase triggers proteasomal digestion of the enzyme.
Nakashima A
Biochemical and Biophysical Research Communications (2011)
Tyrosine hydroxylase and regulation of dopamine synthesis.
Archives of Biochemistry and Biophysics (2011)

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