Tyrosine Hydroxylase Protein (TH) (Transcript Variant 2, Tyr3) (Myc-DYKDDDDK Tag)

N° du produit ABIN2712391

Détail du produit

Antigène: Tyrosine Hydroxylase (TH)

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 2, Tyr3

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette Tyrosine Hydroxylase protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human Tyrosine 3-monooxygenase (TH) (transcript variant 2) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

Antigène: Tyrosine Hydroxylase (TH)

Autre désignation: Tyrosine 3-Monooxygenase (Th) (TH Produits)

Synonymes: DYT14 Protein, DYT5b Protein, TYH Protein, The Protein, CG10118 Protein, DH65B Protein, DTH Protein, Dmel\\CG10118 Protein, Pale Protein, Ple Protein, TH Protein, Th Protein, VII Protein, dTH1 Protein, dTH65B Protein, pale/ple Protein, th Protein, dyt14 Protein, dyt5b Protein, tyh Protein, tyrosine hydroxylase Protein, pale Protein, tyrosine 3-monooxygenase Protein, tyrosine hydroxylase S homeolog Protein, TH Protein, Th Protein, ple Protein, th Protein, th.S Protein, LOC100008895 Protein

Sujet: The 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.

Poids moléculaire: 55.4 kDa

NCBI Accession: NP_000351

Pathways: Dopaminergic Neurogenesis, Response to Water Deprivation, Sensory Perception of Sound, Carbohydrate Homeostasis, Feeding Behaviour