Tyrosine Hydroxylase (TH) Mouse Monoclonal Antibody [Kloon ID: LBI1A12]

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. [provided by RefSeq, Jul 2008]

Carrier-free (BSA/glycerol-free) TH mouse monoclonal antibody, clone LBI1A12

DYT5b; DYT14; TYH

Homo sapiens tyrosine hydroxylase (TH), transcript variant 2, mRNA.

7054

P07101

Unconjugated

Metabolic pathways, Parkinson's disease, Tyrosine metabolism

Metabolic pathways, Parkinson's disease, Tyrosine metabolism

WB 1:4000, IF 1:100, IHC: 1:150

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

TH

https://www.ncbi.nlm.nih.gov/gene/?term=7054

https://www.uniprot.org/uniprot/P07101