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Goat Anti-Tyrosine Hydroxylase Antibody

Peptide-affinity purified goat antibody

  • WB - Goat Anti-Tyrosine Hydroxylase Antibody AF2127a
    AF2127a (2 µg/ml) staining of Human Cerebral Cortex lysate (35 µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession P07101
Other Accession NP_954987, 7054
Reactivity Human
Predicted Rat, Dog
Host Goat
Clonality Polyclonal
Concentration 100ug/200ul
Isotype IgG
Calculated MW 58600 Da
Additional Information
Gene ID 7054
Other Names Tyrosine 3-monooxygenase,, Tyrosine 3-hydroxylase, TH, TH, TYH
Format 0.5 mg IgG/ml in Tris saline (20mM Tris pH7.3, 150mM NaCl), 0.02% sodium azide, with 0.5% bovine serum albumin
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsGoat Anti-Tyrosine Hydroxylase Antibody is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name TH
Synonyms TYH
Function Plays an important role in the physiology of adrenergic neurons.
Tissue Location Mainly expressed in the brain and adrenal glands
Research Areas
Citations (0)

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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.


[Genetic polymorphism in tyrosine hydroxylase gene and essential hypertension in Hunan Han population.] Chen L, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban, 2010 Aug. PMID 20818075.
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease. Bademci G, et al. Hum Mutat, 2010 Aug 31. PMID 20809526.
Tyrosine Hydroxylase Polymorphism (C-824T) and Hypertension: A Population-Based Study. Nielsen SJ, et al. Am J Hypertens, 2010 Aug 12. PMID 20706199.
[Study of follicle-stimulating hormone receptor and tyrosine hydroxylase polymorphisms and pre-eclampsia in Chinese Han population] Chen Y, et al. Zhonghua Yi Xue Za Zhi, 2010 May 4. PMID 20646572.
Variation at the NFATC2 Locus Increases the Risk of Thiazolinedinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study. Bailey SD, et al. Diabetes Care, 2010 Jul 13. PMID 20628086.

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$ 325.00
Cat# AF2127a
(40 western blots)
Availability: 7-10 days
Bulk Size
Seasonal Special on Bulk Order
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