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Anti tyrosine hydroxylase

Manufactured by Santa Cruz Biotechnology
Sourced in United States

Anti-tyrosine hydroxylase (TH) is a laboratory reagent used in research applications. Tyrosine hydroxylase is an enzyme that catalyzes the rate-limiting step in the biosynthesis of catecholamines, such as dopamine, norepinephrine, and epinephrine. Anti-TH antibodies are used to detect and quantify the presence of tyrosine hydroxylase in biological samples.

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3 protocols using anti tyrosine hydroxylase

1

Parkinsonian Mouse Model Protocols

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Methyl-4-phenylpyridine (MPP+; #D048), 1-methyl-4-phenyl-1,2,3,6-tetrahydro-pyridine (MPTP; #M0896) and levodopa (#D9628) were obtained from Sigma (St. Louis, MO, USA). An ABC reagent Box (Vector PK-6101 Rabbit IgG) and Golgi staining kit (PK401) were obtained from FD NeuroTechnologes (Columbia, MD, USA). P-tau (Ser396; #ab109390) and t-tau (#ab32057) were purchased from Abcam (Cambridge, MA), while GSK-3β (#12456) and phosphorylated GSK-3β (p-GSK-3β, ser9, #9323) were purchased from Cell Signaling Technology (Danvers, MA, USA). Anti-tyrosine hydroxylase (TH) was obtained from Santa Cruz (Dallas, TX, USA). Immoblilon PVDF membranes (#ISEQ00010) and Immobilon Western Chemiluminescent HRP Substrate (#WBKLS0100) were purchased from Merck Co. (Darmstadt, Germany).
SPF grade C57BL/6 mice, male 6–7 weeks, weight 22–27 g, were purchased from Guangdong Experimental Animal Center, license number: SYXK (Yue) 2016–0167, then free drinking water, feeding to 10–11 weeks. All of the experimental protocols were approved by the Institutional Animal Care and Use Committee of Southern Medical University (Guangzhou, Guangdong, China).
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2

Mitochondrial Dysfunction in Parkinson's Disease

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Materials used include: MPP+Iodide (Abcam), dimethyl fumarate (DMF) (Sigma Aldrich), JC-1 stain (Invitrogen, 3168), MTT (Invitrogen, M6494), DMSO (Sigma-Aldrich, D8418), Chemiluminescence western blotting substrate (Bio-Rad Laboratories, 1705061), Sucrose (Hi-media, MB025), OCT media (Sigma-Aldrich, SHH0026), T-PER extraction buffer (ThermoFisher, 78510), protease inhibitor (Sigma-Aldrich, P8340), Nitrocellulose membrane (GC-NCM-302), Bovine serum albumin (SRL, A6003), anti-Tyrosine Hydroxylase (TH) (Santa Cruz Biotechnology, sc25269), anti-α-synuclein (Santa Cruz Biotechnology, sc53955), anti-β-actin (Santa Cruz Biotechnology, sc47778), anti-NRF1 (Cell Signaling Technology, 12381S), anti-NRF2 (Sigma-Aldrich, SAB5700720), anti-PINK1 (Santa Cruz Biotechnology, sc517353), anti-Parkin (Santa Cruz Biotechnology, sc30130), LC-3A/B (Cell Signaling Technology, 12741S), anti-mouse Alexa flour 488 (A21202LC3), BECLIN-1 (3495S), BCL2 (NBP2-67182), anti-mouse secondary antibody (HRP-conjugated) (7076s), anti-rabbit secondary (HRP-conjugated) (AP307P), fluoroshield DAPI (F6057), Alexa fluor 488 Donkey Anti-Mouse IgG (H + L) (A-11008). All the chemicals used in the study were obtained from commercial vendors unless otherwise specified.
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3

Adrenergic Receptor Regulation in Cell Signaling

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Anti-tyrosine hydroxylase (TH) was purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Anti-β2-AR, anti-MMP2, anti-MMP9, anti-GAPDH (glyceraldehyde 3-phosphate dehydrogenase) antibodies, and β2-AR antagonist ICI118,551 were purchased from Abcam (Cambridge, UK). Anti-α1B-AR and anti-α2A-AR antibodies were purchased from Proteintech Group (Wuhan, China). Anti-Slug antibody was purchased from Cell Signaling Technology (Danvers, MA, USA). Anti-E-cadherin, anti-β1-AR, anti-vimentin antibodies, and rabbit IgG isotype control were purchased from GeneTex (San Antonio, TX, USA). Adrenergic receptor agonist NE was purchased from Aladdin (Shanghai, China). Nonselective α-AR blocker phentolamine hydrochloride was purchased from Sigma-Aldrich (Saint Louis, MO, USA).
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