Key features and details
- Rabbit polyclonal to Tyrosine Hydroxylase - Neuronal Marker
- Suitable for: IHC-P, ICC/IF, WB
- Reacts with: Mouse, Rat, Cat, Human
- Isotype: IgG
製品名Anti-Tyrosine Hydroxylase antibody - Neuronal Marker
Tyrosine Hydroxylase 一次抗体 製品一覧
製品の詳細Rabbit polyclonal to Tyrosine Hydroxylase - Neuronal Marker
アプリケーション適用あり: IHC-P, ICC/IF, WBmore details
種交差性交差種: Mouse, Rat, Cat, Human
Full length SDS denatured protein (purified from pheochromocytoma) (Rat).
ab112 can be used as a marker for dopaminergic and noradrenergic neurons.
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保存方法Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
Constituents: 0.01% BSA, 0.87% Sodium chloride, 50% Glycerol, 0.238% HEPES
Concentration information loading...
精製度Protein A purified
Our Abpromise guarantee covers the use of ab112 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/200. Predicted molecular weight: 60 kDa.|
機能Plays an important role in the physiology of adrenergic neurons.
組織特異性Mainly expressed in the brain and adrenal glands.
パスウェイCatecholamine biosynthesis; dopamine biosynthesis; dopamine from L-tyrosine: step 1/2.
関連疾患Defects in TH are the cause of dystonia DOPA-responsive autosomal recessive (ARDRD) [MIM:605407]; also known as autosomal recessive Segawa syndrome. ARDRD is a form of DOPA-responsive dystonia presenting in infancy or early childhood. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. Some cases of ARDRD present with parkinsonian symptoms in infancy. Unlike all other forms of dystonia, it is an eminently treatable condition, due to a favorable response to L-DOPA.
Note=May play a role in the pathogenesis of Parkinson disease (PD). A genome-wide copy number variation analysis has identified a 34 kilobase deletion over the TH gene in a PD patient but not in any controls.
配列類似性Belongs to the biopterin-dependent aromatic amino acid hydroxylase family.
- Information by UniProt
- Dystonia 14 antibody
- DYT14 antibody
- DYT5b antibody
ab112 staining Tyrosine Hydroxylase in mouse brain tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections).
Tissue was fixed with formaldehyde and blocked with 1% BSA for 10 minutes at 21°C; antigen retrieval was by heat mediation in citric acid. Samples were incubated with primary antibody (1/800 in TBS/BSA/azide) for 2 hours at 21°C. A Biotin-conjugated goat anti-rabbit IgG polyclonal (1/250) was used as the secondary antibody.
The image of Caudate putamen shows characteristic nerve fibre positivity
Anti-Tyrosine Hydroxylase antibody - Neuronal Marker (ab112) at 1/200 dilution + PC-12 (Rat adrenal gland pheochromocytoma cell line) whole cell lysate
Predicted band size: 60 kDa
Paraffin embedded sections of rat brain tissue were stained for Tyrosine Hydroxylase with ab112 at 1/5000 dilution in immunohistochemical analysis (Panel 1).
Panel 2 shows an image in which ab112 was replaced with a Rabbit IgG1 isotype control.
Effects of hypercholesterolemia on tyrosine hydroxylase (TH)-immunoreactivity in striatum (NCP) and TH-positive nigral (SN) neurons in MPTP-treated mice.
Representative NCP (A-D) and SN (E-H) photographs from CS, HCD, MPTP and HCD+MPTP (left to right) groups showing TH-immunoreactivity.
Mice were anesthetized with chloral hydrate (350 mg/kg; i.p.) and perfused intracardially with phosphate buffered saline (PBS, 0.1 M; pH 7.4) followed by 4% w/v PFA in PBS. Brains were removed and kept overnight in the same fixative, transferred to 30% w/v sucrose solution. 20 μm thick coronal sections passing through the NCP and SN were taken using Cryotome in poly-L-lysine coated slides. The sections were rinsed three times with 0.1 M Tris-buffered saline (TBS, 0.1 M; pH 7.4), incubated in 3% H2O2 in TBS, permeabilized with 0.3% Triton X-100, and blocked with 10% donkey serum containing 0.3% Triton X-100. The sections were incubated overnight with primary antibody for TH ab112 (1:700) in TBS, containing 2% donkey serum at 4°C and then incubated with HRP-conjugated secondary antibody (1:1000) in TBS for 1 h at room temperature. Colour development was performed by incubating the sections in DAB-liquid substrate system and then sections were washed, dehydrated, cleared in xylene, mounted in DPX and photographed under bright field illumination using a digital SLR camera.
Lateral localization of CB1-R-dense striosome-dendron bouquets and ventral tier SNpc enveloping CB1-R-immunoreactive axons through the substantia nigra (mouse).
An example of a TH- and CB1-R-positive dendron in the rostral SN is shown in Panel C.
Coronal vibratome sections (40 μm) or glycerol cryoprotected frozen sliding microtome sections (30 μm) were taken at levels extending from the prefrontal cortex to the ventral mesencephalon, and every 3rd to 6th section, depending on the experiment, was stained and imaged. Sections were washed in PBS-T (0.2% Triton X-100), blocked for 4 hours with 5% BSA in PBST, and incubated in primary antibodies overnight to 48 hours in a cold room on an orbital shaker.
ab112 staining tyrosine hydroxulase in mouse brain tissue.
Sections were permeabilized with 0.5% Triton X-100 in PBS at room temperature for 10 minutes. Samples were incubated with primary antibody (1:500) overnight at 4C.
PFA-fixed, Triton X-100 permeabilized human neurons in cerebral organoid stained for Tyrosine Hydroxylase (green) using ab112 at 1/300 dilution in ICC/IF.
All lanes : Anti-Tyrosine Hydroxylase antibody - Neuronal Marker (ab112) at 1/200 dilution
All lanes : Mouse cell lysate (CATH.a neuron)
Lysates/proteins at 40 µg per lane.
All lanes : Goat Anti-Rabbit HRP
Developed using the ECL technique.
Predicted band size: 60 kDa
Exposure time: 50 seconds
ab112 at 1/800 staining rat dopaminergic neuronal tissue sections (araldite resin sections) by immunohistochemistry.
The tissue was paraformaldehyde fixed and then an antigen retrieval step was carried out (heat mediated). A biotinylated goat anti-rabbit IgG (ab6720) was used as the secondary.
Anti-Tyrosine Hydroxylase antibody - Neuronal Marker (ab112) at 1/200 dilution + rat caudate lysate at 10 µg
Predicted band size: 60 kDa
ab112 は 166 報の論文で使用されています。
- Nullmeier S et al. Glutamic acid decarboxylase 67 haplodeficiency in mice: consequences of postweaning social isolation on behavior and changes in brain neurochemical systems. Brain Struct Funct 225:1719-1742 (2020). PubMed: 32514634
- Zhou L et al. Colocalization of dopamine receptors in BDNF-expressing peptidergic neurons in the paraventricular nucleus of rats. J Chem Neuroanat 106:101794 (2020). PubMed: 32315740
- You MJ et al. Human umbilical cord-derived mesenchymal stem cells alleviate schizophrenia-relevant behaviors in amphetamine-sensitized mice by inhibiting neuroinflammation. Transl Psychiatry 10:123 (2020). PubMed: 32341334
- Koga K et al. Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex. Mol Brain 13:49 (2020). PubMed: 32216807
- Cao S et al. Fast Localization and Sectioning of Mouse Locus Coeruleus. Biomed Res Int 2020:4860735 (2020). PubMed: 32190666