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Tyrosine Hydroxylase Antikörper (pSer31)

Der Kaninchen Polyklonal Anti-Tyrosine Hydroxylase-Antikörper wurde für WB, IHC und IF validiert. Er ist geeignet, Tyrosine Hydroxylase in Proben von Ratte zu detektieren. Es sind 5+ Publikationen verfügbar.
Produktnummer ABIN361502

Kurzübersicht für Tyrosine Hydroxylase Antikörper (pSer31) (ABIN361502)

Target

Alle Tyrosine Hydroxylase (TH) Antikörper anzeigen
Tyrosine Hydroxylase (TH)

Reaktivität

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Ratte

Wirt

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Kaninchen

Klonalität

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  • 48
  • 1
Polyklonal

Konjugat

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Dieser Tyrosine Hydroxylase Antikörper ist unkonjugiert

Applikation

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Bindungsspezifität

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    pSer31

    Spezifität

    Specific for the ~60k tyrosine hydroxylase protein phosphorylated at Ser31.

    Kreuzreaktivität

    Maus, Ratte (Rattus)

    Homologie

    non-human primate

    Aufreinigung

    Antigen Affinity Purified from Pooled Serum

    Immunogen

    Synthetic phospho-peptide corresponding to amino acid residues surrounding Ser31 conjugated to KLH
  • Applikationshinweise

    Recommended Dilution: WB: 1:1000 IF (frozen sections, Witkovsky et al., 2000): 1:1000 IHC (frozen sections, Witkovsky et al., 2000): 1:1000 Quality Control: Western blots performed on each lot.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    100 μL in 10 mM HEPES (  pH 7.5), 150 mM NaCl, 100 μg per ml BSA and 50 % glycerol.

    Lagerung

    -20 °C
  • Calipari, Ferris, Melchior, Bermejo, Salahpour, Roberts, Jones: "Methylphenidate and cocaine self-administration produce distinct dopamine terminal alterations." in: Addiction biology, Vol. 19, Issue 2, pp. 145-55, (2014) (PubMed).

    Izumi, Ezumi, Takada-Takatori, Akaike, Kume: "Endogenous dopamine is involved in the herbicide paraquat-induced dopaminergic cell death." in: Toxicological sciences : an official journal of the Society of Toxicology, Vol. 139, Issue 2, pp. 466-78, (2014) (PubMed).

    Nakashima, Mori, Kaneko, Hayashi, Nagatsu, Ota: "Phosphorylation of the N-terminal portion of tyrosine hydroxylase triggers proteasomal digestion of the enzyme." in: Biochemical and biophysical research communications, Vol. 407, Issue 2, pp. 343-7, (2011) (PubMed).

    Jedynak, Ali, Haycock, Hope: "Acute administration of cocaine regulates the phosphorylation of serine-19, -31 and -40 in tyrosine hydroxylase." in: Journal of neurochemistry, Vol. 82, Issue 2, pp. 382-8, (2002) (PubMed).

    Salvatore, Waymire, Haycock: "Depolarization-stimulated catecholamine biosynthesis: involvement of protein kinases and tyrosine hydroxylase phosphorylation sites in situ." in: Journal of neurochemistry, Vol. 79, Issue 2, pp. 349-60, (2001) (PubMed).

  • Target

    Tyrosine Hydroxylase (TH)

    Andere Bezeichnung

    Tyrosine Hydroxylase

    Hintergrund

    Tyrosine hydroxylase (TH) is the rate-limiting enzyme in the synthesis of the catecholamines dopamine and norepinephrine. TH antibodies can therefore be used as markers for dopaminergic and noradrenergic neurons in a variety of applications including depression, schizophrenia, Parkinson’s disease and drug abuse (Kish et al., 2001, Zhu et al., 2000, Zhu et al., 1999). TH antibodies can also be used to explore basic mechanisms of dopamine and norepinephrine signaling (Witkovsky et al., 2000, Salvatore et al., 2001, Dunkley et al., 2004). The activity of TH is also regulated by phosphorylation (Haycock et al., 1982, Haycock et al., 1992, Jedynak et al., 2002). Phospho-specific antibodies for the phosphorylation sites on TH can be used to great effect in studying this regulation and in identifying the cells in which TH phosphorylation occurs. Anti-Phospho Ser31 Tyrosine Hydroxylase Western blot of PC-12 cells incubated in the absence (Control) and presence of okadaic acid (OA, 1 µM for 60 min) showing specific immunolabeling of the ~60k TH phosphorylated at Ser31.

    Molekulargewicht

    '60 kDa

    Gen-ID

    25085

    UniProt

    P04177

    Pathways

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