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Ubiquitin hydrolase 1 Antikörper

Der Maus Monoklonal anti-Ubiquitin hydrolase 1 Antikörper wird verwendet zum Nachweis von Ubiquitin hydrolase 1 in Proben von Human, Rind (Kuh), Maus und Ratte. Er wurde validiert für WB und IHC.
Produktnummer ABIN5688748
792,00 €
Zzgl. Versandkosten 20,00 € und MwSt
0.1 mL
Lieferung nach: Deutschland
Lieferung in 6 bis 8 Werktagen

Kurzübersicht für Ubiquitin hydrolase 1 Antikörper (ABIN5688748)

Target

Ubiquitin hydrolase 1

Reaktivität

Human, Rind (Kuh), Maus, Ratte

Wirt

  • 1
  • 1
Maus

Klonalität

  • 1
  • 1
Monoklonal

Konjugat

  • 2
Unkonjugiert

Applikation

  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)

Klon

MCA-BH7
  • Spezifität

    Specific for the ~24  kDa UCHL1 protein.

    Aufreinigung

    Total IgG fraction

    Immunogen

    Recombinant full length human UCHL1 purified from E. coli.

    Isotyp

    IgG1
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Ubiquitin Hydrolase 1 antibody can be stored at -20°C and is stable at -20°C for at least 1 year.
  • Target

    Ubiquitin hydrolase 1

    Hintergrund

    Ubiquitin C-terminal hydrolase 1 (UCHL1) is also known as ubiquitin carboxyl esterase L1, ubiquitin thiolesterase, neuron-specific protein PGP9.5 and Park5. It was originally identified as a major component of the neuronal cytoplasm from 2-dimensional gel analysis of brain tissues, and was given the name PGP9.5. It was later found that ubiquitin C-terminal hydrolase enzyme activity was associated with the PGP9.5 protein. The ubiquitin C-terminal hydrolases cleave ubiquitin from other molecules. Regulation of the ubiquitin pathway is very important and many disease states are associated with defects in this pathway. Genetic knockout of UCHL1 in mice results in a motor neuron degeneration similar to the spontaneous gracile axonal dystrophy (gad) mutant mice. Point mutations in the UCHL1 gene are associated with some forms of human Parkinson's disease. Since UCHL1 is heavily expressed in neurons, it is released in large amounts following injury or degeneration, so the detection of UCHL1 in CSF and other bodily fluids can be used as a biomarker.

    Molekulargewicht

    24 kDa

    Gen-ID

    7345

    UniProt

    P09936
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