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PSPH Antikörper (N-Term)

Der Kaninchen Polyklonal Anti-PSPH-Antikörper wurde für WB validiert. Er ist geeignet, PSPH in Proben von Human und Maus zu detektieren. Es sind 3+ Publikationen verfügbar.
Produktnummer ABIN1881701

Kurzübersicht für PSPH Antikörper (N-Term) (ABIN1881701)

Target

Alle PSPH Antikörper anzeigen
PSPH (Phosphoserine Phosphatase (PSPH))

Reaktivität

  • 39
  • 16
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
Human, Maus

Wirt

  • 28
  • 11
  • 1
Kaninchen

Klonalität

  • 31
  • 9
Polyklonal

Konjugat

  • 30
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Dieser PSPH Antikörper ist unkonjugiert

Applikation

  • 33
  • 18
  • 12
  • 9
  • 7
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
Western Blotting (WB)

Klon

RB42215
  • Bindungsspezifität

    • 15
    • 8
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 7-36, N-Term

    Homologie

    Rat

    Aufreinigung

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This PSPH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 7-36 amino acids from the N-terminal region of human PSPH.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:1000. WB: 1:8000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Haltbarkeit

    6 months
  • Lamesch, Li, Milstein, Fan, Hao, Szabo, Hu, Venkatesan, Bethel, Martin, Rogers, Lawlor, McLaren, Dricot, Borick, Cusick, Vandenhaute, Dunham, Hill, Vidal: "hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes." in: Genomics, Vol. 89, Issue 3, pp. 307-15, (2007) (PubMed).

    Veiga-da-Cunha, Collet, Prieur, Jaeken, Peeraer, Rabbijns, Van Schaftingen: "Mutations responsible for 3-phosphoserine phosphatase deficiency." in: European journal of human genetics : EJHG, Vol. 12, Issue 2, pp. 163-6, (2004) (PubMed).

    Peeraer, Rabijns, Verboven, Collet, Van Schaftingen, De Ranter: "High-resolution structure of human phosphoserine phosphatase in open conformation." in: Acta crystallographica. Section D, Biological crystallography, Vol. 59, Issue Pt 6, pp. 971-7, (2003) (PubMed).

  • Target

    PSPH (Phosphoserine Phosphatase (PSPH))

    Andere Bezeichnung

    PSPH

    Hintergrund

    The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome.

    Molekulargewicht

    25008

    NCBI Accession

    NP_004568

    UniProt

    P78330

    Pathways

    Warburg Effekt
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