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TBL2 Antikörper (N-Term)

Dieses Anti-TBL2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von TBL2 in WB und IHC (p). Geeignet für Human.
Produktnummer ABIN2845981

Kurzübersicht für TBL2 Antikörper (N-Term) (ABIN2845981)

Target

Alle TBL2 Antikörper anzeigen
TBL2 (Transducin (Beta)-Like 2 (TBL2))

Reaktivität

  • 23
  • 4
  • 2
  • 2
  • 2
Human

Wirt

  • 21
  • 2
Kaninchen

Klonalität

  • 23
Polyklonal

Konjugat

  • 18
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser TBL2 Antikörper ist unkonjugiert

Applikation

  • 22
  • 11
  • 11
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Klon

RB32541
  • Bindungsspezifität

    • 8
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 43-72, N-Term

    Aufreinigung

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

    Immunogen

    This TBL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 43-72 amino acids from the N-terminal region of human TBL2.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:1000. IHC-P: 1:10~50

    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

    Informationen zur Lagerung

    TBL2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Haltbarkeit

    6 months
  • Target

    TBL2 (Transducin (Beta)-Like 2 (TBL2))

    Andere Bezeichnung

    TBL2

    Hintergrund

    This gene encodes a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.

    Molekulargewicht

    49798

    Gen-ID

    26608

    NCBI Accession

    NP_036585

    UniProt

    Q9Y4P3
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