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UFD1L Antikörper (AA 1-277)

Dieses Anti-UFD1L-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von UFD1L in WB, IHC und IF. Geeignet für Human.
Produktnummer ABIN1885878

Kurzübersicht für UFD1L Antikörper (AA 1-277) (ABIN1885878)

Target

Alle UFD1L Antikörper anzeigen
UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))

Reaktivität

  • 41
  • 27
  • 26
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 35
  • 5
Kaninchen

Klonalität

  • 34
  • 7
Polyklonal

Konjugat

  • 26
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser UFD1L Antikörper ist unkonjugiert

Applikation

  • 38
  • 13
  • 10
  • 10
  • 7
  • 6
  • 6
  • 5
  • 3
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Bindungsspezifität

    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-277

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 277 of UFD1L
  • Applikationshinweise

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.500
    Immunofluorescence: 1.100-1.200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))

    Andere Bezeichnung

    UFD1L

    Hintergrund

    The protein encoded by this gene forms a complex with two other proteins, NPL4 and VCP, that is necessary for the degradation of ubiquitinated proteins.In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis.Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects.Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq]

    Molekulargewicht

    35 kDa

    Gen-ID

    7353

    NCBI Accession

    NP_005650, NM_005659
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