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SBDS Antikörper (N-Term)

Dieses Anti-SBDS-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von SBDS in WB und EIA. Geeignet für Human.
Produktnummer ABIN1449399

Kurzübersicht für SBDS Antikörper (N-Term) (ABIN1449399)

Target

Alle SBDS Antikörper anzeigen
SBDS (Shwachman-Bodian-Diamond Syndrome (SBDS))

Reaktivität

  • 35
  • 16
  • 16
  • 7
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
Human

Wirt

  • 34
  • 1
Maus

Klonalität

  • 31
  • 4
Monoklonal

Konjugat

  • 18
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser SBDS Antikörper ist unkonjugiert

Applikation

  • 17
  • 10
  • 8
  • 6
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)

Klon

AT1E8
  • Bindungsspezifität

    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 1-250, N-Term

    Kreuzreaktivität (Details)

    Species reactivity (tested):Human.

    Aufreinigung

    Protein-G affinity chromatography

    Immunogen

    Recombinant human SBDS (1-250aa) purified from E. coli

    Isotyp

    IgG2b
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1.0 mg/mL

    Buffer

    Phosphate -Buffered Saline ( pH 7.4) with 0.09 % Sodium Azide

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Handhabung

    Avoid repeated freezing and thawing.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    SBDS (Shwachman-Bodian-Diamond Syndrome (SBDS))

    Andere Bezeichnung

    SBDS

    Hintergrund

    The Shwachman-Bodian-Diamond syndrome (SBDS) is 249 amino acid ribosome maturation protein. The precise function of the SBDS protein is not known but it appears to play an important role in actin cytoskeletal function and mitotic spindle stabilization. Also, SBDS is required for the assembly of mature ribosomes and ribosome biogenesis. Mutations in the SBDS gene cause Shwachman-Diamond syndrome (SDS). SDS is an autosomal recessive disorder with clinical features that include pancreatic exocrine insufficiency, haematological dysfunction and skeletal abnormalities.Synonyms: Ribosome maturation protein SBDS, Shwachman-Bodian-Diamond syndrome protein

    Gen-ID

    51119

    NCBI Accession

    NP_057122

    UniProt

    Q9Y3A5

    Pathways

    Ribonucleoprotein Complex Subunit Organization, Ribosome Assembly
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