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HEPACAM2 Antikörper (AA 31-345)

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch HEPACAM2 in ELISA, WB und IHC (p). Es zeigt Reaktivität gegenüber Proben von Human.
Produktnummer ABIN7873784
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für HEPACAM2 Antikörper (AA 31-345) (ABIN7873784)

Target

Alle HEPACAM2 Antikörper anzeigen
HEPACAM2 (HEPACAM Family Member 2 (HEPACAM2))

Reaktivität

  • 22
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 22
Kaninchen

Klonalität

  • 22
Polyklonal

Konjugat

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
Dieser HEPACAM2 Antikörper ist unkonjugiert

Applikation

  • 16
  • 13
  • 3
  • 2
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Bindungsspezifität

    • 8
    • 5
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 31-345

    Verwendungszweck

    HEPACAM2 Antibody / HEPACAM family member 2

    Aufreinigung

    Antigen affinity chromatography

    Immunogen

    An E.coli-derived human recombinant protein (amino acids G31-K345) was used as the immunogen for the HEPACAM2 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the HEPACAM2 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    After reconstitution, the HEPACAM2 Antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    HEPACAM2 (HEPACAM Family Member 2 (HEPACAM2))

    Andere Bezeichnung

    HEPACAM2

    Hintergrund

    HEPACAM family member 2 is a protein that in humans is encoded by the HEPACAM2 gene. This gene encodes a protein related to the immunoglobulin superfamily that plays a role in mitosis. Knockdown of this gene results in prometaphase arrest, abnormal nuclear morphology and apoptosis. Poly(ADP-ribosylation) of the encoded protein promotes its translocation to centrosomes, which may stimulate centrosome maturation. A chromosomal deletion including this gene may be associated with myeloid leukemia and myelodysplastic syndrome in human patients.

    UniProt

    A8MVW5
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