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ENTHD1 Antikörper (Biotin)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch ENTHD1 in WB und IHC (p). Er zeigt eine Reaktivität gegenüber Human, Maus und Ratte.
Produktnummer ABIN1402993

Kurzübersicht für ENTHD1 Antikörper (Biotin) (ABIN1402993)

Target

ENTHD1 (ENTH Domain Containing 1 (ENTHD1))

Reaktivität

Human, Maus, Ratte

Wirt

  • 26
Kaninchen

Klonalität

  • 26
Polyklonal

Konjugat

  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ENTHD1 Antikörper ist konjugiert mit Biotin

Applikation

  • 26
  • 13
  • 10
  • 8
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Kreuzreaktivität

    Human, Maus, Ratte

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human ENTHD1/Epsin2B

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:300-5000
    IHC-P 1:200-400

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Konservierungsmittel

    ProClin

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C for 12 months.

    Haltbarkeit

    12 months
  • Target

    ENTHD1 (ENTH Domain Containing 1 (ENTHD1))

    Andere Bezeichnung

    Epsin2B

    Hintergrund

    Synonyms: CACNA1I, ENTD1_HUMAN, ENTH domain containing 1, ENTH domain-containing protein 1, ENTHD1, Epsin 2B, Epsin-2B, Gm1242, Gm86.

    Background: The ENTHD1 gene is conserved in chimpanzee, dog, cow, mouse and rat, and maps to human chromosome 22q13.1. Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

    Gen-ID

    953
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