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DPY19L1 Antikörper (AA 354-657)

Dieser Kaninchen Polyklonal Antikörper erkennt spezifisch DPY19L1 in WB, ELISA, IHC und FACS. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7601445
500,50 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 8 bis 11 Werktagen

Kurzübersicht für DPY19L1 Antikörper (AA 354-657) (ABIN7601445)

Target

Alle DPY19L1 Antikörper anzeigen
DPY19L1 (Dpy-19-Like 1 (C. Elegans) (DPY19L1))

Reaktivität

  • 34
  • 6
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 34
Kaninchen

Klonalität

  • 34
Polyklonal

Konjugat

  • 11
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DPY19L1 Antikörper ist unkonjugiert

Applikation

  • 29
  • 15
  • 13
  • 13
  • 9
  • 8
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)
  • Bindungsspezifität

    • 15
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 354-657

    Verwendungszweck

    Anti-DPY19L1 Antibody

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-DPY19L1 Antibody (ABIN7601445). Tested in ELISA, Flow Cytometry, IHC, WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human DPY19L1 recombinant protein (Position: L354-H657).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human
    Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Konzentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    DPY19L1 (Dpy-19-Like 1 (C. Elegans) (DPY19L1))

    Andere Bezeichnung

    DPY19L1

    Hintergrund

    Synonyms: Kelch repeat and BTB domain-containing protein 2, BTB and kelch domain-containing protein 1, KBTBD2, BKLHD1, KIAA1489

    Tissue Specificity: Detected in liver, skeletal muscle, kidney, pancreas, spleen, thyroid, testis, ovary, small intestine and colon.

    Background: Dpy-19 (dumpy-19), is a 683 amino acid C. elegans protein that is required to orient the neuroblasts QL and QR correctly on the anterior/posterior axis. Dpy-19 is expressed highly in dorsal hyp7 cells, ventral P cells and lateral V cells, and dorsal and ventral body muscle cells. DPY19L1 (Dpy-19-like protein 1), also known as KIAA0877, is a 675 amino acid multi-pass membrane protein that belongs to the Dpy-19 family. DPY19L1 is expressed as two isoforms produced by alternative splicing and is encoded by a gene mapping to human chromosome 7, which encodes over 1,000 genes and makes up about 5 % of the human genome. Diseases associated with chromosome 7 include Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

    Molekulargewicht

    77 kDa

    Gen-ID

    23333

    Pathways

    SARS-CoV-2 Protein Interaktom
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