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DYNAP Antikörper (N-Term)

Der Kaninchen Polyklonal Anti-DYNAP-Antikörper wurde für WB validiert. Er ist geeignet, DYNAP in Proben von Human zu detektieren.
Produktnummer ABIN1539422

Kurzübersicht für DYNAP Antikörper (N-Term) (ABIN1539422)

Target

DYNAP (Dynactin Associated Protein (DYNAP))

Reaktivität

Human

Wirt

  • 17
Kaninchen

Klonalität

  • 17
Polyklonal

Konjugat

  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DYNAP Antikörper ist unkonjugiert

Applikation

  • 9
  • 8
  • 1
  • 1
Western Blotting (WB)

Klon

RB35932
  • Bindungsspezifität

    • 7
    • 2
    • 2
    AA 6-34, N-Term

    Aufreinigung

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This C18orf26 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 6-34 amino acids from the N-terminal region of human C18orf26.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    C18orf26 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Haltbarkeit

    6 months
  • Target

    DYNAP (Dynactin Associated Protein (DYNAP))

    Andere Bezeichnung

    C18orf26

    Hintergrund

    C18orf26 (chromosome 18 open reading frame 26) is a 210 amino acid single pass membrane protein that is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

    Gen-ID

    284254

    NCBI Accession

    NP_775900

    UniProt

    Q8N1N2
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