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DYNAP Antikörper (N-Term)

DYNAP Reaktivität: Human WB, EIA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN950798
  • Target Alle DYNAP Produkte
    DYNAP (Dynactin Associated Protein (DYNAP))
    Bindungsspezifität
    • 8
    • 7
    • 6
    AA 5-34, N-Term
    Reaktivität
    Human
    Wirt
    • 22
    Kaninchen
    Klonalität
    • 22
    Polyklonal
    Konjugat
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser DYNAP Antikörper ist unkonjugiert
    Applikation
    • 14
    • 13
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    Spezifität
    This antibody reacts to C18orf26.
    Kreuzreaktivität (Details)
    Species reactivity (tested):Human.
    Aufreinigung
    Affinity chromatography on Protein A
    Immunogen
    KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human C18orf26
    Isotyp
    Ig Fraction
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.25 mg/mL
    Buffer
    PBS containing 0.09 % (W/V) sodium azide as preservative
    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 the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target
    DYNAP (Dynactin Associated Protein (DYNAP))
    Andere Bezeichnung
    C18orf26 (DYNAP Produkte)
    Synonyme
    C18orf26 antikoerper, dynactin associated protein antikoerper, DYNAP antikoerper
    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.Synonyms: Uncharacterized protein
    Gen-ID
    284254
    NCBI Accession
    NP_775900
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