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C16orf57 Antikörper (N-Term)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch C16orf57 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN5517969

Kurzübersicht für C16orf57 Antikörper (N-Term) (ABIN5517969)

Target

Alle C16orf57 (USB1) Antikörper anzeigen
C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Reaktivität

  • 25
  • 18
  • 18
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 22
  • 2
  • 1
Kaninchen

Klonalität

  • 25
Polyklonal

Konjugat

  • 8
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser C16orf57 Antikörper ist unkonjugiert

Applikation

  • 21
  • 13
  • 4
  • 3
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    N-Term

    Sequenz

    LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG

    Aufreinigung

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

    Andere Bezeichnung

    C16ORF57

    Hintergrund

    This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

    Alias Symbols: PN, Mpn1, HVSL1, hUsb1, C16orf57

    Protein Size: 186

    Gen-ID

    79650

    NCBI Accession

    NM_001195302, NP_001182231
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