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C16orf57 anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement C16orf57 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN5517969

Aperçu rapide pour C16orf57 anticorps (N-Term) (ABIN5517969)

Antigène

Voir toutes C16orf57 (USB1) Anticorps
C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Reactivité

  • 25
  • 18
  • 18
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 22
  • 2
  • 1
Lapin

Clonalité

  • 25
Polyclonal

Conjugué

  • 8
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp C16orf57 est non-conjugé

Application

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

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

    Séquence

    LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG

    Purification

    Affinity purified

    Immunogène

    The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    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.
  • Antigène

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

    Autre désignation

    C16ORF57

    Sujet

    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

    ID gène

    79650

    NCBI Accession

    NM_001195302, NP_001182231
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