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C16orf57 anticorps (AA 1-265)

L’anticorps Lapin Polyclonal anti-C16orf57 a été validé pour WB. Il convient pour détecter C16orf57 dans des échantillons de Humain.
N° du produit ABIN6149979

Aperçu rapide pour C16orf57 anticorps (AA 1-265) (ABIN6149979)

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
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-265

    Séquence

    MSAAPLVGYS SSGSEDESED GMRTRPGDGS HRRGQSPLPR QRFPVPDSVL NMFPGTEEGP EDDSTKHGGR VRTFPHERGN WATHVYVPYE AKEEFLDLLD VLLPHAQTYV PRLVRMKVFH LSLSQSVVLR HHWILPFVQA LKARMTSFHR FFFTANQVKI YTNQEKTRTF IGLEVTSGHA QFLDLVSEVD RVMEEFNLTT FYQDPSFHLS LAWCVGDARL QLEGQCLQEL QAIVDGFEDA EVLLRVHTEQ VRCKSGNKFF SMPLK

     Réactivité croisée

    Humain, Souris

    Attributs du produit

    Polyclonal Antibodies

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-265 of human USB1 (NP_078874.2).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

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

    Autre désignation

    USB1

    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.,USB1,C16orf57,HVSL1,Mpn1,PN,hUsb1,Cell Biology & Developmental Biology,USB1

    Poids moléculaire

    20 kDa/28 kDa/30 kDa

    ID gène

    79650

    UniProt

    Q9BQ65
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