Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

Nhs anticorps

Nhs Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6293547
  • Antigène Voir toutes Nhs Anticorps
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Reactivité
    Humain
    Hôte
    • 1
    • 1
    Lapin
    Clonalité
    • 1
    • 1
    Polyclonal
    Conjugué
    • 2
    Cet anticorp Nhs est non-conjugé
    Application
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human NHS
    Isotype
    IgG
    Top Product
    Discover our top product Nhs Anticorps primaire
  • Indications d'application
    WB 1:200 - 1:2000
    Commentaires

    Detected at low levels in all tissues analyzed, Detected in fetal and adult brain, lens, retina, retinal pigment epithelium, placenta, lymphocytes and fibroblasts, Levels in retinal pigment epithelium, placenta, lymphocytes, and fibroblasts are very low, Expressed also in kidney, lung and thymus

    Restrictions
    For Research Use only
  • 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 -20C. Avoid freeze / thaw cycles.
  • Antigène
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Autre désignation
    NHS (Nhs Produits)
    Synonymes
    anticorps CTRCT40, anticorps CXN, anticorps SCML1, anticorps NHS actin remodeling regulator, anticorps NHS
    Sujet
    This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
    Poids moléculaire
    179.135 kDa
    ID gène
    4810
    UniProt
    Q6T4R5
Vous êtes ici:
Support technique