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DGCR14 anticorps (AA 217-244)

DGCR14 Reactivité: Humain WB Hôte: Lapin Polyclonal RB21365 unconjugated
N° du produit ABIN657859
  • Antigène Voir toutes DGCR14 Anticorps
    DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))
    Épitope
    • 6
    • 6
    • 6
    • 6
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 217-244
    Reactivité
    • 20
    • 3
    • 2
    Humain
    Hôte
    • 19
    • 1
    Lapin
    Clonalité
    • 20
    Polyclonal
    Conjugué
    • 10
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp DGCR14 est non-conjugé
    Application
    • 20
    • 15
    • 1
    • 1
    Western Blotting (WB)
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogène
    This DGCR14 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 217-244 amino acids from the Central region of human DGCR14.
    Clone
    RB21365
    Isotype
    Ig Fraction
    Top Product
    Discover our top product DGCR14 Anticorps primaire
  • Indications d'application
    WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Stockage commentaire
    DGCR14 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
    Date de péremption
    6 months
  • Antigène
    DGCR14 (DiGeorge Syndrome Critical Region Gene 14 (DGCR14))
    Autre désignation
    DGCR14 (DGCR14 Produits)
    Sujet
    This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus.
    Poids moléculaire
    52568
    ID gène
    8220
    NCBI Accession
    NP_073210
    UniProt
    Q96DF8
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