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NBPF6 anticorps (N-Term)

NBPF6 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2791691
  • Antigène Voir toutes NBPF6 Anticorps
    NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))
    Épitope
    • 2
    • 1
    • 1
    • 1
    N-Term
    Reactivité
    • 12
    • 1
    Humain
    Hôte
    • 12
    Lapin
    Clonalité
    • 12
    Polyclonal
    Conjugué
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp NBPF6 est non-conjugé
    Application
    • 5
    • 2
    Western Blotting (WB)
    Séquence
    EKVQESPAPR EVQKTEEKEV PQDSLEECAV TCSNSHNPSN SNQPHRSTKI
    Homologie
    Human: 100%
    Attributs du produit
    This is a rabbit polyclonal antibody against NBPF6. It was validated on Western Blot.
    Purification
    Affinity Purified
    Immunogène
    The immunogen is a synthetic peptide directed towards the N-terminal region of Human NBPF6
    Top Product
    Discover our top product NBPF6 Anticorps primaire
  • Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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.
    Conseil sur la manipulation
    Avoid repeat freeze-thaw cycles.
    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
    NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))
    Autre désignation
    NBPF6 (NBPF6 Produits)
    Synonymes
    anticorps NBPF member 6, anticorps NBPF6
    Sujet
    This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, mental retardation, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies.
    Alias Symbols: -
    Protein Size: 638
    Poids moléculaire
    70 kDa
    ID gène
    653149
    NCBI Accession
    NM_001143988, NP_001137460
    UniProt
    Q5VWK0
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