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NBPF6 antibody (C-Term)

NBPF6 Reactivity: Human, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2791688
  • Target See all NBPF6 Antibodies
    NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))
    Binding Specificity
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reactivity
    Human, Rat
    Host
    • 12
    Rabbit
    Clonality
    • 12
    Polyclonal
    Conjugate
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NBPF6 antibody is un-conjugated
    Application
    • 5
    • 2
    Western Blotting (WB)
    Sequence
    STLYSFEDKQ VSLALVDKIK KDQEEIEDQS PPCPRLSQEL PEVKEQEVPE
    Predicted Reactivity
    Human: 100%, Rat: 75%
    Characteristics
    This is a rabbit polyclonal antibody against NBPF6. It was validated on Western Blot.
    Purification
    Affinity Purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the C-terminal region of Human NBPF6
    Top Product
    Discover our top product NBPF6 Primary Antibody
  • 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.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeat freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    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.
  • Target
    NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))
    Alternative Name
    NBPF6 (NBPF6 Products)
    Synonyms
    NBPF member 6 antibody, NBPF6 antibody
    Background
    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: 667
    Molecular Weight
    75 kDa
    Gene ID
    653149
    NCBI Accession
    NM_001143987, NP_001137459
    UniProt
    E9PDL3
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