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NBPF15 antibody (N-Term)

NBPF15 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2791696
  • Target See all NBPF15 products
    NBPF15 (Neuroblastoma Breakpoint Family, Member 15 (NBPF15))
    Binding Specificity
    N-Term
    Reactivity
    Human
    Host
    • 1
    Rabbit
    Clonality
    • 1
    Polyclonal
    Conjugate
    • 1
    This NBPF15 antibody is un-conjugated
    Application
    Western Blotting (WB)
    Sequence
    VQKLSPENDN DDDEDVQVEV AEKVQKSSAP REMQKAEEKE VPEDSLEECA
    Predicted Reactivity
    Human: 100%
    Characteristics
    This is a rabbit polyclonal antibody against NBPF16. It was validated on Western Blot.
    Purification
    Affinity Purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the N-terminal region of human NBPF15
  • 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
    NBPF15 (Neuroblastoma Breakpoint Family, Member 15 (NBPF15))
    Alternative Name
    NBPF16 (NBPF15 Products)
    Synonyms
    AB14 antibody, NBPF member 15 antibody, NBPF15 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. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes.
    Alias Symbols: AG3, AB14, NBPF16
    Protein Size: 670
    Molecular Weight
    73 kDa
    Gene ID
    284565
    NCBI Accession
    NM_001170755, NP_001164226
    UniProt
    Q5SXJ2
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