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C14orf2 antibody

C14orf2 Reactivity: Human, Mouse ELISA, IHC, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7248335
  • Target See all C14orf2 products
    C14orf2 (Chromosome 14 Open Reading Frame 2 (C14orf2))
    Reactivity
    • 28
    • 10
    • 1
    Human, Mouse
    Host
    • 28
    Rabbit
    Clonality
    • 28
    Polyclonal
    Conjugate
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This C14orf2 antibody is un-conjugated
    Application
    • 13
    • 10
    • 9
    • 5
    • 1
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human C14orf2
    Isotype
    IgG
  • Application Notes
    WB 1:500-1:2000, IHC 1:40-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.1 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    C14orf2 (Chromosome 14 Open Reading Frame 2 (C14orf2))
    Alternative Name
    C14orf2 (C14orf2 Products)
    Synonyms
    MP68 antibody, PLPM antibody, MLQ antibody, 9430003J03Rik antibody, AU043134 antibody, AV124504 antibody, Mp68 antibody, chromosome 14 open reading frame 2 antibody, chromosome 21 open reading frame, human C14orf2 antibody, RIKEN cDNA 2010107E04 gene antibody, C14orf2 antibody, C21H14orf2 antibody, 2010107E04Rik antibody
    Background
    C14orf2, also known as MP68, MP68 is a 58 amino acid mitochondrial protein that belongs to the small mitochondrial proteolipid family. The gene encoding MP68 maps to human chromosome 14, which houses over 700 genes and comprises nearly 3.5 % of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 7 kDa

    UniProt
    P56378
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