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CPT2 antibody

CPT2 Reactivity: Human, Mouse, Rat WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2425697
  • Target See all CPT2 Antibodies
    CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))
    Reactivity
    • 66
    • 34
    • 21
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 61
    • 5
    • 2
    Rabbit
    Clonality
    • 55
    • 13
    Polyclonal
    Conjugate
    • 35
    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This CPT2 antibody is un-conjugated
    Application
    • 47
    • 36
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human CPT2
    Isotype
    IgG
    Top Product
    Discover our top product CPT2 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.7 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))
    Alternative Name
    CPT2 (CPT2 Products)
    Synonyms
    CPT1 antibody, CPTASE antibody, IIAE4 antibody, AI323697 antibody, CPTII antibody, cg2107 antibody, wu:fa03e08 antibody, wu:fb54a02 antibody, zgc:101627 antibody, carnitine palmitoyltransferase 2 antibody, carnitine O-palmitoyltransferase 2, mitochondrial antibody, carnitine palmitoyltransferase 2 S homeolog antibody, CPT2 antibody, LOC100214547 antibody, Cpt2 antibody, cpt2.S antibody, cpt2 antibody
    Background
    The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders.
    Molecular Weight
    Calculated MW: 74 kDa
    NCBI Accession
    NP_000089
    Pathways
    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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