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CPT2 antibody (AA 212-241)

CPT2 Reactivity: Human WB Host: Rabbit Polyclonal RB41839 unconjugated
Catalog No. ABIN1881226
  • Target See all CPT2 Antibodies
    CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))
    Binding Specificity
    • 10
    • 10
    • 8
    • 8
    • 6
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 212-241
    Reactivity
    • 74
    • 34
    • 21
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 69
    • 5
    • 2
    Rabbit
    Clonality
    • 64
    • 12
    Polyclonal
    Conjugate
    • 33
    • 8
    • 7
    • 6
    • 5
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This CPT2 antibody is un-conjugated
    Application
    • 55
    • 46
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Predicted Reactivity
    Pr
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This CPT2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 212-241 amino acids from the Central region of human CPT2.
    Clone
    RB41839
    Isotype
    Ig Fraction
    Top Product
    Discover our top product CPT2 Primary Antibody
  • Application Notes
    WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Expiry Date
    6 months
  • Lan, Fu, Liu, Huang, Chang, Liu, Peng, Chen: "High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy." in: Clinical genetics, Vol. 78, Issue 6, pp. 565-9, (2010) (PubMed).

    Bailey, Xie, Do, Montpetit, Diaz, Mohan, Keavney, Yusuf, Gerstein, Engert, Anand: "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study." in: Diabetes Care, Vol. 33, Issue 10, pp. 2250-3, (2010) (PubMed).

    Ruaño, Thompson, Kane, Pullinger, Windemuth, Seip, Kocherla, Holford, Wu: "Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the ACACB gene on low-density lipoprotein cholesterol?" in: Pharmacogenomics, Vol. 11, Issue 7, pp. 959-71, (2010) (PubMed).

    Hogan, Vladutiu: "Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutation." in: Anesthesia and analgesia, Vol. 109, Issue 4, pp. 1070-2, (2009) (PubMed).

    Talmud, Drenos, Shah, Shah, Palmen, Verzilli, Gaunt, Pallas, Lovering, Li, Casas, Sofat, Kumari, Rodriguez, Johnson, Newhouse, Dominiczak, Samani, Caulfield, Sever, Stanton, Shields, Padmanabhan et al.: "Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. ..." in: American journal of human genetics, Vol. 85, Issue 5, pp. 628-42, (2009) (PubMed).

  • Target
    CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))
    Alternative Name
    CPT2 (CPT2 Products)
    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
    73777
    NCBI Accession
    NP_000089
    UniProt
    P23786
    Pathways
    Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
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