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Lipoprotein Lipase antibody

LPL Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7101626
  • Target See all Lipoprotein Lipase (LPL) Antibodies
    Lipoprotein Lipase (LPL)
    Reactivity
    • 72
    • 28
    • 22
    • 16
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 59
    • 17
    • 2
    Rabbit
    Clonality
    • 55
    • 24
    Monoclonal
    Conjugate
    • 35
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Lipoprotein Lipase antibody is un-conjugated
    Application
    • 62
    • 33
    • 32
    • 23
    • 15
    • 14
    • 14
    • 8
    • 7
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Cross-Reactivity
    Human, Mouse
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human Lipoprotein lipase (LPL) (LPL)
    Isotype
    IgG
    Top Product
    Discover our top product LPL Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    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
    Lipoprotein Lipase (LPL)
    Alternative Name
    LPL (LPL Products)
    Synonyms
    HDLCQ11 antibody, LIPD antibody, fb62e04 antibody, fc49b03 antibody, wu:fb62e04 antibody, wu:fc49b03 antibody, LPL antibody, lipd antibody, hdlcq11 antibody, lpl antibody, LOC100223817 antibody, lipoprotein lipase antibody, LPL antibody, Lpl antibody, lpl antibody
    Background
    LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq, Jul 2008],HDLCQ11, LIPD,Cancer,Cardiovascular,Endocrine & Metabolism,Endocrine and metabolic diseases,Endocrine and metabolic diseases_Obesity,Lipid Metabolism,Lipid Metabolism_Lipases,Lipids,Mesenchymal Stem Cells,Neurodegenerative Diseases,Neuroscience,Signal Transduction,Stem Cells,LPL
    Molecular Weight
    53 kDa
    Gene ID
    4023
    UniProt
    P06858
    Pathways
    Lipid Metabolism
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