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Human tissue extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with LPL antibody (GTX101125) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
Human tissue extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with LPL antibody (GTX101125) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
Human tissue extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with LPL antibody (GTX101125) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

LPL antibody

GTX101125
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityChicken, Human, Mouse, Sheep
TargetLPL
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Overview

  • Supplier
    GeneTex
  • Product Name
    LPL antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.11 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4023
  • Target name
    LPL
  • Target description
    lipoprotein lipase
  • Target synonyms
    HDLCQ11, LIPD, lipoprotein lipase, phospholipase A1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP06858
  • Protein Name
    Lipoprotein lipase
  • Scientific Description
    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]
  • Reactivity
    Chicken, Human, Mouse, Sheep
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    41116161

Datasheet

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