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Lipoprotein Lipase antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects Lipoprotein Lipase in WB. It exhibits reactivity toward Human.
Catalog No. ABIN926449

Quick Overview for Lipoprotein Lipase antibody (C-Term) (ABIN926449)

Target

See all Lipoprotein Lipase (LPL) Antibodies
Lipoprotein Lipase (LPL)

Reactivity

  • 88
  • 32
  • 25
  • 19
  • 6
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 71
  • 27
  • 2
Rabbit

Clonality

  • 65
  • 35
  • 1
Polyclonal

Conjugate

  • 52
  • 8
  • 7
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Lipoprotein Lipase antibody is un-conjugated

Application

  • 78
  • 37
  • 34
  • 31
  • 27
  • 18
  • 14
  • 14
  • 10
  • 8
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 16
    • 9
    • 6
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
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    C-Term

    Purification

    Purified

    Immunogen

    LPL antibody was raised in rabbit using the C terminal of LPL as the immunogen
  • Application Notes

    Optimal conditions should be determined by the investigator.

    Comment

    LPL Blocking Peptide, catalog no. 33R-5003, is also available for use as a blocking control in assays to test for specificity of this LPL antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Concentration

    Lot specific

    Buffer

    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.

    Handling Advice

    Avoid repeated freeze/thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target

    Lipoprotein Lipase (LPL)

    Alternative Name

    LPL

    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. Synonyms: Polyclonal LPL antibody, Anti-LPL antibody, lipoprotein lipase antibody, HDLCQ11 antibody, LIPD antibody.

    Pathways

    Lipid Metabolism
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