Lipoprotein Lipase (LPL) Peptide
LPL
Reactivity: Mammalian
Host: Synthetic
BP, WB, IHC
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- Target See all Lipoprotein Lipase (LPL) products
- Lipoprotein Lipase (LPL)
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- LGYEINKVRA KRSSKMYLKT RSQMPYKVFH YQVKIHFSGT ESETHTNQAF
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of LPL antibody,
Alternative Names: LPL control peptide, LPL antibody Blocking Peptide, Anti-LPL Blocking Peptide, lipoprotein lipase Blocking Peptide, HDLCQ11 Blocking Peptide, LIPD Blocking Peptide
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- Application Notes
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20 °C long term.
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- Target
- Lipoprotein Lipase (LPL)
- Synonyms
- HDLCQ11 Peptide, LIPD Peptide, fb62e04 Peptide, fc49b03 Peptide, wu:fb62e04 Peptide, wu:fc49b03 Peptide, LPL Peptide, lipd Peptide, hdlcq11 Peptide, lpl Peptide, LOC100223817 Peptide, lipoprotein lipase Peptide, LPL Peptide, Lpl Peptide, lpl Peptide
- 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.
- Molecular Weight
- 50 kDa
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