Lipoprotein Lipase (LPL) Peptide
LPL
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
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- Antigène Tous les produits Lipoprotein Lipase (LPL)
- Lipoprotein Lipase (LPL)
- Type de proteíne
- Synthetic
- Origine
- Mammifères
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Séquence
- LGYEINKVRA KRSSKMYLKT RSQMPYKVFH YQVKIHFSGT ESETHTNQAF
- Attributs du produit
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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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- Indications d'application
- 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
- Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20 °C long term.
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- Antigène
- Lipoprotein Lipase (LPL)
- Synonymes
- 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
- Sujet
- 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.
- Poids moléculaire
- 50 kDa
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