Lipoprotein Lipase Antikörper
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- Target Alle Lipoprotein Lipase (LPL) Antikörper anzeigen
- Lipoprotein Lipase (LPL)
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Reaktivität
- Human
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser Lipoprotein Lipase Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA
- Aufreinigung
- purified
- Immunogen
- Purified recombinant fragment of LPL expressed in E. coli.
- Klon
- 2C5
- Isotyp
- IgG1
- Top Product
- Discover our top product LPL Primärantikörper
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- Applikationshinweise
- ELISA: 1:10000, WB: 1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- Ascitic fluid containing 0.03 % sodium azide.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- 4°C, -20°C for long term storage
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Lipoprotein lipase variants associated with an endophenotype of hypertension: hypertension combined with elevated triglycerides." in: Human mutation, Vol. 30, Issue 1, pp. 49-55, (2009) (PubMed).
: "Higher post-absorptive skeletal muscle LPL activity in African American vs. non-Hispanic White pre-menopausal women." in: Obesity (Silver Spring, Md.), Vol. 16, Issue 1, pp. 199-201, (2008) (PubMed).
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Lipoprotein lipase variants associated with an endophenotype of hypertension: hypertension combined with elevated triglycerides." in: Human mutation, Vol. 30, Issue 1, pp. 49-55, (2009) (PubMed).
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- Target
- Lipoprotein Lipase (LPL)
- Andere Bezeichnung
- LPL (LPL Produkte)
- Synonyme
- HDLCQ11 antikoerper, LIPD antikoerper, fb62e04 antikoerper, fc49b03 antikoerper, wu:fb62e04 antikoerper, wu:fc49b03 antikoerper, LPL antikoerper, lipd antikoerper, hdlcq11 antikoerper, lpl antikoerper, LOC100223817 antikoerper, lipoprotein lipase antikoerper, LPL antikoerper, Lpl antikoerper, lpl antikoerper
- Hintergrund
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Description: LPL: lipoprotein lipase, also known as LIPD, HDLCQ11. Entrez Protein: NP_000228. It 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.
Aliases: LIPD, HDLCQ11
- Molekulargewicht
- 53.1 kDa
- Gen-ID
- 4023
- HGNC
- 4023
- Pathways
- Lipid Metabolism
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