Lipoprotein Lipase Antikörper (AA 300-327)
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- Target Alle Lipoprotein Lipase (LPL) Antikörper anzeigen
- Lipoprotein Lipase (LPL)
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Bindungsspezifität
- AA 300-327
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Lipoprotein Lipase Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
- Kreuzreaktivität (Details)
- Expected species reactivity: Mouse, Rat, Bovine, Pig
- Aufreinigung
- Antigen affinity purified
- Immunogen
- A portion of amino acids 300-327 from the human protein was used as the immunogen for this LPL antibody.
- Isotyp
- Ig Fraction
- Top Product
- Discover our top product LPL Primärantikörper
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- Applikationshinweise
- Titration of the LPL antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:10-1:50,Flow Cytometry: 1:10-1:50
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- In 1X PBS, pH 7.4, with 0.09 % 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
- -20 °C
- Informationen zur Lagerung
- Aliquot the LPL antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
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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
- 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].
- UniProt
- P06858
- Pathways
- Lipid Metabolism
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