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Invitrogen™ LPL Polyclonal Antibody
Goat Polyclonal Antibody
Supplier: Invitrogen™ PA547033
Description
This antibody detects human Lipoprotein Lipase/LPL in direct ELISAs and less than 1% cross-reactivity with recombinant human (rh) LIPG, rhLIPI, and rhPNLIPRP1 is observed. Reconstitute in sterile PBS to a final concentration of 0.2 mg/mL.
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.
Specifications
LPL | |
Polyclonal | |
Unconjugated | |
LPL | |
adipose lipoprotein lipase; alpha lipase; HDLCQ11; I79_006077; LIPD; lipoprotein lipase; lipoprotein lipase (EC 3.1.1.34); lipoprotein lipase precursor; lipoprotein lipase preprotein; Lipoprotein lipase-like protein; LPL; O 1-4-5; phospholipase A1; triacylglycerol lipase | |
Goat | |
Antigen affinity chromatography | |
RUO | |
16956, 4023 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Lyophilized |
Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
0.2 mg/mL | |
PBS with 5% trehalose and No Preservative | |
P06858, P11152 | |
LPL | |
E. coli-derived recombinant human Lipoprotein Lipase/LPL. | |
100 μg | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
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