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Invitrogen™ LPL Polyclonal Antibody

Goat Polyclonal Antibody

Supplier:  Invitrogen™ PA547033

Catalog No. PIPA547033


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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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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