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Invitrogen™ LPL Polyclonal Antibody
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Catalog No. PIPA547033
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100 μg
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PIPA547033 100 μg
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Catalog No. PIPA547033 Supplier Invitrogen™ Supplier No. PA547033
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Goat Polyclonal Antibody

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

Antigen LPL
Applications Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry
Classification Polyclonal
Concentration 0.2 mg/mL
Conjugate Unconjugated
Formulation PBS with 5% trehalose and No Preservative
Gene LPL
Gene Accession No. P06858, P11152
Gene Alias 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
Gene Symbols LPL
Host Species Goat
Immunogen E. coli-derived recombinant human Lipoprotein Lipase/LPL.
Purification Method Antigen affinity chromatography
Quantity 100 μg
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 16956, 4023
Target Species Human, Mouse
Content And Storage -20°C, Avoid Freeze/Thaw Cycles
Product Type Antibody
Form Lyophilized
Isotype IgG
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