Lipoprotein lipase (LPL) Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI4H3]
CAT#: TA503787AM
LPL (Lipoprotein lipase) mouse monoclonal antibody, clone OTI4H3 (formerly 4H3), Biotinylated
Other products for "LPL"
Specifications
Product Data | |
Clone Name | OTI4H3 |
Applications | IHC, WB |
Recommended Dilution | WB 1:2000, IHC 1:150 |
Reactivities | Human, Mouse, Rat |
Host | Mouse |
Isotype | IgG1 |
Clonality | Monoclonal |
Immunogen | Human recombinant protein fragment corresponding to amino acids 28-475 of human LPL(NP_000228) produced in E.coli. |
Formulation | PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide. |
Concentration | 0.5 mg/ml |
Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
Conjugation | Biotin |
Storage | Store at -20°C as received. |
Stability | Stable for 12 months from date of receipt. |
Predicted Protein Size | 50.3 kDa |
Gene Name | lipoprotein lipase |
Database Link | |
Background | 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] |
Synonyms | HDLCQ11; LIPD |
Reference Data | |
Protein Families | Druggable Genome |
Protein Pathways | Alzheimer's disease, Glycerolipid metabolism, PPAR signaling pathway |
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