Lipoprotein lipase (LPL) Mouse Monoclonal Antibody (HRP conjugated) [Clone ID: OTI3A10]
CAT#: TA503793BM
LPL (Lipoprotein lipase) mouse monoclonal antibody, clone OTI3A10 (formerly 3A10), HRP conjugated
Frequently bought together (3)
Transient overexpression lysate of lipoprotein lipase (LPL)
USD 396.00
Other products for "Lipoprotein lipase"
Specifications
| Product Data | |
| Clone Name | OTI3A10 |
| Applications | FC, IHC, WB |
| Recommended Dilution | WB 1:500, IHC 1:150, FLOW 1:100 |
| 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 HEK293T. |
| Formulation | PBS (pH 7.3) containing 1% BSA, 50% glycerol. |
| Concentration | 0.5 mg/ml |
| Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| Conjugation | HRP |
| 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 |
Documents
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| FAQs |
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