Lipoprotein lipase Recombinant Protein (H00004023-P01)
Lipoprotein lipase Recombinant Protein
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Lipoprotein lipase Recombinant Protein Summary: | | | Specificity: | LPL (NP_000228.1, 1 a.a. - 475 a.a.) recombinant protein with a ~26kD N-terminal GST tag. |
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| | Note: Not all species have been tested for usefulness with this product. Only those species listed have been tested. We cannot make any guarantees about additional reactivities which may or may not occur. |
View Additional Lipoprotein lipase Products Lipoprotein lipase Recombinant Protein Details: | Immunogen: | This protein is not active and should not be used for experiments requiring activity. |
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| Uses: | Useful in Western Blot and ELISA. This protein has not been tested for any functionality. This product may contain endotoxins and is not suitable for use with live cells. |
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| Dilutions: | ELISA,
Western Blot |
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| Unit Size: | 2 ug |
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| Concentration: | Please see the vial label for concentration. |
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Notes: This product is produced by and distributed for Abnova, a company based in Taiwan. Packaging: | Storage: | Store at -80 °C. Avoid freeze-thaw cycles. |
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| Buffer: | 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. |
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| Limitations: | This product is for research use only and is not approved for use in humans or in clinical diagnosis. Products are guaranteed for 6 months from date of receipt, except for peptides and proteins which are guaranteed for 3 months. |
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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]
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