No products in the cart.
Mouse Monoclonal LPL antibody [2C5] (STJ98222)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-1:2000; ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for LPL Monoclonal Antibody.
Check alternative names for the antibodyExpand
LPL antibody, LIPD antibody,|EC 3.1.1 antibody|EC 184.108.40.206 antibody|HDLCQ11 antibody|LIPD antibody|LIPL_HUMAN antibody|Lipoprotein lipase antibody|LPL antibody|LPL protein antibody|MGC137861 antibody|Anti-Lipoprotein lipase antibody [LPL.A4] (ab21356)
SCBT cat No: sc-73646|sc-81780|sc-373759|sc-32885|sc-58780|sc-32382|
LPL Monoclonal Antibody
|Catalogue No.|| |
LPL Monoclonal Antibody detects endogenous levels of LPL protein.
Purified recombinant fragment of LPL expressed in E Coli
|Recommended dilution|| |
WB 1:500-1:2000; ELISA 1:10000
LPL Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
LPL Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Lipoprotein lipase antibody, LPL antibody,
|Protein names|| |
Lipoprotein lipase , LPL ,
|Protein function|| |
The primary function of this lipase is the hydrolysis of triglycerides of circulating chylomicrons and very low density lipoproteins (VLDL). Binding to heparin sulfate proteogylcans at the cell surface is vital to the function. The apolipoprotein, APOC2, acts as a coactivator of LPL activity in the presence of lipids on the luminal surface of vascular endothelium (By similarity). / Triacylglycerol + H2O = diacylglycerol + a carboxylate.
|Involvement in disease|| |
Lipoprotein lipase deficiency (LPL deficiency) [MIM:238600]: Recessive disorder usually manifesting in childhood. On a normal diet, patients often present with abdominal pain, hepatosplenomegaly, lipemia retinalis, eruptive xanthomata, and massive hypertriglyceridemia, sometimes complicated with acute pancreatitis. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the AB hydrolase superfamily. Lipase family. / Contains 1 PLAT domain.
|Protein post-translational modifications|| |
Tyrosine nitration after lipopolysaccharide (LPS) challenge down-regulates the lipase activity.
|Protein cellular localization|| |
Cell membrane / Secreted
AntibodyPlus can customize LPL Antibody according to your requirement, including bulk product size,etc. Please contact email@example.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.
St John’s Laboratory Ltd.
|Product type|| |
There are no reviews for this product yet.
By submitting a review, get following benefits:
1. Receive $50 ABcoins as credit for each review.
2. First trial sample order will be fully refunded as credit.
3. Have a chance to win a $50 amazon gift card!
There is no extra validation for this product yet.
Check other extra validated antibodies below: