Mouse Monoclonal LPL antibody [2C5] (STJ98222)

$379.00

Reactivity: Human
Applications: WB, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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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

Image descriptions:

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Alternative names:

Check alternative names for the antibody

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LPL antibody, LIPD antibody,|EC 3.1.1 antibody|EC 3.1.1.34 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|

 

Name

LPL Monoclonal Antibody

Catalogue No.

STJ98222

Reactivity

Human

Specificity

LPL Monoclonal Antibody detects endogenous levels of LPL protein.

Immunogen

Purified recombinant fragment of LPL expressed in E Coli

Host

Mouse

Applications

WB, ELISA

Recommended dilution

WB 1:500-1:2000; ELISA 1:10000

Clonality

Monoclonal

Conjugation

Unconjugated

Isotype

IgG1

Formulation

LPL Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.

Concentration

1 mg/ml

Purification

LPL Antibody was purified using affinity purification.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Lipoprotein lipase antibody, LPL antibody,

Database links

Human UniProt/Swiss-Prot:P06858;Mouse UniPort/Swiss-Prot: P11152;Rat UniProt/Swiss-Port: Q06000;Human Entrez Gene: 4023;Mouse Entrez Gene: 16956;Rat Entrez Gene: Rn.3834

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

Research area

All research areas>Synthesis and Degradation>LPL
(View all antibody categories related to Synthesis and Degradation)

Note

AntibodyPlus can customize LPL Antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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