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Mouse Anti-PNLIP Recombinant Antibody (4I2) (CBMAB-P2253-YC)

Provided herein is a Mouse monoclonal antibody against Human Pancreatic Lipase. The antibody can be used for immunoassay techniques, such as ELISA.
See all PNLIP antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
4I2
Antibody Isotype
IgG1
Application
ELISA

Basic Information

Immunogen
Human pancreatic lipase EC number: 3.1.1.3
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at-20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Pancreatic Lipase
Introduction
PNLIP is a member of the lipase family of proteins. The encoded enzyme is secreted by the pancreas and hydrolyzes triglycerides in the small intestine, and is essential for the efficient digestion of dietary fats. Inhibition of the encoded enzyme may prevent high-fat diet-induced obesity in mice and result in weight loss in human patients with obesity. Mutations in this gene cause congenital pancreatic lipase deficiency, a rare disorder characterized by steatorrhea.
Entrez Gene ID
5406
UniProt ID
P16233
Alternative Names
PTL; Pancreatic Triacylglycerol Lipase; Triacylglycerol Acylhydrolase
Function
Plays an important role in fat metabolism. It preferentially splits the esters of long-chain fatty acids at positions 1 and 3, producing mainly 2-monoacylglycerol and free fatty acids, and shows considerably higher activity against insoluble emulsified substrates than against soluble ones.
Biological Process
Intestinal cholesterol absorptionIEA:Ensembl
Lipid catabolic processManual Assertion Based On ExperimentIBA:GO_Central
Lipid metabolic processManual Assertion Based On ExperimentIMP:UniProtKB
Positive regulation of triglyceride lipase activityManual Assertion Based On ExperimentIDA:CACAO
Cellular Location
Secreted
Involvement in disease
Pancreatic lipase deficiency (PNLIPD):
An autosomal recessive disorder characterized by exocrine pancreatic failure. Clinical findings include oily/greasy stools from infancy or early childhood, absence of discernible pancreatic disease, and significantly decreased pancreatic lipolytic activity.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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