ANPEP Mouse Monoclonal Antibody

ANPEP Mouse Monoclonal Antibody

Cat: AMM81419
Size:50μL Price:$168
Size:100μL Price:$300
Application:ELISA,FC

Reactivity:Human
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:ANPEP
Category: Mouse Monoclonal Antibody Tags:

Summary

Production Name

ANPEP Mouse Monoclonal Antibody

Description

Mouse monoclonal Antibody

Host

Mouse

Application

ELISA,FC

Reactivity

Human

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Mouse IgG1

Clonality

Monoclonal

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Purified antibody in PBS with 0.05% sodium azide.

Purification

Affinity Purification

 

Immunogen

Gene Name

ANPEP

Alternative Names

APN; CD13; LAP1; P150; PEPN; GP150

Gene ID

290

SwissProt ID

P15144

 

Application

Dilution Ratio

ELISA 1:5000-1:20000,FC 1:200-1:400

Molecular Weight

110kDa

 

Background

Aminopeptidase N is located in the small-intestinal and renal microvillar membrane, and also in other plasma membranes. In the small intestine aminopeptidase N plays a role in the final digestion of peptides generated from hydrolysis of proteins by gastric and pancreatic proteases. Its function in proximal tubular epithelial cells and other cell types is less clear. The large extracellular carboxyterminal domain contains a pentapeptide consensus sequence characteristic of members of the zinc-binding metalloproteinase superfamily. Sequence comparisons with known enzymes of this class showed that CD13 and aminopeptidase N are identical. The latter enzyme was thought to be involved in the metabolism of regulatory peptides by diverse cell types, including small intestinal and renal tubular epithelial cells, macrophages, granulocytes, and synaptic membranes from the CNS. Human aminopeptidase N is a receptor for one strain of human coronavirus that is an important cause of upper respiratory tract infections. Defects in this gene appear to be a cause of various types of leukemia or lymphoma.

 

Research Area

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