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All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.

LAMP-2 Antibody

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CAT. NO.: AMA-0216

Product Details
Size	100 µg
Reactivity	Human, Mouse
Host	Rabbit
Source/Isotype	Rabbit IgG1
Storage	Store at -20°C.
Purification	Affinity chromatography purified via peptide column.

Usage
Application	WB, IHC, ELISA
Product Usage Information Dilution	Western Blotting (1-2 μg/mL); Immunofluorescence (10 μg/mL)

Background
Autophagy, the process of bulk degradation of cellular proteins throμgh an autophagosomic-lysosomal pathway is important for normal growth control and may be defective in tumor cells. It is involved in the preservation of cellular nutrients under starvation conditions as well as the normal turnover of cytosolic components and is negatively regulated by TOR (Target of rapamycin). LAMP-2, a highly glycosylated protein associated with the lysosome, has recently been shown to be important in autophagy as mice deficient in this protein failed to convert autophagic vacuoles into vacuoles leading to impaired degradation of long-lived proteins. This correlates with the finding that human LAMP-2 deficiency causing Danon's disease is associated with the accumulation of autophagic material in striated myocytes. LAMP-2 exists in multiple isoforms.

Background

Autophagy, the process of bulk degradation of cellular proteins throμgh an autophagosomic-lysosomal pathway is important for normal growth control and may be defective in tumor cells. It is involved in the preservation of cellular nutrients under starvation conditions as well as the normal turnover of cytosolic components and is negatively regulated by TOR (Target of rapamycin). LAMP-2, a highly glycosylated protein associated with the lysosome, has recently been shown to be important in autophagy as mice deficient in this protein failed to convert autophagic vacuoles into vacuoles leading to impaired degradation of long-lived proteins. This correlates with the finding that human LAMP-2 deficiency causing Danon's disease is associated with the accumulation of autophagic material in striated myocytes. LAMP-2 exists in multiple isoforms.

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All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.