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OriGene Antibodies in recent publications
A common polymorphism in the LDL receptor gene has multiple effects on LDL receptor function Hum. Mol. Genet., Apr 2013; 22: 1424 - 1431. [anti-DDK]

Excitotoxicity Upregulates SARM1 Protein Expression and Promotes Wallerian-Like Degeneration of Retinal Ganglion Cells and Their Axons Invest. Ophthalmol. Vis. Sci., Apr 2013; 54: 2771 - 2780. [SARM1]

Modulation of TET2 expression and 5-methylcytosine oxidation by the CXXC domain protein IDAX Nature 497, 122-126 doi:10.1038/nature12052 [anti-DDK]

Natriuretic Peptide Receptor-3 Gene (NPR3): Nonsynonymous Polymorphism Results in Significant Reduction in Protein Expression Because of Accelerated Degradation Circ Cardiovasc Genet, Apr 2013; 6: 201 - 210. [NPR3]

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Home All anti-LAMP2 antibodies

Anti-LAMP2 Antibody

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA306261
  • Rabbit Polyclonal LAMP-2 Antibody
100ug $325 3-7 Days Add to Shopping Cart
WB(1)
IHC(1)
Gene NameHomo sapiens lysosomal-associated membrane protein 2 (LAMP2), transcript variant C
Synonyms:CD107b; LAMP-2; LAMPB; LGP110
ImmunogenLAMP-2 antibody was raised against a 17 amino acid peptide from near the carboxy of human LAMP-2.
BufferPBS containing 0.02% sodium azide.
Clone Name IsotypeIgG
Species ReactivityHuman, Mouse Concentration1ug/ul
Purification Affinity chromatography purified via peptide column (Protein A or G Sepharose)
Guaranteed Application *WB, IHC Suggested DilutionsWB: 1-2 ug/ml; ICC: 10ug/ml
BackgroundAutophagy, the process of bulk degradation of cellular proteins through 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 (1,2) and is negatively regulated by TOR (Target of rapamycin) (3). LAMP-2, a highly glycosylated protein associated with the lysosome (4), has recently been shown to be important in autophagy as mice deficient in this protein failed to convert autophagic vacuoles into vacuoles (5) 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 (6). LAMP-2 exists in multiple isoforms (7).
Related Pathway
Hemostasis
Senescence and Autophagy

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WB Image
Western blot analysis of LAMP-2 in HepG2 cell lysate with LAMP-2 antibody at (A) 1 and (B) 2 ug/ml.
IHC Image
Immunocytochemistry of LAMP-2 in HepG2 cells with LAMP-2 antibody at 10 ug/ml.

 

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