Title of article :
Immunochemical analysis of CD107a (LAMP-1)
Author/Authors :
Parkinson-Lawrence، نويسنده , , Emma J. and Dean، نويسنده , , Caroline J. and Chang، نويسنده , , Melissa and Hopwood، نويسنده , , John J. and Meikle، نويسنده , , Peter J. and Brooks، نويسنده , , Doug A.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
6
From page :
161
To page :
166
Abstract :
CD107a, also known as the lysosome associated membrane protein-1 (LAMP-1), is expressed largely in the endosome–lysosome membranes of cells, but is also found on the plasma membrane (1–2% of total LAMP-1). LAMP-1 has been implicated in a variety of cellular functions, including cancer metastasis. It has been proposed as a therapeutic agent for some cancers, and is a marker for lysosomal storage disorders and different cell types such as cytotoxic T cells. In light of this diversity of applications, it is important to have well characterized immune-reagents for the detection and quantification of LAMP-1. We have compared a new monoclonal antibody 80280 against LAMP-1 to an existing monoclonal antibody BB6 and a rabbit polyclonal antibody. While all antibodies gave similar results by immunofluorescence, the monoclonal antibody 80280 showed no epitope reactivity to LAMP-1 peptides, suggesting the possibility of a carbohydrate epitope. Western blotting revealed a weaker activity of the monoclonal antibody 80280 relative to either the BB6 monoclonal or the polyclonal antibodies. The monoclonal antibody 80280 is distinct from BB6, providing an additional reagent for CD107a analysis.
Keywords :
Western blotting , immunofluorescence , Lysosomal membrane associated protein , CD107a , Epitope map
Journal title :
Cellular Immunology
Serial Year :
2005
Journal title :
Cellular Immunology
Record number :
1848220
Link To Document :
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