Hi Li, I'd recommend another T-cell marker (say some CD3 component, or CD4/CD8 if you want to differentiate subtypes). Back in the day I worked in a lab which did a lot of CDR lenght spectratyping ("immunoscope") within various V region subgroups of the same clinical sample cDNA (looking for clonal expansion). I recall suggesting they use the non-variable part of the TCR to quantitate the distribution of the various V gene subgroups versus the total T-cell group (as the spectra show clonal expansion within V gene groups, but the technique cannot compare abundance across several V gene groups), but I cannot remember if there was a technical problem (such as degree of conservation, conserved region lenght etc) or if they just decided to stick with something that worked well enough for them. Guy ------------------------------------ Ablynx NV Guy Hermans, PhD Senior Scientist guy.hermans@ablynx.com Technologiepark 4 B-9052 Zwijnaarde Belgium tel: +32 (0)9 262 00 00 fax: +32 (0)9 262 00 01 mobile: +32 (0)486 788 551 ------------------------------------ -----Original Message----- From: chen li [mailto:chen_li3@yahoo.com] Sent: Tuesday, January 29, 2008 00:03 To: cyto-inbox Subject: a gene conserved and unique to T cells Hi all, Sorry this is a Flow question. I want to quantify the T cell number within PBMCs background based on genomic DNA. Is it possible to find a gene/fragment which is conserved in all the naive/mature T cells and also unique to T cells, but not in other cells based on TCR rearrangement( or other theory) ? Thank you in advance, Li ________________________________________________________________________ ____________ Looking for last minute shopping deals? Find them fast with Yahoo! Search. http://tools.search.yahoo.com/newsearch/category.php?category=shoppingReceived on Wed Jan 30 12:38:00 2008
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