2005
DOI: 10.1016/j.peptides.2004.10.028
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Identification of immunodominant regions of Brassica juncea glyoxalase I as potential antitumor immunomodulation targets

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Cited by 5 publications
(3 citation statements)
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“…The most common types of filter or chromatography paper used for SPOT synthesis are Whatman 50, Whatman 540 and *Address correspondence to this author at the Kinexus Bioinformatics Corporation, 8755 Ash Street, Suite 1, Vancouver, BC V6P 6T3, Canada; Tel: +604-323-2547 ext.17; Fax: +604-323-2548; E-mail: peptides@kinexus.ca CHR1 [23][24][25][26]. N-methyl-imidazole (NMI) [27,28]. These functional groups are the only groups accessible for the build-up of peptide chains on cellulose.…”
Section: Modification Of the Cellulose Membranementioning
confidence: 99%
See 1 more Smart Citation
“…The most common types of filter or chromatography paper used for SPOT synthesis are Whatman 50, Whatman 540 and *Address correspondence to this author at the Kinexus Bioinformatics Corporation, 8755 Ash Street, Suite 1, Vancouver, BC V6P 6T3, Canada; Tel: +604-323-2547 ext.17; Fax: +604-323-2548; E-mail: peptides@kinexus.ca CHR1 [23][24][25][26]. N-methyl-imidazole (NMI) [27,28]. These functional groups are the only groups accessible for the build-up of peptide chains on cellulose.…”
Section: Modification Of the Cellulose Membranementioning
confidence: 99%
“…N-terminal acetylation is carried out like capping by treatment of the protected peptide with acetic anhydride at various concentrations [27,54] and often with DIPEA as a basic additive [69] after final Fmoc deprotection. N-terminal acetylation is carried out like capping by treatment of the protected peptide with acetic anhydride at various concentrations [27,54] and often with DIPEA as a basic additive [69] after final Fmoc deprotection.…”
Section: Selected Peptide Modificationsmentioning
confidence: 99%
“…Hence, in many cases synthetic peptides or peptidomimetics, which mimic the sequence of the binding site of any given protein, demonstrate the same biological activity as the protein itself, although sometimes with partial loss of activity. Therefore, arrays of synthetic peptides offer a fast and easy possibility to screen for protein interactions [129], binding regions (epitopes) [130,131] and enzyme activities [132,133]. Moreover, they allow the screening for inhibitors [134] and the engineering of antibodies, enzymes or inhibitors [135] with regard to modified binding sites.…”
Section: Peptide Microarraysmentioning
confidence: 99%