|Purification||>95% pure (SDS-PAGE). Protein G Chromatography|
|Target/Specificity||Recognizes LPS of virulent and vaccine strains of Fr. tularensis. In immunofluorescence studies clone FB11 does not display any cross-reactivity with Fr. novicida, Br. abortus, Br. suis, Br. melitensis, Br. ovis, Y. pestis, Y. entercolitica, Y. pseudotuberculosis, E. coli, V. cholerae. The binding site for clone FB11 is located on the O-antigen polysaccharide chain which consists of tetrasaccharide fragments and has the following structure: -4) alpha-D-GalpNAcAN- (1-4)-alpha-D-GalpNAcAN- (1-3)-beta-D- QuipNAc- (1-2)-beta-Quip4NF m- (1). Tetrasaccharide D-GalpNAcAN-(1-4)-alpha-D- GalpNAcAN- (1-3)-beta-D-QuipNAc-(1-2)-beta-D-Quip4NFm and trisaccharide D-GalpNAcAN-(1-3)-beta-D-QuipNAc-(1-2)-beta-D-Quip4NFm compete in ELISA for binding clone FB11 with LPS of Fr. tularensis.|
|Preservative||0.1% Sodium Azide|
|Storage||Store at 2-8°C.|
|Precautions||Monoclonal Antibody to LPS Francisella tularensis [FB11] is for research use only and not for use in diagnostic or therapeutic procedures.|
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The reference listed below is for research purposes only:Hotta, Akitoyo, et al., (2007), “Preparation of Monoclonal Antibodies for Detection and Identification of Francisella tularensis”, Clinical and Vaccine Immunology, 14(1), 81-84.
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