CloneID: MN12H2
Antigen Long Description: The original antibody was generated immunizing mice with outer membrane protein preparations from meningococcal serogroup B, serosubtype P1.7,16 reference strain H44/76.
Buffer Composition: PBS with 0.02% Proclin 300.
Available Custom Conjugation Options: AP, HRP, Fluorescein, APC, PE, Biotin Type A, Biotin Type B, Streptavidin, FluoroProbes 647H, Atto488, APC/Cy7, PE/Cy7
Uniprot Accession No.: E6MXW0
Specificity Statement: This antibody is specific for the amino acid sequence 'TKDTNNNL' derived from the VR2 sequence of sero-subtype P1.16 (residues 180-187) from meningococcal strain H44/76. This antibody binds epitope P1.16 located on PorA surface loop 4 from the serogroup B meningococci of the type Neisseria meningitidis.
Application Notes (Clone): This antibody shows high bactericidal activity. This antibody binds the bacterial membrane surface protein resulting in activation of the classical complement pathway and subsequent lysis of the cell (PMID: 9880525). A study on antibacterial activity of human chimeric IgG1 (chIgG1) and chimeric IgG3 (chIgG3) version of this antibody showed that the serum bactericidal activity of chIgG1 was greater than that of chIgG3, and chIgG3 was better than chIgG1 in terms of opsonophagocytic (PMID: 11342648). This antibody provided protection in vivo against the prototype P1.7,16a, variably against the P1.7,16b and P1.7,16c, but not against the P1.7,16d variants in an infant rat infection model (PMID: 11273739). This antibody and the chimeric hIgG1 and hIgG3 derivatives all induced efficient bactericidal activity in vitro in the presence of human or infant rat complement and augmented bacterial clearance in complement-sufficient HsdBrlHan:WIST rats, while the hIgG4 was unable to do so. In C6-deficient PVG/c− rats, lacking complement-mediated bacterial lysis, the augmentation of bacterial clearance this antibody and chimeric hIgG1 version was impaired compared to that in the syngeneic complement-sufficient PVG/c+ rat strain (PMID: 16622217).
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