Polymorphism of human C2 detected by immunoblotting

[1]  D. Paty,et al.  Study of alleles of the second complement component (C2) on Canadian HLA haplotypes. , 2008, Tissue antigens.

[2]  G. O'Neill.  C4 Polymorphism: Use of a Monoclonal Antibody to Distinguish C4A and C4B Locus Products , 1984, Vox sanguinis.

[3]  H. Towbin,et al.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[4]  C. Rittner,et al.  Polymorphism of the Second Component of Human Complement (C2) , 1979, Vox sanguinis.

[5]  P. Schur,et al.  Mapping of the structural gene for the second component of complement with respect to the human major histocompatibility complex. , 1979, American journal of human genetics.

[6]  C. Alper,et al.  Evidence for a silent or null gene in hereditary C2 deficiency. , 1978, Journal of immunology.

[7]  J. Dausset,et al.  A haplotype study of HLA complex with special reference to the HLA-DR series and to Bf. C2 and glyoxalase I polymorphisms. , 1978, Tissue antigens.

[8]  Hobart Mj,et al.  Complement genetics in relation to HLA. , 1978 .

[9]  J. Atkinson,et al.  Structural heterogeneity of C2 Complement protein and its genetic variants in man: a new polymorphism of the HLA region. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J. Atkinson,et al.  Mapping of the HLA locus controlling C2 structural variants and linkage disequilibrium between alleles C22 and Bw15 , 1976 .

[11]  C. Alper.  Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf , 1976, The Journal of experimental medicine.