Figure 3
Figure 3. Alignment of nucleotide sequences and translation of IG heavy chain CDR3. DNA extracted from lung explant specimens was amplified using the FR1/JH BIOMED-2 PCR protocol. After purification, PCR fragments were directly sequenced. (A) Sequences were aligned to immunoglobulin sequences using IMGT/V-QUEST18 and IMGT/JunctionAnalysis,19 from IMGT, the international ImMunoGeneTics information system (http://imgt.cines.fr). Somatic mutations were defined as nucleotide substitutions after elimination of the known polymorphisms described in the IMGT database.20 (B) The same database determines the ability of sequences to code for functional heavy chains. First line includes amino acid positions according to the IMGT unique numbering for V-DOMAIN.21

Alignment of nucleotide sequences and translation of IG heavy chain CDR3. DNA extracted from lung explant specimens was amplified using the FR1/JH BIOMED-2 PCR protocol. After purification, PCR fragments were directly sequenced. (A) Sequences were aligned to immunoglobulin sequences using IMGT/V-QUEST18  and IMGT/JunctionAnalysis,19  from IMGT, the international ImMunoGeneTics information system (http://imgt.cines.fr). Somatic mutations were defined as nucleotide substitutions after elimination of the known polymorphisms described in the IMGT database.20  (B) The same database determines the ability of sequences to code for functional heavy chains. First line includes amino acid positions according to the IMGT unique numbering for V-DOMAIN.21 

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