Author: Funaro, Ada; Gribaudo, Giorgio; Luganini, Anna; Ortolan, Erika; Lo Buono, Nicola; Vicenzi, Elisa; Cassetta, Luca; Landolfo, Santo; Buick, Richard; Falciola, Luca; Murphy, Marianne; Garotta, Gianni; Malavasi, Fabio
Title: Generation of potent neutralizing human monoclonal antibodies against cytomegalovirus infection from immune B cells Document date: 2008_11_12
ID: 1u2fkwx3_39
Snippet: The variable regions of heavy chain (VH) and light chain (VL) of mAb 26A1 were sequenced according the technology established by Fusion Antibodies Ltd. Briefly, frozen cells pellets (~5 × 10 4 cells) were used for extracting total RNA with STAT-60 RNA extraction reagent. cDNA was produced by reverse transcription with an oligo(d)T primer. PCR reactions were set up to amplify VH and VL regions with a mix of IgG-and Igk/λ specific primers, respec.....
Document: The variable regions of heavy chain (VH) and light chain (VL) of mAb 26A1 were sequenced according the technology established by Fusion Antibodies Ltd. Briefly, frozen cells pellets (~5 × 10 4 cells) were used for extracting total RNA with STAT-60 RNA extraction reagent. cDNA was produced by reverse transcription with an oligo(d)T primer. PCR reactions were set up to amplify VH and VL regions with a mix of IgG-and Igk/λ specific primers, respectively. The PCR products of two amplification reactions were cloned using a Eco RI restriction site in a sequencing vector (pCR2.1; Invitrogen) and used for transforming TOP10 E. coli cells, following the manufacturer's instructions. A consensus sequence was determined from at least ten clones. The resulting DNA sequences were aligned and translated into protein sequences enabling the generation of consensus DNA and protein sequence for VH 26A1 and VL 26A1. The VH 26A1 and VL 26A1 protein sequences were compared and aligned with sequences present in the GenomeQuest, GeneSeq, and EBI databases. The CDRs characterizing VH 26A1 and VL 26A1 protein sequences were predicted by the IMGT database [54] .
Search related documents:
Co phrase search for related documents- restriction site and reverse transcription: 1, 2
- restriction site and sequence vector: 1, 2, 3
- reverse transcription and RNA extraction reagent: 1, 2
- reverse transcription and sequence vector: 1
- reverse transcription and specific primer: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43
- reverse transcription and total RNA extract: 1, 2, 3, 4
- reverse transcription and variable region: 1, 2, 3, 4, 5
- reverse transcription and VH heavy chain: 1
- reverse transcription and VL light chain: 1
- sequence vector and specific primer: 1
- variable region and VH heavy chain: 1, 2
- variable region and VH heavy chain variable region: 1, 2
- variable region and VL light chain: 1
- variable region and VL region: 1, 2
- VH heavy chain and VL light chain: 1, 2, 3, 4, 5, 6, 7, 8
- VH heavy chain and VL region: 1
- VH heavy chain variable region and VL light chain: 1
- VH heavy chain variable region and VL region: 1
- VL light chain and VL region: 1
Co phrase search for related documents, hyperlinks ordered by date