Genomic DNA extraction from Mycobacterium avium v1 (protocols.io.bupvnvn6)

protocols.io ◽  
2021 ◽  
Author(s):  
Tetsuya Komatsu ◽  
Kenji not provided ◽  
Justice not provided ◽  
Shota not provided ◽  
Kotaro not provided ◽  
...  
2021 ◽  
Author(s):  
Tetsuya Komatsu ◽  
Kenji Ohya ◽  
Justice Opare Odoi ◽  
Shota Suganuma ◽  
Kotaro Sawai ◽  
...  

Mycobacterium avium subsp. hominissuis (MAH) is one of the most important agents causing non-tuberculosis mycobacterial infection in human and pigs. Genome analysis on MAH of human isolates has been proceeding, however, those of pigs are limited despite its potential source of infection to human. Here, we isolated MAH from pig lymph nodes or livers and obtained their genomes.


2013 ◽  
Vol 19 (6) ◽  
pp. 1068-1073
Author(s):  
Xiaolan KONG ◽  
Zuozhi CHEN ◽  
Lin LIN ◽  
Chunhou LI ◽  
Peiwen LIANG

2012 ◽  
Vol 29 ◽  
pp. S220
Author(s):  
Karlygash Aubakirova ◽  
Madina Omasheva ◽  
Natalya Ryabushkina ◽  
Laura Yerbolova ◽  
Tolepbergen Tazhibaev ◽  
...  

2014 ◽  
Vol 42 (2) ◽  
pp. 472-477 ◽  
Author(s):  
Zhou SHUMIN ◽  
Chu YANXIA ◽  
Zheng BANG ◽  
Zhang WEI

Tobacco (Nicotiana tabacum) cv. ‘Bright Yellow 2’ (BY2) cell suspension is a useful system to study the structure and function of plant cell. However, low efficiency of Agrobacterium-mediated transformation, and transgene silencing during subculture limit its application. Here we present optimization of the traditional protocols of Agrobacterium-mediated transformation and genomic DNA extraction. The transforming efficiency and recovery ratio of genomic DNA extraction were substantially increased by these improvements. Southern assay demonstrated that copy number of transgene could be determined unambiguously. Meanwhile by monitoring the GFP fluorescence we found that the GFP expression can keep stable in suspension culture cells for at least 20 days in liquid medium. Finally, applicability of constitutive promoters of Arabidopsis thaliana UBIQUITIN10 (AtUBQ10) and ARABIDOPSISSKP1 HOMOLOGUE1 (AtASK1) also can drive stable GFP expression in vivo of BY2 cells like CaMV 35S promoter in this plant system./span>


2010 ◽  
Vol 3 (1) ◽  
pp. 37-39 ◽  
Author(s):  
Gustavo Agostini ◽  
Raquel Lüdtke ◽  
Sergio Echeverrigaray ◽  
Tatiana Teixeira de Souz-Chies

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