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1.
Artículo en Inglés | MEDLINE | ID: mdl-24438282

RESUMEN

Korean native cattle is one of the famous native breeds in Korean. In the present work, we report the complete mitochondrial genome sequence of Korean native cattle for the first time. The total length of the mitogenome was 16,339 bp with the base composition of 33.4% for A, 27.2% for T, 26.0% for C, and 13.4% for G, and an A-T (60.6%)-rich feature was detected. It harbored 13 protein-coding genes, 2 ribosomal RNA genes, 22 transfer RNA genes and 1 non-coding control region (D-loop region). The arrangement of all genes was identical to the typical mitochondrial genomes of cattle. The complete mitochondrial genome sequence of Korean native cattle would serve as an important data set of the germplasm resources for further study.


Asunto(s)
Bovinos/genética , Genoma Mitocondrial/genética , Análisis de Secuencia de ADN , Animales , Genes de ARNr , Corea (Geográfico) , Anotación de Secuencia Molecular , Datos de Secuencia Molecular , Sistemas de Lectura Abierta/genética , ARN de Transferencia/genética , Banco de Semillas
2.
Sheng Wu Gong Cheng Xue Bao ; 22(4): 598-603, 2006 Jul.
Artículo en Chino | MEDLINE | ID: mdl-16894894

RESUMEN

HIV-TAT protein transduction domain (PTD) is a new kind of peptide that is responsible for transduction of proteins through the plasma membrane with high efficiency. Linked covalently to proteins, peptides, nucleic acid, it could transduce into nearly all kinds of cells and tissues with high efficiency and without any damages. In this study, we constructed the TAT-EDAG and TAT-GFP prokaryotic expression vectors and expressed soluble TAT-EDAG and TAT-GFP fusions in E. coli BL21 (DE3) successfully. By using the Ni-NTA-agrose purification system under the native condition we got the purified fusion proteins whose purification were higher than 90%. After desalting we found the TAT-GFP could transduced successfully into the mouse fibroblast cells and the TAT-EDAG could transduced into HL-60 cells in vitro. It will be useful to amplify the HSCs in vitro in the next step.


Asunto(s)
Proteínas Nucleares/genética , Proteínas Recombinantes de Fusión/biosíntesis , Transducción Genética , Productos del Gen tat del Virus de la Inmunodeficiencia Humana/genética , Animales , Escherichia coli/genética , Fibroblastos/metabolismo , Células HL-60 , Humanos , Ratones , Proteínas Recombinantes de Fusión/aislamiento & purificación
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