![]() ![]() rhizogenes silvestre, 15 no con el T-DNA de pCAMBIA que lleva el gen l1 clonado. ![]() Este resultado sugiere que estos tejidos habían sido transformado solo con el T-DNA de A. El ensayo de β-glucuronidasa, como se esperaba, resultó negativo en comparación con raíces transformadas con el vector pCAMBIA 1105.1 vacío (Figura 6 A). rhizogenes transformadas con la construcción pCAMHPV16L1 murieron cuando se pusieron en contacto con higromicina, que es el marcador de selección para raíces transformadas con el vector pCAMBIA 1105.1. La mayoría de las raíces que se indujeron por punción de hipocotilos de plántulas con la cepa de A. B, Ensayo de β –glucuronidasa y morfología microscópica de raíces de brócoli transformadas positivamente (b, c) con el gen de la proteína l1 observadas al microscopio óptico a 100X. 238000003786 synthesis reaction Methods 0.A, Microfotografías 25X y 100X después del ensayo de β–glucuronidasa de raíces no transformadas (a) y transformadas negativamente con gen l1 del HPV (b), en comparación con raíces transformadas con el vector pCAMBIA (c).229920002106 messenger RNA Polymers 0.000 claims abstract description 13.108020004999 Messenger RNA Proteins 0.000 claims abstract description 13.125000003275 alpha amino acid group Chemical group 0.000 claims abstract description 15.125000000266 alpha-aminoacyl group Chemical group 0.000 claims abstract description 24.238000010348 incorporation Methods 0.000 claims abstract description 60.229920001184 polypeptide Polymers 0.000 claims abstract description 99.229920002892 amber Polymers 0.000 claims abstract description 109.108020004705 Codon Proteins 0.000 claims abstract description 150.241000203407 Methanocaldococcus jannaschii Species 0.000 claims abstract description 197.150000001413 amino acids Chemical class 0.000 claims abstract description 431.238000004519 manufacturing process Methods 0.000 title description 13.102000003960 Ligases Human genes 0.000 title claims description 279.229920001949 Transfer RNA Polymers 0.000 title claims abstract description 392.Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.) Filing date Publication date Priority to US28503001P priority Critical Priority to US285030P priority Priority to US35551402P priority Priority to US355514P priority Application filed by University of California, Scripps Research Institute filed Critical University of California Application granted granted Critical Publication of ES2464532T3 publication Critical patent/ES2464532T3/en Anticipated expiration legal-status Critical Status Expired - Lifetime legal-status Critical Current Links Original Assignee University of California Scripps Research Institute Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.) Meggers Ryan Aaron Mehl Miro Pastrnak Stephen William Santoro Zhiwen Zhang Current Assignee (The listed assignees may be inaccurate. Inventor Peter Schultz Lei Wang John Christopher Anderson Jason W. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.) Expired - Lifetime Application number ES09006800.8T Other languages Spanish ( es) #Ensayo de comparacion y contraste pdf#Methods and compositions for the production of orthogonal pairs of tRNA-aminoacyl-tRNA synthetaseĭownload PDF Info Publication number ES2464532T3 ES2464532T3 ES09006800.8T ES09006800T ES2464532T3 ES 2464532 T3 ES2464532 T3 ES 2464532T3 ES 09006800 T ES09006800 T ES 09006800T ES 2464532 T3 ES2464532 T3 ES 2464532T3 Authority ES Spain Prior art keywords trna amino acid synthetase unnatural amino amino acids Prior art date Legal status (The legal status is an assumption and is not a legal conclusion. ![]()
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |