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1. (WO2019032054) METHOD FOR SCREENING SPLICING VARIANTS OR EVENTS
국제사무국에 기록된 최신 서지정보    정보 제출

공개번호: WO/2019/032054 국제출원번호: PCT/SG2018/050408
공개일: 14.02.2019 국제출원일: 13.08.2018
IPC:
C12Q 1/6813 (2018.01) ,C12N 15/113 (2010.01)
[IPC code unknown for C12Q 1/6813]
C SECTION C — 화학; 야금
12
생화학; 맥주; 주정; 포도주; 식초; 미생물학; 효소학; 돌연변이 또는 유전자공학
N
미생물 또는 효소; 그 조성물; 미생물의 보존, 유지, 증식; 돌연변이 또는 유전자공학; 배지
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돌연변이 또는 유전공학; 유전자 공학과 관련된 DNA 또는 RNA, 벡터, 예. 플라스미드 또는 그것의 분리, 조제, 정제; 그것을 위한 숙주의 이용
09
.재조합 DNA 기술
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유전자 조작된 형태의 DNA 혹은 RNA 단편
113
유전자의 발현을 조절하는 넌-코딩 핵산, 예. 안티센스 올리고뉴클레오티드
출원인:
AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH [SG/SG]; 1 Fusionopolis Way, #20-10 Connexis North Tower Singapore 138632, SG
발명자:
WEE, Keng Boon; SG
대리인:
AMICA LAW LLC; 77 Robinson Road #22-01 Robinson 77 Singapore 068896, SG
우선권 정보:
10201706585X11.08.2017SG
발명의 명칭: (EN) METHOD FOR SCREENING SPLICING VARIANTS OR EVENTS
(FR) PROCÉDÉ DE CRIBLAGE DE VARIANTS OU D'ÉVÉNEMENTS D'ÉPISSAGE
요약서:
(EN) The present invention relates to a high-throughput method of screening splicing variants of target genes as drug targets or for characterisation of their biological functions. The disclosure provides a method for the screening of splicing variants, comprising: (a) providing a first antisense oligonucleotide capable of inducing a first splice event on the target gene to express a first splicing variant, and a second antisense oligonucleotide capable of inducing a second splice event on the target gene to express a second splicing variant; (b) hybridising the first and second antisense oligonucleotides to a pre-mRNA of the target gene; and (c) characterising the effect of the splice event. In one embodiment, the first antisense oligonucleotide switches the splice event that expresses the second splicing variant towards one that expresses the first splicing variant, while the second antisense oligonucleotide switches the splice event that expresses the first splicing variant towards one that expresses the second splicing variant.
(FR) La présente invention concerne un procédé à haut rendement de criblage de variants d'épissage de gènes cibles en tant que cibles de médicament ou pour caractériser leurs fonctions biologiques. L'invention concerne un procédé de criblage de variants d'épissage consistant (a) à fournir un premier oligonucléotide antisens capable d'induire un premier événement d'épissage sur le gène cible pour exprimer un premier variant d'épissage, et un second oligonucléotide antisens capable d'induire un second événement d'épissage sur le gène cible pour exprimer un second variant d'épissage; (b) à hybrider les premier et second oligonucléotides antisens à un pré-ARNm du gène cible; et (c) à caractériser l'effet de l'événement d'épissage. Dans un mode de réalisation, le premier oligonucléotide antisens fait passer l'événement d'épissage qui exprime le second variant d'épissage vers un qui exprime le premier variant d'épissage, tandis que le second oligonucléotide antisens fait passer l'événement d'épissage qui exprime le premier variant d'épissage vers un qui exprime le second variant d'épissage.
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지정국: AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW
아프리카지역 지식재산권기구(ARIPO) (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW)
유라시아 특허청 (AM, AZ, BY, KG, KZ, RU, TJ, TM)
유럽 특허청(EPO) (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR)
African Intellectual Property Organization (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG)
공개언어: 영어 (EN)
출원언어: 영어 (EN)