Abstract:
본 발명은 국화황화모틀바이로이드(Chrysanthemum chlorotic mottle viroids, CChMVd)의 변이주(Strain)를 중합효소연쇄반응 및 제한효소 절편길이 다형성(Polymerase chain reaction-Restriction fragment length polymorphism, PCR-RFLP)법을 이용하여 구별하는 방법에 관한 것이다. 본 발명에 따른 방법을 이용하면 효과적으로 국화황화모틀바이로이드의 5개 변이주인 msim34, SSHA6, Beijing, India 669541, India 646404를 구별할 수 있다. 따라서 국화재배농가에 막대한 피해를 주고 있는 국화 감염성 바이로이드를 조기에 신속하고 정확하게 검출 가능하게 하여, 막대한 경제 손실을 현저히 감소시킬 수 있을 것으로 기대된다.
Abstract:
The present invention relates to a primer set for an isothermal amplification reaction to detect Chrysanthemum stunt viroid (CSVd), a composition comprising the primer set, and a method for detecting CSVd using the composition. When the primer set for an isothermal amplification reaction to detect CSVd according to the present invention is used, the CSVd can be effectively detected without technical equipment on the spot for a short period of time. In addition, viroids can be detected even with a small amount of sample, and the diagnostic results can be promptly verified by the naked eye under the natural light by using a high-concentration of SYBR Green I. Therefore, Chrysanthemum infectious viroids that seriously damage Chrysanthemum farmhouses can be detected early, promptly, and accurately, thereby significantly reducing a huge economic loss due to the Chrysanthemum infectious viroids.
Abstract translation:本发明涉及用于检测菊花特发性类病毒(CSVd)的等温扩增反应的引物组,包含引物组的组合物,以及使用该组合物检测CSVd的方法。 当使用根据本发明的用于检测CSVd的等温扩增反应的引物时,可以在没有技术设备的情况下,在现场短时间内有效地检测CSVd。 此外,即使使用少量的样品也能够检测到病毒,并且通过使用高浓度的SYBR Green I,可以在自然光下通过肉眼迅速验证诊断结果。因此,严重损害菊花感染性病毒 可以及早,准确地检测到菊花农舍,从而大大减少了菊花感染性病毒的巨大经济损失。
Abstract:
The present invention relates to viral genome sequences of tomato yellow leaf curl virus Korea isolate DNA-A inducing leaf curling, honeysuckle yellow vein mosaic virus Korea isolate beta-satellite DNA, and a recombinant plasmid including the same. The present invention can induce virus infection in various plant bodies and can be applied to various studies including the prevention of virus by using the various plant bodies.
Abstract:
PURPOSE: An acquired lymphedema animal model and a method for producing the same are provided to form bigger edema than the lymphedema animal and look like a real model. CONSTITUTION: An acquired lymphedema animal model uses an animal without subcutaneous and lymphatic vessel by an iron and lymphatic vessel in the right leg and the right inguinal region. The animal is mammal and especially a mouth. A manufacturing method of the same comprises the following steps. The superficial inguinal node, deep inguinal node and popliteal node are cut. The right leg lymphatic vessel is blocked. To use the iron subcutaneous and lymphatic vessel are removed.
Abstract:
PURPOSE: A primer composition for loop-mediated isothermal amplification for detecting Chrysanthemum chlorotic mottle viroid, and a use thereof are provided to quickly diagnose using high concentration SYBR Green I with naked eye under natural light. CONSTITUTION: A primer set for loop-mediated isothermal amplification for detecting Chrysanthemum chlorotic mottle viroid contains sequence in sequence numbers 1-4. The Chrysanthemum chlorotic mottle viroid is SSHA6 strains or msim34 strains. A primer composition for loop-mediated isothermal amplification for detecting Chrysanthemum chlorotic mottle viroid contains the primer set. The composition further contains DNA polymerase, dNTPs, and a reaction buffer.
Abstract translation:目的:用于环路介导的等温扩增用于检测菊花褪绿斑马疹的底漆组合物,并提供其用途,在自然光下用肉眼快速诊断高浓度SYBR Green I。 构成:用于检测菊花褪绿斑马疹的环介导等温扩增的引物组包含序列号1-4中的序列。 菊花褪绿斑马疹是SSHA6菌株或msim34菌株。 用于检测菊花褪绿斑驳病毒的环介导等温扩增的底漆组合物含有引物组。 该组合物还含有DNA聚合酶,dNTP和反应缓冲液。
Abstract:
PURPOSE: A primer set for detecting begomovirus is provided to accurately and quickly diagnose begomovirus infection from plant samples. CONSTITUTION: A primer set for detecting begomovirus comprises one or more kinds of primer sets selected among a primer set of: sequence numbers 1 and 2; sequence numbers 3 and 4; sequence numbers 5 and 6; sequence number 7 and 8; sequence numbers 9 and 10; sequence number 11 and 12; sequence numbers 13 and 14; sequence number 15 and 16; sequence numbers 17 and 18; and sequence numbers 19 and 20. The begomovirus includes tomato leaf curl virus, tomato yellow leaf curl virus, tobacco leaf curl virus, honeysuckle yellow vein virus, or sweet potato leaf curl virus.
Abstract:
PURPOSE: A gene which is derived from sweet potato leaf curl infection DNA virus with an activity of suppressing gene silence after transcription is provided to obtain AC2 gene with sequence of the sequence number 16. CONSTITUTION: A gene derived from a sweet potato leaf curl infection DNA virus with an activity of suppressing gene silence after transcription is AC2 gene having sequence of the sequence number 16. An AC2 protein derived from a sweet potato leaf curl infection DNA virus is denoted by the sequence of the sequence number 17.
Abstract:
본발명은토마토잎말림뉴델리바이러스 DNA-A 및 DNA-B를접종할수 있는감염성클론및 이의용도에관한것이다. 본발명의토마토잎말림뉴델리바이러스 DNA-A 및 DNA-B(ToLCNDV DNA-A 및 DNA-B)의염기서열을포함하는재조합플라스미드및 이를포함하는대장균및 아그로박테리움튜머페이션스를이용시, 매개충(insect vector) 없이도효과적으로작물에토마토잎말림뉴델리바이러스 DNA-A 및 DNA-B의감염을유발시킬수 있다. 따라서, 본발명을이용하여토마토잎말림뉴델리바이러스 DNA-A 및 DNA-B의기주범위및 기주와의상관관계등 다양한연구에응용할수 있으며, 이를통해바이러스감염으로인한경제적손실을사전에방지할수 있어, 관련분야에유용하게이용할수 있다.