sequence mutationとは 意味・読み方・使い方

To provide a probe for detection, detecting a gene of detection target including mutation, even when the sequence of the detection target including the mutation having difference of only one base coexists with the sequence of nondetection target which is free of mutation.例文帳に追加

一塩基のみが異なる、変異を含む検出対象配列と変異を含まない非検出対象配列とが共存する場合でも、前記変異を含む検出対象配列を検出可能な検出用プローブを提供する。 - 特許庁

The mutation of the 619th and/or 898th sites in a base sequence having specific mutation positions is detected.例文帳に追加

変異の位置が特定の塩基配列における６１９位および／または８９８位の位置の変異を検出することによる。 - 特許庁

To detect the mutation in the base sequence of the nucleic acid in high throughput in no need of an expensive apparatus.例文帳に追加

高価な装置を用いることなく、かつハイスループットで核酸の塩基配列の変異を検出する。 - 特許庁

A method of detecting Lafora's disease includes a step of detecting a mutation in the nucleic acid sequence.例文帳に追加

当該核酸配列における突然変異を検出する段階を含む、ラフォラ病を検出する方法。 - 特許庁

PERFECT LENGTH SEQUENCE OF HUMAN LAFORA TYPE EPILEPSY- CAUSING GENE AND USE OF MUTATION THEREOF例文帳に追加

ヒト・ラフォーラ型てんかん原因遺伝子完全長配列及びその突然変異の使用 - 特許庁

To provide a method for analyzing the mutation of a double strand nucleic acid fragment, by which a base sequence difference such as gene mutation, gene insertion or gene deletion can be found out at a nucleic acid level to detect a mutation not only for a single strand nucleic acid but also for a double strand nucleic acid.例文帳に追加

遺伝子変異、遺伝子挿入および遺伝子欠失等の塩基配列の違いを核酸レベルで捉え、一本鎖核酸のみならず、二本鎖核酸についても、変異の検出の可能な方法を提供する。 - 特許庁

Consequently mutation polymorphism in a base sequence in each mutation is readily analyzed according to the method of the invention by comparing and measuring degree of expression of a mRNA from other samples.例文帳に追加

従って、ほかの試料から発現されるmRNAの程度を比べて測定できて各々の変異の塩基配列での突然変異多形性(mutation polymorphism)を本発明の方法によって容易に分析できる。 - 特許庁

To provide a method for detecting mutation by which the mutation is more universally and accurately detected in good sensitivity while precisely preventing the synthesis of a complemental strand on an untargeted base sequence even in any nucleic acid sequence in the method for detecting the mutation of a gene by using a LAMP method.例文帳に追加

LAMP法を用いた遺伝子の変異検出方法において、非標的塩基配列上からの相補鎖合成をどのような核酸配列においても確実に防止して、より普遍的に、正確かつ感度の良い変異検出方法を提供すること。 - 特許庁