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    • 9. 发明授权
    • Screening for functional antisense agents
    • 筛选功能性反义试剂
    • US06416951B1
    • 2002-07-09
    • US09623385
    • 2001-03-26
    • Gunter SchmidtAndrew Hugin Thompson
    • Gunter SchmidtAndrew Hugin Thompson
    • C12Q168
    • C12Q1/6816C12Q1/6837Y10S977/924C12Q2565/601C12Q2563/173C12Q2525/207C12Q2565/515
    • Provided is a method for identifying a functional antisense agent, which method comprises hybridizing an RNA with an aligonucleotide probe and measuring in real time the kinetics of hybridization, wherein the kinetics are measured by either hybridizing in the presence of an intercalation dye and recording a change in the spectroscopic properties of the dye as hybridizing proceeds, or incorporating a label in either the RNA or the probe, attaching the non-labelled RNA or non-labelled probe to a solid support, generating an evanescent wave in the proximity of the non-labelled RNA or non-labelled probe and recording the increase in a signal generated by interaction of the evanescent wave with the label, as hybridization proceeds.
    • 提供了一种用于鉴定功能性反义剂的方法,该方法包括将RNA与寡核苷酸探针杂交并实时测量杂交的动力学,其中通过在插入染料存在下杂交并记录变化来测量动力学 在作为杂交进行的染料的光谱性质中,或者在RNA或探针中掺入标记,将非标记的RNA或未标记的探针附着到固体支持物上,在非接触的情况下产生ev逝波, 标记的RNA或非标记的探针,并记录随着杂交进行而通过ev逝波的相互作用产生的信号与标记的增加。
    • 10. 发明授权
    • Nucleic acid sequencing
    • 核酸测序
    • US07094531B1
    • 2006-08-22
    • US09341641
    • 1998-01-15
    • Gunter SchmidtAndrew Hugin Thompson
    • Gunter SchmidtAndrew Hugin Thompson
    • C12Q1/68C12N15/00C12N15/63C12N1/20C07H21/04
    • C12Q1/6874C12Q1/6872
    • Provided is a method for sequencing DNA, which comprises: (a) obtaining a target DNA population comprising one or more single-stranded DNAs to be sequenced, each of which is present in a unique amount and bears a primer to provide a double-stranded portion of the DNA for ligation thereto; (b) contacting the DNA population with an array of hybridisation probes, each probe comprising a label cleavably attached to a known base sequence of predetermined length, the array containing all possible base sequences of that predetermined length; (c) removing all unligated probes; followed by the steps of: (d) cleaving the ligated probes to release each label; (e) recording the quantity of each label; and (f) activating the extended double-stranded portion to enable ligation thereto; wherein (g) steps (b) to (f) are repeated in a cycle for a sufficient number of times to determine the sequence of the or each single-stranded DNA by determining the sequence of release of each label.
    • 提供了一种用于测序DNA的方法,其包括:(a)获得包含待测序的一个或多个单链DNA的靶DNA群体,其中每一个以独特的量存在并承载引物以提供双链 DNA连接部分; (b)使DNA群体与杂交探针阵列接触,每个探针包含与预定长度的已知碱基序列可切割地连接的标记,该阵列包含该预定长度的所有可能的碱基序列; (c)清除所有未连接的探针; 其次是以下步骤:(d)切割连接的探针以释放每个标签; (e)记录每个标签的数量; 和(f)活化延伸的双链部分以使其能够连接; 其中(g)步骤(b)至(f)在循环中重复足够多次,以通过确定每个标记的释放顺序来确定该单链DNA或每个单链DNA的序列。