发明名称 |
Rapid detection of mycobacteria |
摘要 |
The invention provides a method for detecting a mycobacterium belonging to the Mycobacterium tuberculosis complex (MTBc) in a sample, the method comprising: (a) contacting the sample with a forward oligonucleotide primer and a reverse oligonucleotide primer; wherein the forward primer hybridizes to a target nucleic acid sequence located within a Mycobacterial Interspersed Repetitive Unit (MIRU) repeat element; and wherein the reverse primer hybridizes to a target nucleic acid sequence located within a MIRU repeat element; (b) extending the forward and reverse primers to generate an amplification product; and (c) detecting the amplification product. |
申请公布号 |
US9150930(B2) |
申请公布日期 |
2015.10.06 |
申请号 |
US200912937263 |
申请日期 |
2009.04.09 |
申请人 |
The Secretary of State for Health |
发明人 |
Arnold Catherine |
分类号 |
C12Q1/68 |
主分类号 |
C12Q1/68 |
代理机构 |
Baker & Hostetler LLP |
代理人 |
Baker & Hostetler LLP |
主权项 |
1. A method for detecting nucleic acid of a mycobacterium belonging to the Mycobacterium tuberculosis (MTBc) in a sample, the method comprising:
(a) contacting the sample with a pair of primers comprising a forward oligonucleotide primer and a reverse oligonucleotide primer, wherein said forward primer hybridizes to a target nucleic acid sequence that is located within multiple Mycobacterial Interspersed Repetitive Unit (MIRU) repeat elements, and wherein said reverse primer hybridizes to a target nucleic acid sequence that is located within the multiple MIRU repeat elements; wherein the forward primer comprises a sequence that is at least 95% identical to a nucleotide sequence selected from SEQ ID NOs: 25-39; and wherein the reverse primer comprises a sequence that is at least 95% identical to the complement of a nucleotide sequence selected from SEQ ID NOs: 40-46; (b) extending said forward and reverse primers to generate at least one amplification product; and (c) detecting the at least one amplification product. |
地址 |
London GB |