MX2022003615A - Specific synthetic oligonucleotides for the detection of the genetic material of rickettsia rickettsii and its detection method. - Google Patents
Specific synthetic oligonucleotides for the detection of the genetic material of rickettsia rickettsii and its detection method.Info
- Publication number
- MX2022003615A MX2022003615A MX2022003615A MX2022003615A MX2022003615A MX 2022003615 A MX2022003615 A MX 2022003615A MX 2022003615 A MX2022003615 A MX 2022003615A MX 2022003615 A MX2022003615 A MX 2022003615A MX 2022003615 A MX2022003615 A MX 2022003615A
- Authority
- MX
- Mexico
- Prior art keywords
- detection
- rickettsia rickettsii
- genetic material
- synthetic oligonucleotides
- specific synthetic
- Prior art date
Links
- 108091034117 Oligonucleotide Proteins 0.000 title abstract 3
- 241000606695 Rickettsia rickettsii Species 0.000 title abstract 3
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 title abstract 3
- 238000001514 detection method Methods 0.000 title abstract 3
- 229940075118 rickettsia rickettsii Drugs 0.000 title abstract 3
- 102000004169 proteins and genes Human genes 0.000 title 1
- 108090000623 proteins and genes Proteins 0.000 title 1
- 238000000034 method Methods 0.000 abstract 2
- 238000003752 polymerase chain reaction Methods 0.000 abstract 2
- 230000003321 amplification Effects 0.000 abstract 1
- 238000003745 diagnosis Methods 0.000 abstract 1
- 238000011901 isothermal amplification Methods 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 238000003199 nucleic acid amplification method Methods 0.000 abstract 1
- 238000010561 standard procedure Methods 0.000 abstract 1
Landscapes
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
The present invention relates to the unique design of oligonucleotides that specifically hybridize to a Rickettsia rickettsii sequence. The process consists of hybridizing or binding said oligonucleotides to the Rickettsia rickettsii sequence to perform amplification specifically using standard techniques, such as Polymerase Chain Reaction (PCR) or hairpin-based isothermal amplification (LAMP) and its variants in real time as methods of diagnosis or detection of microorganisms.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MX2022003615A MX2022003615A (en) | 2022-03-24 | 2022-03-24 | Specific synthetic oligonucleotides for the detection of the genetic material of rickettsia rickettsii and its detection method. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MX2022003615A MX2022003615A (en) | 2022-03-24 | 2022-03-24 | Specific synthetic oligonucleotides for the detection of the genetic material of rickettsia rickettsii and its detection method. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2022003615A true MX2022003615A (en) | 2023-09-25 |
Family
ID=91023320
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2022003615A MX2022003615A (en) | 2022-03-24 | 2022-03-24 | Specific synthetic oligonucleotides for the detection of the genetic material of rickettsia rickettsii and its detection method. |
Country Status (1)
| Country | Link |
|---|---|
| MX (1) | MX2022003615A (en) |
-
2022
- 2022-03-24 MX MX2022003615A patent/MX2022003615A/en unknown
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