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TIB MOLBIOL simpleprobe ® probes
Simpleprobe ® Probes, supplied by TIB MOLBIOL, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
simpleprobe ® probes - by Bioz Stars, 2026-03
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TIB MOLBIOL simpleprobe probes for the identification of bartonella genus, b. henselae, and b. quintana dna
Sequences of oligonucleotides relevant to this study
Simpleprobe Probes For The Identification Of Bartonella Genus, B. Henselae, And B. Quintana Dna, supplied by TIB MOLBIOL, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Amplification curves generated when the <t>SimpleProbe®</t> US_NmUC assay was tested against various microorganisms that can colonize the urogenital tract.
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Sequences of oligonucleotides relevant to this study

Journal: Journal of Clinical Microbiology

Article Title: Laboratory Diagnosis of 37 Cases of Bartonella Endocarditis Based on Enzyme Immunoassay and Real-Time PCR

doi: 10.1128/JCM.02217-20

Figure Lengend Snippet: Sequences of oligonucleotides relevant to this study

Article Snippet: The resulting PCR product was detected postamplification using 3 SimpleProbe probes for the identification of Bartonella genus, B. henselae , and B. quintana DNA (TIB MOLBIOL, Berlin, Germany, and Dyn Diagnostics, Migdal HaEmeq, Israel) ( ).

Techniques: Sequencing, Real-time Polymerase Chain Reaction

Multiplex real-time PCR using 3 SimpleProbe probes: Bartonella genus-specific, B. henselae-specific, and B. quintana-specific probes. PCR was performed on valvular tissue of a 65-year-old patient with native aortic valve Bartonella quintana endocarditis (patient number 34 [Table 2]). Two fluorescent peaks corresponding to melting temperatures (Tms) of 57.2°C and 67.6°C are the result of detachment of the genus-specific and B. quintana-specific probes from the PCR product, respectively. Plasmids pMR-ribC185-Bq and pMR-ribC185-Bh were used as positive controls for B. quintana and B. henselae, respectively.

Journal: Journal of Clinical Microbiology

Article Title: Laboratory Diagnosis of 37 Cases of Bartonella Endocarditis Based on Enzyme Immunoassay and Real-Time PCR

doi: 10.1128/JCM.02217-20

Figure Lengend Snippet: Multiplex real-time PCR using 3 SimpleProbe probes: Bartonella genus-specific, B. henselae-specific, and B. quintana-specific probes. PCR was performed on valvular tissue of a 65-year-old patient with native aortic valve Bartonella quintana endocarditis (patient number 34 [Table 2]). Two fluorescent peaks corresponding to melting temperatures (Tms) of 57.2°C and 67.6°C are the result of detachment of the genus-specific and B. quintana-specific probes from the PCR product, respectively. Plasmids pMR-ribC185-Bq and pMR-ribC185-Bh were used as positive controls for B. quintana and B. henselae, respectively.

Article Snippet: The resulting PCR product was detected postamplification using 3 SimpleProbe probes for the identification of Bartonella genus, B. henselae , and B. quintana DNA (TIB MOLBIOL, Berlin, Germany, and Dyn Diagnostics, Migdal HaEmeq, Israel) ( ).

Techniques: Multiplex Assay, Real-time Polymerase Chain Reaction

Multiplex real-time PCR using 2 SimpleProbe probes, B. henselae-specific and genus-specific probes. PCR was performed on valvular tissue of a 56-year-old patient with native mitral valve Bartonella henselae endocarditis (patient number 13 [Table 2]). Two fluorescent peaks corresponding to Tms of 49.3°C and 59.8°C are the result of detachment of the B. henselae-specific and genus-specific probes from the PCR product, respectively. Plasmids pMR-ribC185-Bq and pMR-ribC185-Bh were used as positive controls for B. quintana and B. henselae, respectively. The peak corresponding to the B. quintana-specific probe is not seen since the B. quintana-specific probe was not used in this specific assay.

Journal: Journal of Clinical Microbiology

Article Title: Laboratory Diagnosis of 37 Cases of Bartonella Endocarditis Based on Enzyme Immunoassay and Real-Time PCR

doi: 10.1128/JCM.02217-20

Figure Lengend Snippet: Multiplex real-time PCR using 2 SimpleProbe probes, B. henselae-specific and genus-specific probes. PCR was performed on valvular tissue of a 56-year-old patient with native mitral valve Bartonella henselae endocarditis (patient number 13 [Table 2]). Two fluorescent peaks corresponding to Tms of 49.3°C and 59.8°C are the result of detachment of the B. henselae-specific and genus-specific probes from the PCR product, respectively. Plasmids pMR-ribC185-Bq and pMR-ribC185-Bh were used as positive controls for B. quintana and B. henselae, respectively. The peak corresponding to the B. quintana-specific probe is not seen since the B. quintana-specific probe was not used in this specific assay.

Article Snippet: The resulting PCR product was detected postamplification using 3 SimpleProbe probes for the identification of Bartonella genus, B. henselae , and B. quintana DNA (TIB MOLBIOL, Berlin, Germany, and Dyn Diagnostics, Migdal HaEmeq, Israel) ( ).

Techniques: Multiplex Assay, Real-time Polymerase Chain Reaction

Amplification curves generated when the SimpleProbe® US_NmUC assay was tested against various microorganisms that can colonize the urogenital tract.

Journal: PLoS ONE

Article Title: Development of a SimpleProbe real-Time PCR Assay for rapid detection and identification of the US novel urethrotropic clade of Neisseria meningitidis ST-11 (US_NmUC)

doi: 10.1371/journal.pone.0228467

Figure Lengend Snippet: Amplification curves generated when the SimpleProbe® US_NmUC assay was tested against various microorganisms that can colonize the urogenital tract.

Article Snippet: A SimpleProbe® probe PNM1 ( Fluorescein-SPC-CGTCATCAGCGATACGCG-Phosphate ) was synthesized by FLUORESENTRIC (Park City, UT).

Techniques: Amplification, Generated

Amplification curves generated when the SimpleProbe® US_NmUC assay was tested against various dilutions of NG and NM.

Journal: PLoS ONE

Article Title: Development of a SimpleProbe real-Time PCR Assay for rapid detection and identification of the US novel urethrotropic clade of Neisseria meningitidis ST-11 (US_NmUC)

doi: 10.1371/journal.pone.0228467

Figure Lengend Snippet: Amplification curves generated when the SimpleProbe® US_NmUC assay was tested against various dilutions of NG and NM.

Article Snippet: A SimpleProbe® probe PNM1 ( Fluorescein-SPC-CGTCATCAGCGATACGCG-Phosphate ) was synthesized by FLUORESENTRIC (Park City, UT).

Techniques: Amplification, Generated

Amplification curves generated from specimens of the first 20 men in the IUMP cohort using the SimpleProbe® US_NmUC assay.

Journal: PLoS ONE

Article Title: Development of a SimpleProbe real-Time PCR Assay for rapid detection and identification of the US novel urethrotropic clade of Neisseria meningitidis ST-11 (US_NmUC)

doi: 10.1371/journal.pone.0228467

Figure Lengend Snippet: Amplification curves generated from specimens of the first 20 men in the IUMP cohort using the SimpleProbe® US_NmUC assay.

Article Snippet: A SimpleProbe® probe PNM1 ( Fluorescein-SPC-CGTCATCAGCGATACGCG-Phosphate ) was synthesized by FLUORESENTRIC (Park City, UT).

Techniques: Amplification, Generated