real time quantitative fluorescence polymerase chain reaction Search Results


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Shanghai Fosun Long March Medical Science fluorescent quantitative polymerase chain reaction (qpcr) technique
Fluorescent Quantitative Polymerase Chain Reaction (Qpcr) Technique, supplied by Shanghai Fosun Long March Medical Science, 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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tiangen biotech co reverse transcription-fluorescence quantitative polymerase chain reaction (qpcr) kit
Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative <t>polymerase</t> chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.
Reverse Transcription Fluorescence Quantitative Polymerase Chain Reaction (Qpcr) Kit, supplied by tiangen biotech co, 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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Shanghai Kehua quantitative fluorescence polymerase chain reaction (pcr)
Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative <t>polymerase</t> chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.
Quantitative Fluorescence Polymerase Chain Reaction (Pcr), supplied by Shanghai Kehua, 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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PrimerDesign Inc fluorescence quantitative reverse transcription polymerase chain reaction (qrt-pcr)
Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative <t>polymerase</t> chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.
Fluorescence Quantitative Reverse Transcription Polymerase Chain Reaction (Qrt Pcr), supplied by PrimerDesign Inc, 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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Sangong Corporation fluorescence quantitative polymerase chain reaction (pcr) kit
Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative <t>polymerase</t> chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.
Fluorescence Quantitative Polymerase Chain Reaction (Pcr) Kit, supplied by Sangong Corporation, 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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Sansure Biotech Inc real time fluorescence quantitative polymerase chain reaction assays
Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative <t>polymerase</t> chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.
Real Time Fluorescence Quantitative Polymerase Chain Reaction Assays, supplied by Sansure Biotech Inc, 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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Shanghai Fosun Pharmaceutical slan-96s fluorescence quantitative polymerase chain reaction (pcr) instrument
Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative <t>polymerase</t> chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.
Slan 96s Fluorescence Quantitative Polymerase Chain Reaction (Pcr) Instrument, supplied by Shanghai Fosun Pharmaceutical, 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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Aikang MedTech real-time fluorescent quantitative polymerase chain reaction (rt–pcr)
Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative <t>polymerase</t> chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.
Real Time Fluorescent Quantitative Polymerase Chain Reaction (Rt–Pcr), supplied by Aikang MedTech, 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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Acon Biotech Hangzhou Co Ltd hbv dna fluorescence quantitative detection reagent kit
Distribution of HBsAg-positive prevalence in all 45,256 individuals and in 2,544 HBsAg-positive subjects.
Hbv Dna Fluorescence Quantitative Detection Reagent Kit, supplied by Acon Biotech Hangzhou Co Ltd, 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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Eppendorf AG sybr green i fluorescent quantitative polymerase chain reaction (pcr)
Distribution of HBsAg-positive prevalence in all 45,256 individuals and in 2,544 HBsAg-positive subjects.
Sybr Green I Fluorescent Quantitative Polymerase Chain Reaction (Pcr), supplied by Eppendorf AG, 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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tiangen biotech co fluorescence quantitative polymerase chain reaction (pcr) reagents
Distribution of HBsAg-positive prevalence in all 45,256 individuals and in 2,544 HBsAg-positive subjects.
Fluorescence Quantitative Polymerase Chain Reaction (Pcr) Reagents, supplied by tiangen biotech co, 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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Novoprotein fluorescence quantitative polymerase chain reaction (pcr) detection kit 0513471
Distribution of HBsAg-positive prevalence in all 45,256 individuals and in 2,544 HBsAg-positive subjects.
Fluorescence Quantitative Polymerase Chain Reaction (Pcr) Detection Kit 0513471, supplied by Novoprotein, 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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Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative polymerase chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.

Journal: World Journal of Stem Cells

Article Title: MicroRNA-584-5p/RUNX family transcription factor 2 axis mediates hypoxia-induced osteogenic differentiation of periosteal stem cells

doi: 10.4252/wjsc.v15.i10.979

Figure Lengend Snippet: Prediction of the miRNA-584-5p target. A: Potential binding sites of miRNA-584-5p and the 3’-untranslated region of RUNX family transcription factor 2 (RUNX2); B: Dual luciferase reporter gene assay; C: Quantitative polymerase chain reaction determination of RUNX2 expression; D: Western blot determination of RUNX2 protein expression. One-way ANOVA and t tests were used to demonstrate differences in RUNX2 responses between the miR584-5p mimic and negative control groups. a P < 0.05; b P < 0.01. RUNX2: RUNX family transcription factor 2; NC: Negative control; wt: Wild type; mut: Mutant; miRNA: MicroRNA.

Article Snippet: RNA was reverse-transcribed into cDNA using a reverse transcription-fluorescence quantitative polymerase chain reaction (qPCR) kit (Tiangen, Beijing, China) and PCR apparatus (Applied Biosystems, United States) for real-time fluorescence quantification (qPCR) after determining the purity of the RNA samples.

Techniques: Binding Assay, Luciferase, Reporter Gene Assay, Real-time Polymerase Chain Reaction, Expressing, Western Blot, Negative Control, Mutagenesis

Distribution of HBsAg-positive prevalence in all 45,256 individuals and in 2,544 HBsAg-positive subjects.

Journal: Experimental and Therapeutic Medicine

Article Title: Clinical characteristics and association analysis of persistent low-level HBsAg expression in a physical examination population with HBV infection

doi: 10.3892/etm.2019.8217

Figure Lengend Snippet: Distribution of HBsAg-positive prevalence in all 45,256 individuals and in 2,544 HBsAg-positive subjects.

Article Snippet: A total of 100 μl of eluent (i.e., HBV DNA extract) was collected for real-time quantitative fluorometric detection of HBV DNA, according to the manufacturer's protocol of HBV DNA fluorescence quantitative detection reagent kit [ACON Biotech (Hangzhou) co., Ltd.] and an ABI StepOnePlusTM real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.).

Techniques:

Clinical laboratory parameters of 2,544 HBsAg-positive subjects with  HBV  infection.

Journal: Experimental and Therapeutic Medicine

Article Title: Clinical characteristics and association analysis of persistent low-level HBsAg expression in a physical examination population with HBV infection

doi: 10.3892/etm.2019.8217

Figure Lengend Snippet: Clinical laboratory parameters of 2,544 HBsAg-positive subjects with HBV infection.

Article Snippet: A total of 100 μl of eluent (i.e., HBV DNA extract) was collected for real-time quantitative fluorometric detection of HBV DNA, according to the manufacturer's protocol of HBV DNA fluorescence quantitative detection reagent kit [ACON Biotech (Hangzhou) co., Ltd.] and an ABI StepOnePlusTM real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.).

Techniques: Infection

Distribution of the prevalence of different level HBsAg positivity and HBV DNA positivity in HBsAg-level groups according to age in a physical examination population. (A) Prevalence of HBsAg positivity in the low-level HBsAg group according to age in a physical examination population. (B) Prevalence of different levels of HBsAg positivity in the high-level HBsAg groups (≥10-100, ≥100–200 or ≥200 IU/ml and total group) according to age in a physical examination population. P<0.05, ≥10–100 IU/ml group vs. ≥100–200 group, ≥10–100 IU/ml group vs. ≥200 IU/ml group and ≥10–100 IU/ml group vs. ≥200 IU/ml group. (C) Prevalence of HBV DNA positivity in the low-level HBsAg group according to age in a physical examination population. P<0.05, enrichment method group vs. routine method group. (D) Prevalence of HBV DNA positivity in the high-level HBsAg group (≥10-100, ≥100–200 or ≥200 IU/ml, and total group) according to age in a physical examination population. P<0.05, ≥10–100 IU/ml group vs. ≥100–200 group, ≥10–100 IU/ml group vs. ≥200 IU/ml group and ≥10–100 IU/ml group vs. ≥200 IU/ml group. HBV, hepatitis B virus; HBsAg, hepatitis B surface antigen; y, years.

Journal: Experimental and Therapeutic Medicine

Article Title: Clinical characteristics and association analysis of persistent low-level HBsAg expression in a physical examination population with HBV infection

doi: 10.3892/etm.2019.8217

Figure Lengend Snippet: Distribution of the prevalence of different level HBsAg positivity and HBV DNA positivity in HBsAg-level groups according to age in a physical examination population. (A) Prevalence of HBsAg positivity in the low-level HBsAg group according to age in a physical examination population. (B) Prevalence of different levels of HBsAg positivity in the high-level HBsAg groups (≥10-100, ≥100–200 or ≥200 IU/ml and total group) according to age in a physical examination population. P<0.05, ≥10–100 IU/ml group vs. ≥100–200 group, ≥10–100 IU/ml group vs. ≥200 IU/ml group and ≥10–100 IU/ml group vs. ≥200 IU/ml group. (C) Prevalence of HBV DNA positivity in the low-level HBsAg group according to age in a physical examination population. P<0.05, enrichment method group vs. routine method group. (D) Prevalence of HBV DNA positivity in the high-level HBsAg group (≥10-100, ≥100–200 or ≥200 IU/ml, and total group) according to age in a physical examination population. P<0.05, ≥10–100 IU/ml group vs. ≥100–200 group, ≥10–100 IU/ml group vs. ≥200 IU/ml group and ≥10–100 IU/ml group vs. ≥200 IU/ml group. HBV, hepatitis B virus; HBsAg, hepatitis B surface antigen; y, years.

Article Snippet: A total of 100 μl of eluent (i.e., HBV DNA extract) was collected for real-time quantitative fluorometric detection of HBV DNA, according to the manufacturer's protocol of HBV DNA fluorescence quantitative detection reagent kit [ACON Biotech (Hangzhou) co., Ltd.] and an ABI StepOnePlusTM real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.).

Techniques: Virus

Distribution of serological patterns and clinical types in 2,544 subjects with chronic  HBV  infection in two groups.

Journal: Experimental and Therapeutic Medicine

Article Title: Clinical characteristics and association analysis of persistent low-level HBsAg expression in a physical examination population with HBV infection

doi: 10.3892/etm.2019.8217

Figure Lengend Snippet: Distribution of serological patterns and clinical types in 2,544 subjects with chronic HBV infection in two groups.

Article Snippet: A total of 100 μl of eluent (i.e., HBV DNA extract) was collected for real-time quantitative fluorometric detection of HBV DNA, according to the manufacturer's protocol of HBV DNA fluorescence quantitative detection reagent kit [ACON Biotech (Hangzhou) co., Ltd.] and an ABI StepOnePlusTM real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.).

Techniques: Infection

 HBV DNA  and HBV markers for major serological patterns and clinical types in the two groups <xref ref-type= a ." width="100%" height="100%">

Journal: Experimental and Therapeutic Medicine

Article Title: Clinical characteristics and association analysis of persistent low-level HBsAg expression in a physical examination population with HBV infection

doi: 10.3892/etm.2019.8217

Figure Lengend Snippet: HBV DNA and HBV markers for major serological patterns and clinical types in the two groups a .

Article Snippet: A total of 100 μl of eluent (i.e., HBV DNA extract) was collected for real-time quantitative fluorometric detection of HBV DNA, according to the manufacturer's protocol of HBV DNA fluorescence quantitative detection reagent kit [ACON Biotech (Hangzhou) co., Ltd.] and an ABI StepOnePlusTM real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.).

Techniques:

Analysis of the association of  HBV DNA  with age and HBV markers of the serological pattern  HBV-M2  <xref ref-type= a , b ." width="100%" height="100%">

Journal: Experimental and Therapeutic Medicine

Article Title: Clinical characteristics and association analysis of persistent low-level HBsAg expression in a physical examination population with HBV infection

doi: 10.3892/etm.2019.8217

Figure Lengend Snippet: Analysis of the association of HBV DNA with age and HBV markers of the serological pattern HBV-M2 a , b .

Article Snippet: A total of 100 μl of eluent (i.e., HBV DNA extract) was collected for real-time quantitative fluorometric detection of HBV DNA, according to the manufacturer's protocol of HBV DNA fluorescence quantitative detection reagent kit [ACON Biotech (Hangzhou) co., Ltd.] and an ABI StepOnePlusTM real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.).

Techniques:

Clinical laboratory parameters for ASC patients.

Journal: Experimental and Therapeutic Medicine

Article Title: Clinical characteristics and association analysis of persistent low-level HBsAg expression in a physical examination population with HBV infection

doi: 10.3892/etm.2019.8217

Figure Lengend Snippet: Clinical laboratory parameters for ASC patients.

Article Snippet: A total of 100 μl of eluent (i.e., HBV DNA extract) was collected for real-time quantitative fluorometric detection of HBV DNA, according to the manufacturer's protocol of HBV DNA fluorescence quantitative detection reagent kit [ACON Biotech (Hangzhou) co., Ltd.] and an ABI StepOnePlusTM real-time PCR system (Applied Biosystems; Thermo Fisher Scientific, Inc.).

Techniques: