biofire® filmarray® blood culture identification 2 Search Results


actin antibody  (NSJ Bioreagents)
99
NSJ Bioreagents actin antibody
Actin Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
actin antibody - by Bioz Stars, 2026-04
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filmarray blood culture identification 2 panel  (BioFire Defense)
90
BioFire Defense filmarray blood culture identification 2 panel
Filmarray Blood Culture Identification 2 Panel, supplied by BioFire Defense, 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
filmarray blood culture identification 2 panel - by Bioz Stars, 2026-04
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filmarray blood culture identification 2 (bcid2) panel  (BioFire Defense)
90
BioFire Defense filmarray blood culture identification 2 (bcid2) panel
Filmarray Blood Culture Identification 2 (Bcid2) Panel, supplied by BioFire Defense, 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
filmarray blood culture identification 2 (bcid2) panel - by Bioz Stars, 2026-04
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biofire® filmarray® blood culture identification 2 panel  (BioFire Defense)
90
BioFire Defense biofire® filmarray® blood culture identification 2 panel
Biofire® Filmarray® Blood Culture Identification 2 Panel, supplied by BioFire Defense, 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
biofire® filmarray® blood culture identification 2 panel - by Bioz Stars, 2026-04
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filmarray blood culture identification 2 (bcid2) panel  (BioFire Diagnostics)
90
BioFire Diagnostics filmarray blood culture identification 2 (bcid2) panel
Filmarray Blood Culture Identification 2 (Bcid2) Panel, supplied by BioFire Diagnostics, 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
filmarray blood culture identification 2 (bcid2) panel - by Bioz Stars, 2026-04
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protein identification 2 de gels  (Bio-Rad)
96
Bio-Rad protein identification 2 de gels
Protein Identification 2 De Gels, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
protein identification 2 de gels - by Bioz Stars, 2026-04
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blood culture identification 2 panel  (bioMerieux gmbh)
90
bioMerieux gmbh blood culture identification 2 panel
BioFire <t> BCID2 </t> panel; MRSA, methicillin-resistant Staphylococcus aureus .
Blood Culture Identification 2 Panel, supplied by bioMerieux gmbh, 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
blood culture identification 2 panel - by Bioz Stars, 2026-04
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maldi tof ms protein identification 2 d gel electrophoresis spots  (Eppendorf AG)
95
Eppendorf AG maldi tof ms protein identification 2 d gel electrophoresis spots
Figure 2. HCV induces posttranslational modification of β-actin and alteration of its cellular distribution. (A, B) 2-D gel <t>electrophoresis</t> (2-DE) analysis of solubilised membrane protein extracts from (A) replication competent HCV (Jc1 strain) and uninfected Huh7 cells, and (B) replication-deficient HCV (GND-mutant) and HCV (Jc1) cells. In Jc1-infected cells, there was an additional ~40-kD-size protein spot (encircled in red, marked by arrows) identified by <t>MALDI</t> TOF-MS as β-actin. The images shown are representative 2-DE gels from three independent experiments. (C) β-actin and α-tubulin protein levels in cells infected with replication competent (Jc1) or replication-deficient (GND) HCV. A representative Western blot is shown. The black line in the tubulin blot indicates a splice in the blot to present only the GND and Jc1 bands. (D) Increased β-actin filament distribution (denoted by yellow arrows) in Jc1 infected cells compared with uninfected controls. Scale bar represents 15 μm. (E) Measurement of total area of β-actin fluorescence using FIJI. Each column represents the mean measurement from 20 cells in three different experiments. Error bar represent SEM (*P < 0.05). Source data are available for this figure.
Maldi Tof Ms Protein Identification 2 D Gel Electrophoresis Spots, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
maldi tof ms protein identification 2 d gel electrophoresis spots - by Bioz Stars, 2026-04
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multiplex pcr biofirer blood culture identification 2 (bcid2) panel  (bioMerieux gmbh)
90
bioMerieux gmbh multiplex pcr biofirer blood culture identification 2 (bcid2) panel
Figure 2. HCV induces posttranslational modification of β-actin and alteration of its cellular distribution. (A, B) 2-D gel <t>electrophoresis</t> (2-DE) analysis of solubilised membrane protein extracts from (A) replication competent HCV (Jc1 strain) and uninfected Huh7 cells, and (B) replication-deficient HCV (GND-mutant) and HCV (Jc1) cells. In Jc1-infected cells, there was an additional ~40-kD-size protein spot (encircled in red, marked by arrows) identified by <t>MALDI</t> TOF-MS as β-actin. The images shown are representative 2-DE gels from three independent experiments. (C) β-actin and α-tubulin protein levels in cells infected with replication competent (Jc1) or replication-deficient (GND) HCV. A representative Western blot is shown. The black line in the tubulin blot indicates a splice in the blot to present only the GND and Jc1 bands. (D) Increased β-actin filament distribution (denoted by yellow arrows) in Jc1 infected cells compared with uninfected controls. Scale bar represents 15 μm. (E) Measurement of total area of β-actin fluorescence using FIJI. Each column represents the mean measurement from 20 cells in three different experiments. Error bar represent SEM (*P < 0.05). Source data are available for this figure.
Multiplex Pcr Biofirer Blood Culture Identification 2 (Bcid2) Panel, supplied by bioMerieux gmbh, 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
multiplex pcr biofirer blood culture identification 2 (bcid2) panel - by Bioz Stars, 2026-04
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gnathosoma (lateral, dissected)  (Quelle GmbH)
90
Quelle GmbH gnathosoma (lateral, dissected)
Figure 2. HCV induces posttranslational modification of β-actin and alteration of its cellular distribution. (A, B) 2-D gel <t>electrophoresis</t> (2-DE) analysis of solubilised membrane protein extracts from (A) replication competent HCV (Jc1 strain) and uninfected Huh7 cells, and (B) replication-deficient HCV (GND-mutant) and HCV (Jc1) cells. In Jc1-infected cells, there was an additional ~40-kD-size protein spot (encircled in red, marked by arrows) identified by <t>MALDI</t> TOF-MS as β-actin. The images shown are representative 2-DE gels from three independent experiments. (C) β-actin and α-tubulin protein levels in cells infected with replication competent (Jc1) or replication-deficient (GND) HCV. A representative Western blot is shown. The black line in the tubulin blot indicates a splice in the blot to present only the GND and Jc1 bands. (D) Increased β-actin filament distribution (denoted by yellow arrows) in Jc1 infected cells compared with uninfected controls. Scale bar represents 15 μm. (E) Measurement of total area of β-actin fluorescence using FIJI. Each column represents the mean measurement from 20 cells in three different experiments. Error bar represent SEM (*P < 0.05). Source data are available for this figure.
Gnathosoma (Lateral, Dissected), supplied by Quelle GmbH, 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
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2 × paired-end sequencing  (Illumina Inc)
90
Illumina Inc 2 × paired-end sequencing
Figure 2. HCV induces posttranslational modification of β-actin and alteration of its cellular distribution. (A, B) 2-D gel <t>electrophoresis</t> (2-DE) analysis of solubilised membrane protein extracts from (A) replication competent HCV (Jc1 strain) and uninfected Huh7 cells, and (B) replication-deficient HCV (GND-mutant) and HCV (Jc1) cells. In Jc1-infected cells, there was an additional ~40-kD-size protein spot (encircled in red, marked by arrows) identified by <t>MALDI</t> TOF-MS as β-actin. The images shown are representative 2-DE gels from three independent experiments. (C) β-actin and α-tubulin protein levels in cells infected with replication competent (Jc1) or replication-deficient (GND) HCV. A representative Western blot is shown. The black line in the tubulin blot indicates a splice in the blot to present only the GND and Jc1 bands. (D) Increased β-actin filament distribution (denoted by yellow arrows) in Jc1 infected cells compared with uninfected controls. Scale bar represents 15 μm. (E) Measurement of total area of β-actin fluorescence using FIJI. Each column represents the mean measurement from 20 cells in three different experiments. Error bar represent SEM (*P < 0.05). Source data are available for this figure.
2 × Paired End Sequencing, supplied by Illumina 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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Average 90 stars, based on 1 article reviews
2 × paired-end sequencing - by Bioz Stars, 2026-04
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ltq-orbitrap mass spectrometer  (Thermo Fisher)
90
Thermo Fisher ltq-orbitrap mass spectrometer
Figure 2. HCV induces posttranslational modification of β-actin and alteration of its cellular distribution. (A, B) 2-D gel <t>electrophoresis</t> (2-DE) analysis of solubilised membrane protein extracts from (A) replication competent HCV (Jc1 strain) and uninfected Huh7 cells, and (B) replication-deficient HCV (GND-mutant) and HCV (Jc1) cells. In Jc1-infected cells, there was an additional ~40-kD-size protein spot (encircled in red, marked by arrows) identified by <t>MALDI</t> TOF-MS as β-actin. The images shown are representative 2-DE gels from three independent experiments. (C) β-actin and α-tubulin protein levels in cells infected with replication competent (Jc1) or replication-deficient (GND) HCV. A representative Western blot is shown. The black line in the tubulin blot indicates a splice in the blot to present only the GND and Jc1 bands. (D) Increased β-actin filament distribution (denoted by yellow arrows) in Jc1 infected cells compared with uninfected controls. Scale bar represents 15 μm. (E) Measurement of total area of β-actin fluorescence using FIJI. Each column represents the mean measurement from 20 cells in three different experiments. Error bar represent SEM (*P < 0.05). Source data are available for this figure.
Ltq Orbitrap Mass Spectrometer, supplied by Thermo Fisher, 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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Image Search Results


BioFire BCID2 panel; MRSA, methicillin-resistant Staphylococcus aureus .

Journal: Heliyon

Article Title: Performance of the BioFire Blood Culture Identification 2 panel for the diagnosis of bloodstream infections

doi: 10.1016/j.heliyon.2022.e09983

Figure Lengend Snippet: BioFire BCID2 panel; MRSA, methicillin-resistant Staphylococcus aureus .

Article Snippet: A new version of this assay has been recently released (BioFire Blood Culture Identification 2 Panel, bioMerieux, France) resulting in a broader panel including 33 pathogens (26 bacterial genera/species and 7 fungal species) and 10 resistance markers; few studies have evaluated the performance of BCID2 on clinical samples so far [ , , , , ].

Techniques:

Performance characteristics of the BCID2 compared to conventional culture shown for each target for monomicrobial samples.

Journal: Heliyon

Article Title: Performance of the BioFire Blood Culture Identification 2 panel for the diagnosis of bloodstream infections

doi: 10.1016/j.heliyon.2022.e09983

Figure Lengend Snippet: Performance characteristics of the BCID2 compared to conventional culture shown for each target for monomicrobial samples.

Article Snippet: A new version of this assay has been recently released (BioFire Blood Culture Identification 2 Panel, bioMerieux, France) resulting in a broader panel including 33 pathogens (26 bacterial genera/species and 7 fungal species) and 10 resistance markers; few studies have evaluated the performance of BCID2 on clinical samples so far [ , , , , ].

Techniques:

Concordance between BCID2 and traditional methods for polymicrobial blood cultures.

Journal: Heliyon

Article Title: Performance of the BioFire Blood Culture Identification 2 panel for the diagnosis of bloodstream infections

doi: 10.1016/j.heliyon.2022.e09983

Figure Lengend Snippet: Concordance between BCID2 and traditional methods for polymicrobial blood cultures.

Article Snippet: A new version of this assay has been recently released (BioFire Blood Culture Identification 2 Panel, bioMerieux, France) resulting in a broader panel including 33 pathogens (26 bacterial genera/species and 7 fungal species) and 10 resistance markers; few studies have evaluated the performance of BCID2 on clinical samples so far [ , , , , ].

Techniques:

Resistance markers detected by BCID2 and in-house PCR and correlation to bacterial phenotype.

Journal: Heliyon

Article Title: Performance of the BioFire Blood Culture Identification 2 panel for the diagnosis of bloodstream infections

doi: 10.1016/j.heliyon.2022.e09983

Figure Lengend Snippet: Resistance markers detected by BCID2 and in-house PCR and correlation to bacterial phenotype.

Article Snippet: A new version of this assay has been recently released (BioFire Blood Culture Identification 2 Panel, bioMerieux, France) resulting in a broader panel including 33 pathogens (26 bacterial genera/species and 7 fungal species) and 10 resistance markers; few studies have evaluated the performance of BCID2 on clinical samples so far [ , , , , ].

Techniques:

Figure 2. HCV induces posttranslational modification of β-actin and alteration of its cellular distribution. (A, B) 2-D gel electrophoresis (2-DE) analysis of solubilised membrane protein extracts from (A) replication competent HCV (Jc1 strain) and uninfected Huh7 cells, and (B) replication-deficient HCV (GND-mutant) and HCV (Jc1) cells. In Jc1-infected cells, there was an additional ~40-kD-size protein spot (encircled in red, marked by arrows) identified by MALDI TOF-MS as β-actin. The images shown are representative 2-DE gels from three independent experiments. (C) β-actin and α-tubulin protein levels in cells infected with replication competent (Jc1) or replication-deficient (GND) HCV. A representative Western blot is shown. The black line in the tubulin blot indicates a splice in the blot to present only the GND and Jc1 bands. (D) Increased β-actin filament distribution (denoted by yellow arrows) in Jc1 infected cells compared with uninfected controls. Scale bar represents 15 μm. (E) Measurement of total area of β-actin fluorescence using FIJI. Each column represents the mean measurement from 20 cells in three different experiments. Error bar represent SEM (*P < 0.05). Source data are available for this figure.

Journal: Life science alliance

Article Title: Polo-like kinase-1 mediates hepatitis C virus-induced cell migration, a drug target for liver cancer.

doi: 10.26508/lsa.202201630

Figure Lengend Snippet: Figure 2. HCV induces posttranslational modification of β-actin and alteration of its cellular distribution. (A, B) 2-D gel electrophoresis (2-DE) analysis of solubilised membrane protein extracts from (A) replication competent HCV (Jc1 strain) and uninfected Huh7 cells, and (B) replication-deficient HCV (GND-mutant) and HCV (Jc1) cells. In Jc1-infected cells, there was an additional ~40-kD-size protein spot (encircled in red, marked by arrows) identified by MALDI TOF-MS as β-actin. The images shown are representative 2-DE gels from three independent experiments. (C) β-actin and α-tubulin protein levels in cells infected with replication competent (Jc1) or replication-deficient (GND) HCV. A representative Western blot is shown. The black line in the tubulin blot indicates a splice in the blot to present only the GND and Jc1 bands. (D) Increased β-actin filament distribution (denoted by yellow arrows) in Jc1 infected cells compared with uninfected controls. Scale bar represents 15 μm. (E) Measurement of total area of β-actin fluorescence using FIJI. Each column represents the mean measurement from 20 cells in three different experiments. Error bar represent SEM (*P < 0.05). Source data are available for this figure.

Article Snippet: MALDI TOF-MS protein identification 2-D gel electrophoresis spots of interest were excised and transferred into 1.5 ml sterile LoBind tubes (Eppendorf) for in-gel protein digestion.

Techniques: Nucleic Acid Electrophoresis, Membrane, Mutagenesis, Infection, Western Blot