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Bruker Corporation outer diameter samplejet nmr tubes
Outer Diameter Samplejet Nmr Tubes, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 97/100, based on 919 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/samplejet+nmr+tubes/SampleJet/pm41780928-26-22-39
Average 97 stars, based on 919 article reviews
outer diameter samplejet nmr tubes - by Bioz Stars, 2026-10
97/100 stars

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Nuclear Magnetic Resonance:

Article Title: Discovery of first-in-class inhibitors of the TRF1:TIN2 protein:protein interaction by fragment screening.
Article Snippet: Solutions were transferred to 1.7-mm NMR tubes using a Bruker SamplePro Tube robotics system. .. 1H NMR spectra were recorded on a Bruker AVIII 500 MHz spectrometer at 298 K, equipped with a 1.7-mm TXI probe, with samples in 1.7-mm SampleJET NMR tubes (Bruker). .. Solutions were transferred to 1.7-mm NMR tubes using a Bruker SamplePro Tube robotics system.

Article Title: Using experimental design and 13 C satellites to optimize the measurement of the absolute concentration of ethanol in wine by 1 H NMR spectroscopy.
Article Snippet: .. SampleJet NMR tubes (Bruker BioSpin, Ettlingen, Germany), which according to the manufacturer, are designed with minimal adsorptive properties. ..

Article Title: Comparative 1 H NMR Metabolomics Between Scandinavian Propolis and Australian Propolis: The Quest to Identify Radical Scavenging Compounds.
Article Snippet: The mixture was vortexed (Buch and Holm, Scientific Industries Vortex- Genie 2) at a medium speed to avoid foaming for 5 min. .. Subsequently, 600 μL of the mixture was transferred into SampleJet NMR tubes (Bruker BioSpin, Ettlingen, Germany) of L = 103.5 mm and O.D. ..

Article Title: Comparative 1 H NMR Metabolomics Between Scandinavian Propolis and Australian Propolis: The Quest to Identify Radical Scavenging Compounds
Article Snippet: The mixture was vortexed (Buch and Holm, Scientific Industries Vortex‐Genie 2) at a medium speed to avoid foaming for 5 min. .. Subsequently, 600 μL of the mixture was transferred into SampleJet NMR tubes (Bruker BioSpin, Ettlingen, Germany) of L = 103.5 mm and O.D. ..

Article Title: Comparison of Lipid Measurements by Clinical Chemistry and NMR Spectroscopy
Article Snippet: For NMR analysis of fresh serum samples, 400 μL of serum was mixed with 400 μL of plasma buffer containing 20% deuterium oxide, 0.075 M sodium monophosphate, 4.6 mM sodium 3-(trimethylsilyl)-2,2,3,3-tetradeuteropropionate (TSP), and 0.04% NaN 3 (Bruker BioSpin GmbH, Ettlingen, Germany). .. The mixture was transferred into 5 mm SampleJet NMR tubes (Bruker BioSpin, Ettlingen, Germany) [ ]. .. Lipid profiles were automatically analyzed using the commercial Bruker IVDr Lipoprotein Subclass Analysis (B.I.LISA) method (Bruker BioSpin) [ ].

Article Title: Discovery of first-in-class inhibitors of the TRF1:TIN2 protein:protein interaction by fragment screening
Article Snippet: Solutions were transferred to 1.7-mm NMR tubes using a Bruker SamplePro Tube robotics system. .. 1 H NMR spectra were recorded on a Bruker AVIII 500 MHz spectrometer at 298 K, equipped with a 1.7-mm TXI probe, with samples in 1.7-mm SampleJET NMR tubes (Bruker). ..

Article Title: Urinary Hippuric Acid as a Sex-Dependent Biomarker for Fruit and Nut Intake Raised from the EAT-Lancet Index and Nuclear Magnetic Resonance Analysis
Article Snippet: .. Following centrifugation (1800× g , 4 °C, 5 min) to remove solids, 550 μL of the sample was transferred into 5 mm SampleJet NMR tubes and immediately loaded onto a refrigerated SampleJet robot (Bruker Biospin, Rheinstetten, Germany) and maintained at 4 °C until NMR analysis. ..

Centrifugation:

Article Title: Urinary Hippuric Acid as a Sex-Dependent Biomarker for Fruit and Nut Intake Raised from the EAT-Lancet Index and Nuclear Magnetic Resonance Analysis
Article Snippet: .. Following centrifugation (1800× g , 4 °C, 5 min) to remove solids, 550 μL of the sample was transferred into 5 mm SampleJet NMR tubes and immediately loaded onto a refrigerated SampleJet robot (Bruker Biospin, Rheinstetten, Germany) and maintained at 4 °C until NMR analysis. ..

other:

Article Title: PFOA induced metabolic and immune perturbations in a SARS-2 infection model
Article Snippet: Whole blood was collected from each ferret using a 3.5 mL CAT Serum Separator Clot Activator Vacuette (Greiner Bio-One, Ref 45228P).



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Bruker Corporation outer diameter samplejet nmr tubes
Outer Diameter Samplejet Nmr Tubes, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/samplejet+nmr+tubes/SampleJet/pm41780928-26-22-39
Average 97 stars, based on 1 article reviews
outer diameter samplejet nmr tubes - by Bioz Stars, 2026-10
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Bruker Corporation samplejet compatible nmr spectroscopy tubes
( a-b ) Metabolic flux analysis ( a ) for extracellular acidification rates (ECAR) of FL83B WT (n = 3) or FL83B TG (n = 3) hepatocytes, with quantification ( b ) for glycolysis and glycolytic capacity. ( c ) Glucose consumption in FL83B WT or FL83B TG hepatocytes cultured for 48 h (n = 6/group). ( d ) qRT-PCR analysis of glucose-related metabolic genes in FL83B WT or FL83B TG cells (n = 6/group). Bold labelling depicts significant genes. ( e ) <t>NMR</t> <t>spectroscopy-based</t> metabolomics analysis of lactate concentration in FL83B cells with ATF6α expression (FL83B TG ) or deletion (FL83B KO ), normalized to respective controls (n = 6/group). ( f ) NMR metabolomics PLS − DA with coloured 95% confidence intervals illustrating the clear group separation in metabolic profile between FL83B WT and FL83B TG cells (n = 6/group). ( g ) qRT-PCR analysis of primary hepatocytes harvested from livers of 3-month-old TG Alb-cre− (n = 4) and TG Alb-cre+ (n = 6) mice. Bold labelling depicts significant genes. ( h ) qRT-PCR analysis of primary hepatocytes harvested from livers of CD-HFD-fed Atf6 fl/fl (n = 6) and Atf6 ΔHep (n = 6) mice. Bold labelling depicts significant genes. ( i ) Scheme of HCC cancer cell line (HLE) stably transfected with control vector (HLE WT ) or nATF6α-expressing (HLE TG ) plasmid and co-cultured with or without cytotoxic MART-1 T-cells to assess immune attack by a real-time cell analyzer (xCELLigence). ( j ) HLE WT or HLE TG cancer cell growth over time with quantification on the right panel (n = 3/group). ( k ) Killing assay and quantification for HLE WT or HLE TG cancer cell growth in co-culture conditions with cytotoxic MART-1 T-cells (n = 3/group). ( l ) Scheme of Colo800 tumour cells stably transfected with control (Colo800 WT ) or nATF6α-expressing (Colo800 TG ) plasmid and co-cultured with cytotoxic MART-1-specific T-cells to assess immune attack in a real-time cell analyzer (xCELLigence). ( m ) Killing assay of Colo800 WT or Colo800 TG tumour cells in co-culture conditions with cytotoxic MART-1-specific T-cells (n = 3/group) in the presence or absence of the lactate dehydrogenase inhibitor galloflavin. ( n ) Killing assay for Colo800 WT or Colo800 TG tumour cell growth in co-culture conditions with cytotoxic MART-1 T-cells (n = 4/group) in the presence or absence of the lactate efflux inhibitor AZD3965. ( o ) Glucose consumption of Colo800 WT and Colo800 TG cells cultured for 48 h (n = 6/group). ( p ) qRT-PCR analysis of indicated mRNAs from Colo800 WT and Colo800 TG cells (n = 6/group). Bold labelling depicts significant genes. ( q ) NMR metabolomics PLS − DA with coloured 95% confidence intervals illustrating the clear group separation in metabolic profile between Colo800 WT (n = 5) and Colo800 TG (n = 6) cells. ( r ) Top 15 metabolites and their VIP score based on the PLS − DA regression model. Scatter dot plot data are presented as mean values ± SEM. Line graph data are presented as mean values ± SEM (10a) or mean values ± SD (10j-k, m-n). Data in 10b-d,g,h,o,p were analysed by two-tailed unpaired t -test or Mann-Whitney test based on data normality distribution. Data in 10e were analysed by one-way ANOVA. Data in 10j,k were calculated for the area under the curve and analysed by two-tailed Student’s t -test. Data in 10m,n were calculated for the area under the curve and analysed by one-way ANOVA. In vitro co-culture schematics were created in BioRender. Heikenwälder, M. (2026) https://BioRender.com/lgjnsy9 .
Samplejet Compatible Nmr Spectroscopy Tubes, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/samplejet+nmr+tubes/SampleJet/pmc12999494-371-8-7
Average 97 stars, based on 1 article reviews
samplejet compatible nmr spectroscopy tubes - by Bioz Stars, 2026-10
97/100 stars
  Buy from Supplier

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( a-b ) Metabolic flux analysis ( a ) for extracellular acidification rates (ECAR) of FL83B WT (n = 3) or FL83B TG (n = 3) hepatocytes, with quantification ( b ) for glycolysis and glycolytic capacity. ( c ) Glucose consumption in FL83B WT or FL83B TG hepatocytes cultured for 48 h (n = 6/group). ( d ) qRT-PCR analysis of glucose-related metabolic genes in FL83B WT or FL83B TG cells (n = 6/group). Bold labelling depicts significant genes. ( e ) NMR spectroscopy-based metabolomics analysis of lactate concentration in FL83B cells with ATF6α expression (FL83B TG ) or deletion (FL83B KO ), normalized to respective controls (n = 6/group). ( f ) NMR metabolomics PLS − DA with coloured 95% confidence intervals illustrating the clear group separation in metabolic profile between FL83B WT and FL83B TG cells (n = 6/group). ( g ) qRT-PCR analysis of primary hepatocytes harvested from livers of 3-month-old TG Alb-cre− (n = 4) and TG Alb-cre+ (n = 6) mice. Bold labelling depicts significant genes. ( h ) qRT-PCR analysis of primary hepatocytes harvested from livers of CD-HFD-fed Atf6 fl/fl (n = 6) and Atf6 ΔHep (n = 6) mice. Bold labelling depicts significant genes. ( i ) Scheme of HCC cancer cell line (HLE) stably transfected with control vector (HLE WT ) or nATF6α-expressing (HLE TG ) plasmid and co-cultured with or without cytotoxic MART-1 T-cells to assess immune attack by a real-time cell analyzer (xCELLigence). ( j ) HLE WT or HLE TG cancer cell growth over time with quantification on the right panel (n = 3/group). ( k ) Killing assay and quantification for HLE WT or HLE TG cancer cell growth in co-culture conditions with cytotoxic MART-1 T-cells (n = 3/group). ( l ) Scheme of Colo800 tumour cells stably transfected with control (Colo800 WT ) or nATF6α-expressing (Colo800 TG ) plasmid and co-cultured with cytotoxic MART-1-specific T-cells to assess immune attack in a real-time cell analyzer (xCELLigence). ( m ) Killing assay of Colo800 WT or Colo800 TG tumour cells in co-culture conditions with cytotoxic MART-1-specific T-cells (n = 3/group) in the presence or absence of the lactate dehydrogenase inhibitor galloflavin. ( n ) Killing assay for Colo800 WT or Colo800 TG tumour cell growth in co-culture conditions with cytotoxic MART-1 T-cells (n = 4/group) in the presence or absence of the lactate efflux inhibitor AZD3965. ( o ) Glucose consumption of Colo800 WT and Colo800 TG cells cultured for 48 h (n = 6/group). ( p ) qRT-PCR analysis of indicated mRNAs from Colo800 WT and Colo800 TG cells (n = 6/group). Bold labelling depicts significant genes. ( q ) NMR metabolomics PLS − DA with coloured 95% confidence intervals illustrating the clear group separation in metabolic profile between Colo800 WT (n = 5) and Colo800 TG (n = 6) cells. ( r ) Top 15 metabolites and their VIP score based on the PLS − DA regression model. Scatter dot plot data are presented as mean values ± SEM. Line graph data are presented as mean values ± SEM (10a) or mean values ± SD (10j-k, m-n). Data in 10b-d,g,h,o,p were analysed by two-tailed unpaired t -test or Mann-Whitney test based on data normality distribution. Data in 10e were analysed by one-way ANOVA. Data in 10j,k were calculated for the area under the curve and analysed by two-tailed Student’s t -test. Data in 10m,n were calculated for the area under the curve and analysed by one-way ANOVA. In vitro co-culture schematics were created in BioRender. Heikenwälder, M. (2026) https://BioRender.com/lgjnsy9 .

Journal: Nature

Article Title: Activated ATF6α is a hepatic tumour driver restricting immunosurveillance

doi: 10.1038/s41586-025-10036-8

Figure Lengend Snippet: ( a-b ) Metabolic flux analysis ( a ) for extracellular acidification rates (ECAR) of FL83B WT (n = 3) or FL83B TG (n = 3) hepatocytes, with quantification ( b ) for glycolysis and glycolytic capacity. ( c ) Glucose consumption in FL83B WT or FL83B TG hepatocytes cultured for 48 h (n = 6/group). ( d ) qRT-PCR analysis of glucose-related metabolic genes in FL83B WT or FL83B TG cells (n = 6/group). Bold labelling depicts significant genes. ( e ) NMR spectroscopy-based metabolomics analysis of lactate concentration in FL83B cells with ATF6α expression (FL83B TG ) or deletion (FL83B KO ), normalized to respective controls (n = 6/group). ( f ) NMR metabolomics PLS − DA with coloured 95% confidence intervals illustrating the clear group separation in metabolic profile between FL83B WT and FL83B TG cells (n = 6/group). ( g ) qRT-PCR analysis of primary hepatocytes harvested from livers of 3-month-old TG Alb-cre− (n = 4) and TG Alb-cre+ (n = 6) mice. Bold labelling depicts significant genes. ( h ) qRT-PCR analysis of primary hepatocytes harvested from livers of CD-HFD-fed Atf6 fl/fl (n = 6) and Atf6 ΔHep (n = 6) mice. Bold labelling depicts significant genes. ( i ) Scheme of HCC cancer cell line (HLE) stably transfected with control vector (HLE WT ) or nATF6α-expressing (HLE TG ) plasmid and co-cultured with or without cytotoxic MART-1 T-cells to assess immune attack by a real-time cell analyzer (xCELLigence). ( j ) HLE WT or HLE TG cancer cell growth over time with quantification on the right panel (n = 3/group). ( k ) Killing assay and quantification for HLE WT or HLE TG cancer cell growth in co-culture conditions with cytotoxic MART-1 T-cells (n = 3/group). ( l ) Scheme of Colo800 tumour cells stably transfected with control (Colo800 WT ) or nATF6α-expressing (Colo800 TG ) plasmid and co-cultured with cytotoxic MART-1-specific T-cells to assess immune attack in a real-time cell analyzer (xCELLigence). ( m ) Killing assay of Colo800 WT or Colo800 TG tumour cells in co-culture conditions with cytotoxic MART-1-specific T-cells (n = 3/group) in the presence or absence of the lactate dehydrogenase inhibitor galloflavin. ( n ) Killing assay for Colo800 WT or Colo800 TG tumour cell growth in co-culture conditions with cytotoxic MART-1 T-cells (n = 4/group) in the presence or absence of the lactate efflux inhibitor AZD3965. ( o ) Glucose consumption of Colo800 WT and Colo800 TG cells cultured for 48 h (n = 6/group). ( p ) qRT-PCR analysis of indicated mRNAs from Colo800 WT and Colo800 TG cells (n = 6/group). Bold labelling depicts significant genes. ( q ) NMR metabolomics PLS − DA with coloured 95% confidence intervals illustrating the clear group separation in metabolic profile between Colo800 WT (n = 5) and Colo800 TG (n = 6) cells. ( r ) Top 15 metabolites and their VIP score based on the PLS − DA regression model. Scatter dot plot data are presented as mean values ± SEM. Line graph data are presented as mean values ± SEM (10a) or mean values ± SD (10j-k, m-n). Data in 10b-d,g,h,o,p were analysed by two-tailed unpaired t -test or Mann-Whitney test based on data normality distribution. Data in 10e were analysed by one-way ANOVA. Data in 10j,k were calculated for the area under the curve and analysed by two-tailed Student’s t -test. Data in 10m,n were calculated for the area under the curve and analysed by one-way ANOVA. In vitro co-culture schematics were created in BioRender. Heikenwälder, M. (2026) https://BioRender.com/lgjnsy9 .

Article Snippet: Clear supernatant was filled into 1.7 mm Bruker SampleJet-compatible NMR spectroscopy tubes.

Techniques: Cell Culture, Quantitative RT-PCR, Structural Proteomics, Concentration Assay, Expressing, Stable Transfection, Transfection, Control, Plasmid Preparation, Co-Culture Assay, Two Tailed Test, MANN-WHITNEY, In Vitro