Structured Review

FUJIFILM chemiluminescence
Chemiluminescence, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 92/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/chemiluminescence/product/FUJIFILM
Average 92 stars, based on 8 article reviews
Price from $9.99 to $1999.99
chemiluminescence - by Bioz Stars, 2020-07
92/100 stars

Images

Related Articles

other:

Article Title: Type II restriction modification system in Ureaplasma parvum OMC-P162 strain
Article Snippet: Following treatment with horseradish peroxidase-conjugated secondary antibody (Rockland Immunochemicals, PA, USA), the tagged proteins were visualized via chemiluminescence (LAS-4000; Fujifilm, Tokyo, Japan).

Article Title: Decay-Accelerating Factor Mitigates Controlled Hemorrhage-Instigated Intestinal and Lung Tissue Damage and Hyperkalemia in Swine
Article Snippet: Specific bands were visualized by the Enhanced Chemiluminescence (ECL) method (Amersham Biosciences, Piscataway, NJ) and captured with Fujifilm LAS-3000 System Configured for Chemiluminescence (Fujifilm Life Science, Edison, NJ).

Article Title: Vasoactive intestinal peptide increases apoptosis of hepatocellular carcinoma by inhibiting the cAMP/Bcl‐ xL pathway, et al. Vasoactive intestinal peptide increases apoptosis of hepatocellular carcinoma by inhibiting the cAMP/Bcl‐xL pathway
Article Snippet: Reactive proteins were detected by means of enhanced chemiluminescence (ImmnoStar, Wako, Tokyo).

Article Title: Decay-Accelerating Factor Mitigates Controlled Hemorrhage-Instigated Intestinal and Lung Tissue Damage and Hyperkalemia in Swine
Article Snippet: Specific bands were visualized by the ECL method (Amersham Biosciences, Piscataway, NJ) and captured with Fujifilm LAS-3000 System Configured for Chemiluminescence (Fujifilm Life Science, Edison, NJ).

Article Title: Differential regulation of muscle protein turnover in response to emphysema and acute pulmonary inflammation
Article Snippet: Blots were then washed and probed with a horseradish peroxidase-conjugated secondary antibody (Vector Laboratories, Burlingame, CA) and visualized with chemiluminescence (Supersignal West Pico or Femto Chemiluminescent Substrate; Pierce Biotechnology) in a LAS-3000 Luminescent Image analyzer (Fujifilm, Tokyo, Japan).

Article Title: Vitamin D Attenuates Endothelial Dysfunction in Uremic Rats and Maintains Human Endothelial Stability
Article Snippet: Signal was visualized using enhanced chemiluminescence (Life Sciences) on LAS3000 (Fujifilm, Japan).

Article Title: Chronic high dose of captopril induces depressive-like behaviors in mice: possible mechanism of regulatory T cell in depression
Article Snippet: Then, the membranes were then exposed to chemiluminescence (LAS- 4000, Fujifilm) for detection of light emission.

Software:

Article Title: (-) Epigallocatechin gallate suppresses the differentiation of 3T3-L1 preadipocytes through transcription factors FoxO1 and SREBP1c
Article Snippet: .. Finally, each protein band was detected by chemiluminescence (Las 1000, Fuji FILM, Minato, Tokyo, Japan), and analyzed with Image Gauge Software (FUJI-FILM). .. Anti-FoxO1 (Cell signaling), anti-phospho-FoxO1 (Thr24) (Cell signaling), anti-phospho-FoxO1 (Ser256) (Cell signaling) and anti-β-actin (Sigma) were used as primary antibodies.

Similar Products

  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 85
    FUJIFILM photostimulated luminescence intensities
    Distribution patterns of 32 P, 35 S, and 45 Ca in each organ 15min and 48h after the initiation of treatment. (A–F) 32 P (A, B), 35 S (C, D), and 45 Ca (E, F) signals were analysed with an imaging plate (IP) at 15min (A, C, E) and 48h (B, D, F) after the initiation of treatment. The signal intensity for each organ was based on the <t>photostimulated</t> luminescence value, which was normalized to the value for the L3 sheath of each plant, and was quantified considering the amount of each radionuclide in the L3 sheath at 15min as a standard. Error bars correspond to standard deviation from three biological repeats. (G, H) Distribution pattern of 45 Ca in each organ at 15min (G) and 48h (H) are shown in representative IP images. The leaf samples in (G) are shown in order from L2 (far left) to L7 (far right). L3, L4, L5, and L6 were separated into the corresponding sheath and blade (left and right, respectively, in each pair of organs). The photograph of the analysed plant tissues (G, left) shows the positions of the samples in the detected 45 Ca image (G, right). Arrows are appended to assist the recognition of 45 Ca signals. The leaf samples in (H) were positioned as in (G), except that an L8 image could be detected and is shown at the far right. Experiments were performed at least twice, providing similar results (this figure is available in colour at JXB online).
    Photostimulated Luminescence Intensities, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 85/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/photostimulated luminescence intensities/product/FUJIFILM
    Average 85 stars, based on 11 article reviews
    Price from $9.99 to $1999.99
    photostimulated luminescence intensities - by Bioz Stars, 2020-07
    85/100 stars
      Buy from Supplier

    85
    FUJIFILM las 1000 luminescence detector
    Cytokine array analysis of rat intestinal loops washes. Layout of the arrays (A), cytokine profiles from loops treated with PBS (control) (B), gliadin (C), gliadin+IFN-γ (D), B. bifidum IATA-ES2+gliadin+IFN-γ (E), E. coli CBL2+gliadin+IFN-γ (F), and E. coli CBL2+ B. bifidum IATA-ES2+gliadin+IFN-γ (G). The data are expressed as relative levels of selected cytokines (percentage of positive controls). Cytokine-induced neutrophil chemoattractant (CINC)-2 and -3, monocyte chemoattractant protein (MCP)-1, macrophage inflammatory protein (MIP)-3α, nerve growth factor β-(NGF), tumor necrosis factor (TNF)-α, vascular endothelial growth factor (VEGF). The signal intensity was measured using the <t>LAS-1000</t> luminescence detector (Fujifilm, Tokyo, Japan).
    Las 1000 Luminescence Detector, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 85/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/las 1000 luminescence detector/product/FUJIFILM
    Average 85 stars, based on 5 article reviews
    Price from $9.99 to $1999.99
    las 1000 luminescence detector - by Bioz Stars, 2020-07
    85/100 stars
      Buy from Supplier

    Image Search Results


    Distribution patterns of 32 P, 35 S, and 45 Ca in each organ 15min and 48h after the initiation of treatment. (A–F) 32 P (A, B), 35 S (C, D), and 45 Ca (E, F) signals were analysed with an imaging plate (IP) at 15min (A, C, E) and 48h (B, D, F) after the initiation of treatment. The signal intensity for each organ was based on the photostimulated luminescence value, which was normalized to the value for the L3 sheath of each plant, and was quantified considering the amount of each radionuclide in the L3 sheath at 15min as a standard. Error bars correspond to standard deviation from three biological repeats. (G, H) Distribution pattern of 45 Ca in each organ at 15min (G) and 48h (H) are shown in representative IP images. The leaf samples in (G) are shown in order from L2 (far left) to L7 (far right). L3, L4, L5, and L6 were separated into the corresponding sheath and blade (left and right, respectively, in each pair of organs). The photograph of the analysed plant tissues (G, left) shows the positions of the samples in the detected 45 Ca image (G, right). Arrows are appended to assist the recognition of 45 Ca signals. The leaf samples in (H) were positioned as in (G), except that an L8 image could be detected and is shown at the far right. Experiments were performed at least twice, providing similar results (this figure is available in colour at JXB online).

    Journal: Journal of Experimental Botany

    Article Title: Characterization of rapid intervascular transport of cadmium in rice stem by radioisotope imaging

    doi: 10.1093/jxb/ers344

    Figure Lengend Snippet: Distribution patterns of 32 P, 35 S, and 45 Ca in each organ 15min and 48h after the initiation of treatment. (A–F) 32 P (A, B), 35 S (C, D), and 45 Ca (E, F) signals were analysed with an imaging plate (IP) at 15min (A, C, E) and 48h (B, D, F) after the initiation of treatment. The signal intensity for each organ was based on the photostimulated luminescence value, which was normalized to the value for the L3 sheath of each plant, and was quantified considering the amount of each radionuclide in the L3 sheath at 15min as a standard. Error bars correspond to standard deviation from three biological repeats. (G, H) Distribution pattern of 45 Ca in each organ at 15min (G) and 48h (H) are shown in representative IP images. The leaf samples in (G) are shown in order from L2 (far left) to L7 (far right). L3, L4, L5, and L6 were separated into the corresponding sheath and blade (left and right, respectively, in each pair of organs). The photograph of the analysed plant tissues (G, left) shows the positions of the samples in the detected 45 Ca image (G, right). Arrows are appended to assist the recognition of 45 Ca signals. The leaf samples in (H) were positioned as in (G), except that an L8 image could be detected and is shown at the far right. Experiments were performed at least twice, providing similar results (this figure is available in colour at JXB online).

    Article Snippet: The net photostimulated luminescence intensities in each leaf part were calculated using image analysis software (Image Gauge version 4.0, Fujifilm).

    Techniques: Imaging, Standard Deviation

    Time-dependent changes in the distribution pattern of 109 Cd in each organ. (A) The amount of 109 Cd in the leaves at 15min was measured using a gamma counter and normalized to that of L5. (B–D) 109 Cd signals in the sheath and blade of each leaf were analysed at 1 (B), 3 (C), and 48h (D) after the initiation of treatment. Signal intensities, based on the photostimulated luminescence values for each organ, were normalized to those of the L3 sheath within each plant. Amount of 109 Cd relative to that in the L3 sheath at 1h was presented. Error bars correspond to standard deviation from three biological repeats. Experiments were performed at least twice, providing similar results. (E) Typical distribution pattern of 109 Cd detected by an imaging plate at 1h (bottom panel) is shown together with a photograph of the organs analysed (top panel). Samples were positioned in order from L2 (far left) to L7 (far right). L3, L4, L5, and L6 were separated into sheaths (left) and blades (right). Arrows are appended to assist the recognition of 109 Cd signals in L7. (F) Images of the distribution pattern of 109 Cd in L4 at 1, 3, and 48h after the initiation of treatment. For each time point in (F), the photograph on the left corresponds to the image on the right. Within each panel, the organs are arranged with the sheaths on the left and the blades on the right. Experiments were performed at least twice, providing similar results (this figure is available in colour at JXB online).

    Journal: Journal of Experimental Botany

    Article Title: Characterization of rapid intervascular transport of cadmium in rice stem by radioisotope imaging

    doi: 10.1093/jxb/ers344

    Figure Lengend Snippet: Time-dependent changes in the distribution pattern of 109 Cd in each organ. (A) The amount of 109 Cd in the leaves at 15min was measured using a gamma counter and normalized to that of L5. (B–D) 109 Cd signals in the sheath and blade of each leaf were analysed at 1 (B), 3 (C), and 48h (D) after the initiation of treatment. Signal intensities, based on the photostimulated luminescence values for each organ, were normalized to those of the L3 sheath within each plant. Amount of 109 Cd relative to that in the L3 sheath at 1h was presented. Error bars correspond to standard deviation from three biological repeats. Experiments were performed at least twice, providing similar results. (E) Typical distribution pattern of 109 Cd detected by an imaging plate at 1h (bottom panel) is shown together with a photograph of the organs analysed (top panel). Samples were positioned in order from L2 (far left) to L7 (far right). L3, L4, L5, and L6 were separated into sheaths (left) and blades (right). Arrows are appended to assist the recognition of 109 Cd signals in L7. (F) Images of the distribution pattern of 109 Cd in L4 at 1, 3, and 48h after the initiation of treatment. For each time point in (F), the photograph on the left corresponds to the image on the right. Within each panel, the organs are arranged with the sheaths on the left and the blades on the right. Experiments were performed at least twice, providing similar results (this figure is available in colour at JXB online).

    Article Snippet: The net photostimulated luminescence intensities in each leaf part were calculated using image analysis software (Image Gauge version 4.0, Fujifilm).

    Techniques: Standard Deviation, Imaging

    Inhibition of tRNA transcription in vitro by UK-118005. (A) In vitro transcription of SUP53 (left panel) and SUP4 (right panel) in the presence or absence of UK-118005 for 1 h; (B) quantitation of dose-dependent inhibition of SUP4 in vitro transcription by UK-118005. Quantitation of radiolabeled tRNA is expressed in photostimulated luminescence (PSL) units. (Top panel) transcription with wild-type RNA Pol III nuclear extract; (bottom panel) transcription with RPO31-G1101S mutant RNA Pol III nuclear extract.

    Journal: Eukaryotic Cell

    Article Title: Novel Small-Molecule Inhibitors of RNA Polymerase III

    doi: 10.1128/EC.2.2.256-264.2003

    Figure Lengend Snippet: Inhibition of tRNA transcription in vitro by UK-118005. (A) In vitro transcription of SUP53 (left panel) and SUP4 (right panel) in the presence or absence of UK-118005 for 1 h; (B) quantitation of dose-dependent inhibition of SUP4 in vitro transcription by UK-118005. Quantitation of radiolabeled tRNA is expressed in photostimulated luminescence (PSL) units. (Top panel) transcription with wild-type RNA Pol III nuclear extract; (bottom panel) transcription with RPO31-G1101S mutant RNA Pol III nuclear extract.

    Article Snippet: The activity of the RNA Pol III in vitro transcription was quantitated by measuring the photostimulated luminescence units from radiolabeled tRNA products on a Fujifilm BAS-2500 phosphorimager.

    Techniques: Inhibition, In Vitro, Quantitation Assay, Mutagenesis

    (A) Comparison of the quantitative regional distribution of 89 Zr-df–L2mAb in U87-MG, NCI-H460, T-47D, MKN-45, A-431,and DLD-1 tumor whole sections and specific ROIs of high and low density areas from in vitro autoradiography studies. Each bar represents the mean specific bound 89 Zr-df–L2mAb ± SD ( B sp ; B t – B nsb ) in photostimulated luminescence units per mm 2 (PSL/mm 2 ) calculated from ROIs representing total 89 Zr-L2mAb bound ( B t ) and corresponding ROIs representing nonspecific binding (+ 10 –6 M L2mAb) [high density ROIs, n = 4; whole section ROIs, n = 2; low density ROIs, n = 4]. The bars representing quantitative vessel counts (vessel counts/10 –7 μm 2 ) are the mean ± SD ( n = 2) determined from CD31 IHC staining of whole sections. (B) Correlation of whole section ROIs (PSL/mm 2 , 89 Zr-df–L2mAb specific binding) to vessel density (vessels per 10 –7 μm 2 ), Spearman r = 0.7622, P = 0.0055. (C) Comparison of TEM8 protein in A431, DLD-1, MKN-45, NCI-H460, T-47D, and U87-MG cells and tumors determined by immunoprecipitation and Western blotting.

    Journal: Molecular Pharmaceutics

    Article Title: Immuno-PET Imaging of Tumor Endothelial Marker 8 (TEM8)

    doi: 10.1021/mp500056d

    Figure Lengend Snippet: (A) Comparison of the quantitative regional distribution of 89 Zr-df–L2mAb in U87-MG, NCI-H460, T-47D, MKN-45, A-431,and DLD-1 tumor whole sections and specific ROIs of high and low density areas from in vitro autoradiography studies. Each bar represents the mean specific bound 89 Zr-df–L2mAb ± SD ( B sp ; B t – B nsb ) in photostimulated luminescence units per mm 2 (PSL/mm 2 ) calculated from ROIs representing total 89 Zr-L2mAb bound ( B t ) and corresponding ROIs representing nonspecific binding (+ 10 –6 M L2mAb) [high density ROIs, n = 4; whole section ROIs, n = 2; low density ROIs, n = 4]. The bars representing quantitative vessel counts (vessel counts/10 –7 μm 2 ) are the mean ± SD ( n = 2) determined from CD31 IHC staining of whole sections. (B) Correlation of whole section ROIs (PSL/mm 2 , 89 Zr-df–L2mAb specific binding) to vessel density (vessels per 10 –7 μm 2 ), Spearman r = 0.7622, P = 0.0055. (C) Comparison of TEM8 protein in A431, DLD-1, MKN-45, NCI-H460, T-47D, and U87-MG cells and tumors determined by immunoprecipitation and Western blotting.

    Article Snippet: Regions of interest (ROIs) from the digitized images, expressed as photostimulated luminescence units per mm2 (PSL/mm2 ), were drawn for the whole tumor slice, and the high and low density areas within the section, using Image Gauge 4.0 (Fujifilm, Tokyo, Japan) which represented 89 Zr-df–L2mAb “total” binding (B t ).

    Techniques: In Vitro, Autoradiography, Binding Assay, Immunohistochemistry, Staining, Immunoprecipitation, Western Blot

    Cytokine array analysis of rat intestinal loops washes. Layout of the arrays (A), cytokine profiles from loops treated with PBS (control) (B), gliadin (C), gliadin+IFN-γ (D), B. bifidum IATA-ES2+gliadin+IFN-γ (E), E. coli CBL2+gliadin+IFN-γ (F), and E. coli CBL2+ B. bifidum IATA-ES2+gliadin+IFN-γ (G). The data are expressed as relative levels of selected cytokines (percentage of positive controls). Cytokine-induced neutrophil chemoattractant (CINC)-2 and -3, monocyte chemoattractant protein (MCP)-1, macrophage inflammatory protein (MIP)-3α, nerve growth factor β-(NGF), tumor necrosis factor (TNF)-α, vascular endothelial growth factor (VEGF). The signal intensity was measured using the LAS-1000 luminescence detector (Fujifilm, Tokyo, Japan).

    Journal: PLoS ONE

    Article Title: Role of Intestinal Bacteria in Gliadin-Induced Changes in Intestinal Mucosa: Study in Germ-Free Rats

    doi: 10.1371/journal.pone.0016169

    Figure Lengend Snippet: Cytokine array analysis of rat intestinal loops washes. Layout of the arrays (A), cytokine profiles from loops treated with PBS (control) (B), gliadin (C), gliadin+IFN-γ (D), B. bifidum IATA-ES2+gliadin+IFN-γ (E), E. coli CBL2+gliadin+IFN-γ (F), and E. coli CBL2+ B. bifidum IATA-ES2+gliadin+IFN-γ (G). The data are expressed as relative levels of selected cytokines (percentage of positive controls). Cytokine-induced neutrophil chemoattractant (CINC)-2 and -3, monocyte chemoattractant protein (MCP)-1, macrophage inflammatory protein (MIP)-3α, nerve growth factor β-(NGF), tumor necrosis factor (TNF)-α, vascular endothelial growth factor (VEGF). The signal intensity was measured using the LAS-1000 luminescence detector (Fujifilm, Tokyo, Japan).

    Article Snippet: The signal intensity was measured on an LAS-1000 luminescence detector (Fujifilm), and the resulting images were analyzed using AIDA software (version 3.28; Raytest) to quantify spot densities.

    Techniques: