stainless steel needle 12.5μm diameter Search Results


90
Renfert GmbH 125μm al 2 o 3 cobra
125μm Al 2 O 3 Cobra, supplied by Renfert GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/125μm al 2 o 3 cobra/product/Renfert GmbH
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125μm al 2 o 3 cobra - by Bioz Stars, 2026-02
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Trinity Brand Industries 316l stainless steel
316l Stainless Steel, supplied by Trinity Brand Industries, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/316l stainless steel/product/Trinity Brand Industries
Average 90 stars, based on 1 article reviews
316l stainless steel - by Bioz Stars, 2026-02
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Millipore 3 h palmitic acid
3 H Palmitic Acid, supplied by Millipore, 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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Cospheric LLC fluorescent green pe microspheres
Fluorescent Green Pe Microspheres, supplied by Cospheric LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fluorescent green pe microspheres/product/Cospheric LLC
Average 90 stars, based on 1 article reviews
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A-M Systems ag/agcl wire
Ag/Agcl Wire, supplied by A-M Systems, 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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Thermo Fisher 12.5μm sytox orange nucleic acid stain
A-C: Images of <t>SYTOX</t> Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA <t>from</t> <t>PMNs</t> incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).
12.5μm Sytox Orange Nucleic Acid Stain, 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
https://www.bioz.com/result/12.5μm sytox orange nucleic acid stain/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
12.5μm sytox orange nucleic acid stain - by Bioz Stars, 2026-02
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Cedarlane cisplatin
A-C: Images of <t>SYTOX</t> Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA <t>from</t> <t>PMNs</t> incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).
Cisplatin, supplied by Cedarlane, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cisplatin/product/Cedarlane
Average 90 stars, based on 1 article reviews
cisplatin - by Bioz Stars, 2026-02
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Thorlabs tapered multimode optical fiber (105/125μm core/cladding diameters) afs105/125y
A-C: Images of <t>SYTOX</t> Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA <t>from</t> <t>PMNs</t> incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).
Tapered Multimode Optical Fiber (105/125μm Core/Cladding Diameters) Afs105/125y, supplied by Thorlabs, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tapered multimode optical fiber (105/125μm core/cladding diameters) afs105/125y/product/Thorlabs
Average 90 stars, based on 1 article reviews
tapered multimode optical fiber (105/125μm core/cladding diameters) afs105/125y - by Bioz Stars, 2026-02
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Carl Zeiss rasterelektronenmikroskop evo50
A-C: Images of <t>SYTOX</t> Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA <t>from</t> <t>PMNs</t> incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).
Rasterelektronenmikroskop Evo50, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rasterelektronenmikroskop evo50/product/Carl Zeiss
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Millipore pervanadate
A-C: Images of <t>SYTOX</t> Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA <t>from</t> <t>PMNs</t> incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).
Pervanadate, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/pervanadate/product/Millipore
Average 90 stars, based on 1 article reviews
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BGB Analytik spe bulk sorbent carbograph s*pure extract-clean spe bulk packing material, 38-125μm
A-C: Images of <t>SYTOX</t> Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA <t>from</t> <t>PMNs</t> incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).
Spe Bulk Sorbent Carbograph S*Pure Extract Clean Spe Bulk Packing Material, 38 125μm, supplied by BGB Analytik, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/spe bulk sorbent carbograph s*pure extract-clean spe bulk packing material, 38-125μm/product/BGB Analytik
Average 90 stars, based on 1 article reviews
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Cospheric LLC fluorescent bead fluorescent green pe microspheres uvms-bg-1.00
Representative frames from example videos ( & ) a) Raw (unprocessed) fluorescence signal (cyan wavelength). A <t>fluorescent</t> bead placed within the dental cement at the right anterior edge of the surgical preparation is indicated (white arrow). The bead is used for right and left identification and motion correction. b) Data from a) after processing. c) Estimated motion parameters based on position of fluorescent bead.
Fluorescent Bead Fluorescent Green Pe Microspheres Uvms Bg 1.00, supplied by Cospheric LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fluorescent bead fluorescent green pe microspheres uvms-bg-1.00/product/Cospheric LLC
Average 90 stars, based on 1 article reviews
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Image Search Results


A-C: Images of SYTOX Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA from PMNs incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).

Journal: PLoS Neglected Tropical Diseases

Article Title: Human Leukocytes Kill Brugia malayi Microfilariae Independently of DNA-Based Extracellular Trap Release

doi: 10.1371/journal.pntd.0005279

Figure Lengend Snippet: A-C: Images of SYTOX Orange-labelled extracellular DNA present within Mf-treated (A), zero Mf (negative control) (B) and PMA-treated (positive control) (C) wells. The images were taken 7 hours post-assay set up. These wells did not contain serum. D-G: Changes in mean SYTOX Orange intensity were used to monitor the release of extracellular DNA from PMNs incubated for 7 hours in vitro . In each panel, the dotted lines indicate the Standard Error of the mean fluorescence intensity. D: 25nM phorbol myristate acetate (PMA)- and Mf-induced DNA release in the absence of serum was measured as described in Materials and Methods (n = 7). E: 10μM diphenyleneiodonium (DPI) and 30μg/ml DNAse I inhibited Mf-induced DNA release in the absence of serum (n≥4). F: Extracellular DNA release in Mf- and PMA-treated wells that contained 5% autologous serum (n = 6). G: 5% autologous serum and 5% autologous heat treated serum (HTS) inhibited Mf induced DNA release (n≥6).

Article Snippet: PMNs were suspended in RPMI-1640 containing 12.5μM SYTOX Orange Nucleic Acid Stain (Life Technologies, Eugene, OR, USA) to give a final concentration of 3.125μM of SYTOX Orange stain and enable the quantification of extracellular DNA [ , ].

Techniques: Negative Control, Positive Control, Incubation, In Vitro, Fluorescence

Representative frames from example videos ( & ) a) Raw (unprocessed) fluorescence signal (cyan wavelength). A fluorescent bead placed within the dental cement at the right anterior edge of the surgical preparation is indicated (white arrow). The bead is used for right and left identification and motion correction. b) Data from a) after processing. c) Estimated motion parameters based on position of fluorescent bead.

Journal: Nature methods

Article Title: Simultaneous cortex-wide fluorescence Ca 2+ imaging and whole-brain fMRI

doi: 10.1038/s41592-020-00984-6

Figure Lengend Snippet: Representative frames from example videos ( & ) a) Raw (unprocessed) fluorescence signal (cyan wavelength). A fluorescent bead placed within the dental cement at the right anterior edge of the surgical preparation is indicated (white arrow). The bead is used for right and left identification and motion correction. b) Data from a) after processing. c) Estimated motion parameters based on position of fluorescent bead.

Article Snippet: A fluorescent bead (Fluorescent green PE microspheres, UVMS-BG-1.00, 106–125μm, Cospheric) is embedded within the right-anterior wall for motion correction.

Techniques: Fluorescence