glass slide arraying system Search Results


glass-backed nitrocellulose array slide  (SCHOTT)
90
SCHOTT glass-backed nitrocellulose array slide
Glass Backed Nitrocellulose Array Slide, supplied by SCHOTT, 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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rat antibody array 90 glass slide kit  (RayBiotech inc)
90
RayBiotech inc rat antibody array 90 glass slide kit
Rat Antibody Array 90 Glass Slide Kit, supplied by RayBiotech 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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rat antibody array 90 glass slide kit - by Bioz Stars, 2026-05
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glass slides with tissue array of various liver diseases  (Biomax Inc)
90
Biomax Inc glass slides with tissue array of various liver diseases
Glass Slides With Tissue Array Of Various Liver Diseases, supplied by Biomax 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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p. aeruginosa pao1 glass slide arrays  (Arbor Biosciences)
90
Arbor Biosciences p. aeruginosa pao1 glass slide arrays
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
P. Aeruginosa Pao1 Glass Slide Arrays, supplied by Arbor Biosciences, 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/p. aeruginosa pao1 glass slide arrays/product/Arbor Biosciences
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p. aeruginosa pao1 glass slide arrays - by Bioz Stars, 2026-05
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array of antibodies printed on glass slides  (Full Moon BioSystems)
90
Full Moon BioSystems array of antibodies printed on glass slides
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Array Of Antibodies Printed On Glass Slides, supplied by Full Moon BioSystems, 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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array of antibodies printed on glass slides - by Bioz Stars, 2026-05
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glass slide-based peptide array  (JPT Peptide Technologies GmbH)
90
JPT Peptide Technologies GmbH glass slide-based peptide array
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Glass Slide Based Peptide Array, supplied by JPT Peptide Technologies 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/glass slide-based peptide array/product/JPT Peptide Technologies GmbH
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glass slide-based peptide array - by Bioz Stars, 2026-05
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mouse inflammation array 1 glass slide  (RayBiotech inc)
90
RayBiotech inc mouse inflammation array 1 glass slide
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Mouse Inflammation Array 1 Glass Slide, supplied by RayBiotech 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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mouse inflammation array 1 glass slide - by Bioz Stars, 2026-05
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mouse l1308 array glass slide kit  (RayBiotech inc)
90
RayBiotech inc mouse l1308 array glass slide kit
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Mouse L1308 Array Glass Slide Kit, supplied by RayBiotech 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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raybio ® human 55 biotin-label based obesity antibody arrays (human l-182 array, glass slide,  (RayBiotech inc)
90
RayBiotech inc raybio ® human 55 biotin-label based obesity antibody arrays (human l-182 array, glass slide,
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Raybio ® Human 55 Biotin Label Based Obesity Antibody Arrays (Human L 182 Array, Glass Slide,, supplied by RayBiotech inc, 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/raybio ® human 55 biotin-label based obesity antibody arrays (human l-182 array, glass slide,/product/RayBiotech inc
Average 90 stars, based on 1 article reviews
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array glass slide  (Kaneka Corp)
90
Kaneka Corp array glass slide
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Array Glass Slide, supplied by Kaneka Corp, 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/array glass slide/product/Kaneka Corp
Average 90 stars, based on 1 article reviews
array glass slide - by Bioz Stars, 2026-05
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celluspot glass slide histone tail peptide array  (INTAVIS Inc)
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INTAVIS Inc celluspot glass slide histone tail peptide array
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Celluspot Glass Slide Histone Tail Peptide Array, supplied by INTAVIS 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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glass-slide-mounted expressed sequence tag (est) arrays of soybean  (Unigene)
90
Unigene glass-slide-mounted expressed sequence tag (est) arrays of soybean
Induction of planktonic mode of growth in P. <t>aeruginosa</t> <t>PAO1</t> biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.
Glass Slide Mounted Expressed Sequence Tag (Est) Arrays Of Soybean, supplied by Unigene, 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


Induction of planktonic mode of growth in P. aeruginosa PAO1 biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.

Journal: Frontiers in Microbiology

Article Title: Dissection of the cis -2-decenoic acid signaling network in Pseudomonas aeruginosa using microarray technique

doi: 10.3389/fmicb.2015.00383

Figure Lengend Snippet: Induction of planktonic mode of growth in P. aeruginosa PAO1 biofilms by CDA. (A) Determination of cell density using semi-batch cultures. P. aeruginosa biofilms were grown for 5 days in petri dishes. Dispersion by CDA was tested at concentrations between 100 and 620 nM (carrier used as a control). Cell density was determined by measuring the optical density. (B) Determination of cell density using continuous cultures. Biofilms of P. aeruginosa PAO1 were grown in flow cell continuous cultures, and dispersed by given CDA concentrations or the carrier. Effluent runoffs were then collected and cell density was determined. (C) Quantification of percent surface coverage. P. aeruginosa PAO1 biofilms remaining on the surface were then stained with 3 μl/ml SYTO 9 to allow analysis using fluorescence microscopy and percent surface coverage was quantified using digital image analysis. Error bars indicate SD ( n = 3). (D) Stained biofilms before and after treatments by CDA. Images are top-down views (x-y plane); scale bars: 50 μm.

Article Snippet: P. aeruginosa PAO1 glass slide arrays (Mycroarray Inc.) were scanned using a ScanArray Express scanner (Perkin-Elmer).

Techniques: Dispersion, Control, Staining, Fluorescence, Microscopy

Functional classifications of DE genes in P. aeruginosa after treatment with 100 nM CDA. (A) DE genes were classified in to more than 15 functional groups. The top functional classes with the percentages of genes altered in each class were presented in the pie graph. (B) Percentages of up and down regulated genes in each functional group.

Journal: Frontiers in Microbiology

Article Title: Dissection of the cis -2-decenoic acid signaling network in Pseudomonas aeruginosa using microarray technique

doi: 10.3389/fmicb.2015.00383

Figure Lengend Snippet: Functional classifications of DE genes in P. aeruginosa after treatment with 100 nM CDA. (A) DE genes were classified in to more than 15 functional groups. The top functional classes with the percentages of genes altered in each class were presented in the pie graph. (B) Percentages of up and down regulated genes in each functional group.

Article Snippet: P. aeruginosa PAO1 glass slide arrays (Mycroarray Inc.) were scanned using a ScanArray Express scanner (Perkin-Elmer).

Techniques: Functional Assay

Comparison of microarray and semi-qRT PCR analyses of 5 selected genes in P. aeruginosa biofilm cells exposed to 100 nM CDA and in untreated biofilm cells . Error bars indicate SD ( n = 3).

Journal: Frontiers in Microbiology

Article Title: Dissection of the cis -2-decenoic acid signaling network in Pseudomonas aeruginosa using microarray technique

doi: 10.3389/fmicb.2015.00383

Figure Lengend Snippet: Comparison of microarray and semi-qRT PCR analyses of 5 selected genes in P. aeruginosa biofilm cells exposed to 100 nM CDA and in untreated biofilm cells . Error bars indicate SD ( n = 3).

Article Snippet: P. aeruginosa PAO1 glass slide arrays (Mycroarray Inc.) were scanned using a ScanArray Express scanner (Perkin-Elmer).

Techniques: Comparison, Microarray, Quantitative RT-PCR

Removal of established biofilms of P. aeruginosa , using CDA combined by antimicrobial treatments . Following dispersion of biofilms by CDA, cells remaining on the surface were easily killed and removed by various antimicrobial compounds (tobramycin; Tob, H 2 O 2 , ciprofloxacin; Cip). (A) LIVE/DEAD staining of biofilms. 48 h-old-biofilms of P. aeruginosa were treated with indicated antimicrobials alone or combined with 100 nM CDA for only 1 h. Biofilms were then stained with LIVE/DEAD staining and (B) Quantification of percent surface coverage. After LIVE/DEAD staining percent surface coverage was quantified using digital image analysis. Images are top-down views (x-y plane); scale bars: 50 μm. Error bars indicate SD ( n = 3).

Journal: Frontiers in Microbiology

Article Title: Dissection of the cis -2-decenoic acid signaling network in Pseudomonas aeruginosa using microarray technique

doi: 10.3389/fmicb.2015.00383

Figure Lengend Snippet: Removal of established biofilms of P. aeruginosa , using CDA combined by antimicrobial treatments . Following dispersion of biofilms by CDA, cells remaining on the surface were easily killed and removed by various antimicrobial compounds (tobramycin; Tob, H 2 O 2 , ciprofloxacin; Cip). (A) LIVE/DEAD staining of biofilms. 48 h-old-biofilms of P. aeruginosa were treated with indicated antimicrobials alone or combined with 100 nM CDA for only 1 h. Biofilms were then stained with LIVE/DEAD staining and (B) Quantification of percent surface coverage. After LIVE/DEAD staining percent surface coverage was quantified using digital image analysis. Images are top-down views (x-y plane); scale bars: 50 μm. Error bars indicate SD ( n = 3).

Article Snippet: P. aeruginosa PAO1 glass slide arrays (Mycroarray Inc.) were scanned using a ScanArray Express scanner (Perkin-Elmer).

Techniques: Dispersion, Staining

Comparison of predicted and known proteins involved in CDA and DSF synthesis and perception. (A) CDA synthesis and perception in P. aeruginosa based on known PPIs. (B) Demonstrated DSF synthesis and perception in Xcc .

Journal: Frontiers in Microbiology

Article Title: Dissection of the cis -2-decenoic acid signaling network in Pseudomonas aeruginosa using microarray technique

doi: 10.3389/fmicb.2015.00383

Figure Lengend Snippet: Comparison of predicted and known proteins involved in CDA and DSF synthesis and perception. (A) CDA synthesis and perception in P. aeruginosa based on known PPIs. (B) Demonstrated DSF synthesis and perception in Xcc .

Article Snippet: P. aeruginosa PAO1 glass slide arrays (Mycroarray Inc.) were scanned using a ScanArray Express scanner (Perkin-Elmer).

Techniques: Comparison