fluoro-gel ii mounting media containing dapi Search Results


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Shanghai Macklin Biochemical fluorescent dyes dapi
Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with <t>DAPI.</t>
Fluorescent Dyes Dapi, supplied by Shanghai Macklin Biochemical, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bachem fluorogenic substrate mca-pro-leu-ala-gln-ala-val-dap (dpn)-arg-serser-ser-ser-arg-nh2
Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with <t>DAPI.</t>
Fluorogenic Substrate Mca Pro Leu Ala Gln Ala Val Dap (Dpn) Arg Serser Ser Ser Arg Nh2, supplied by Bachem, 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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AnaSpec fluorogenic mmp substrate xi (5-fam-procha-gly-nva-his-ala-dap(qxltm520)-nh2
Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with <t>DAPI.</t>
Fluorogenic Mmp Substrate Xi (5 Fam Procha Gly Nva His Ala Dap(qxltm520) Nh2, supplied by AnaSpec, 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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Nikon eclipse e800 upright fluorescence microscope
Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with <t>DAPI.</t>
Eclipse E800 Upright Fluorescence Microscope, supplied by Nikon, 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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AnaSpec mmp fluorogenic substrate xi 5-fam-p-cha-g-nva-ha-dap(qxltm 520)-nh2
Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with <t>DAPI.</t>
Mmp Fluorogenic Substrate Xi 5 Fam P Cha G Nva Ha Dap(qxltm 520) Nh2, supplied by AnaSpec, 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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Interchim Chemicals fluoro gel mounting medium with dapi
Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with <t>DAPI.</t>
Fluoro Gel Mounting Medium With Dapi, supplied by Interchim Chemicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carl Zeiss lsm 780 confocal microscope
Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with <t>DAPI.</t>
Lsm 780 Confocal Microscope, 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
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Biozol Diagnostica Vertrieb GmbH quenched fluorogenic peptide substrate abz–leu–ala–gln–ala–val–arg–ser–ser–ser–arg–dap(dnp)–nh2
ADAM17 is proteolytically active on isolated ascites‐EV. ADAM17 proteolytic activity of ascites‐EV was quantified using a cell‐free ADAM17 activity assay. 1 × 10 9 ascites‐EV of three OvCa patients (#1, #2 and #3) or PBS as a control were incubated at 37°C for 80 min with a <t>fluorogenic</t> substrate. Relative fluorescence units (RFU) were measured every 30 s. RFU of the PBS control was subtracted from the RFU of the EV incubation. (a) Kinetics of ADAM17 activity in ascites‐EV, one representative of three biological replicates is shown. (b) Mean RFU (endpoint) of the cleavage product of three biological replicates + SEM is displayed. Based on the Shapiro–Wilk normality test, statistical significance was analysed by RM one‐way‐ANOVA following Tukey's multiple comparison test. * p < 0.05, ** p < 0.01.
Quenched Fluorogenic Peptide Substrate Abz–Leu–Ala–Gln–Ala–Val–Arg–Ser–Ser–Ser–Arg–Dap(dnp)–Nh2, supplied by Biozol Diagnostica Vertrieb 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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Thermo Fisher nuclear fluorogen 4 6 diamidino 2 phenylindole dapi
ADAM17 is proteolytically active on isolated ascites‐EV. ADAM17 proteolytic activity of ascites‐EV was quantified using a cell‐free ADAM17 activity assay. 1 × 10 9 ascites‐EV of three OvCa patients (#1, #2 and #3) or PBS as a control were incubated at 37°C for 80 min with a <t>fluorogenic</t> substrate. Relative fluorescence units (RFU) were measured every 30 s. RFU of the PBS control was subtracted from the RFU of the EV incubation. (a) Kinetics of ADAM17 activity in ascites‐EV, one representative of three biological replicates is shown. (b) Mean RFU (endpoint) of the cleavage product of three biological replicates + SEM is displayed. Based on the Shapiro–Wilk normality test, statistical significance was analysed by RM one‐way‐ANOVA following Tukey's multiple comparison test. * p < 0.05, ** p < 0.01.
Nuclear Fluorogen 4 6 Diamidino 2 Phenylindole Dapi, supplied by Thermo Fisher, 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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Fisher Scientific dapi
ADAM17 is proteolytically active on isolated ascites‐EV. ADAM17 proteolytic activity of ascites‐EV was quantified using a cell‐free ADAM17 activity assay. 1 × 10 9 ascites‐EV of three OvCa patients (#1, #2 and #3) or PBS as a control were incubated at 37°C for 80 min with a <t>fluorogenic</t> substrate. Relative fluorescence units (RFU) were measured every 30 s. RFU of the PBS control was subtracted from the RFU of the EV incubation. (a) Kinetics of ADAM17 activity in ascites‐EV, one representative of three biological replicates is shown. (b) Mean RFU (endpoint) of the cleavage product of three biological replicates + SEM is displayed. Based on the Shapiro–Wilk normality test, statistical significance was analysed by RM one‐way‐ANOVA following Tukey's multiple comparison test. * p < 0.05, ** p < 0.01.
Dapi, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Merck KGaA fluorogenic substrate mca-lys-pro-leu-gly-leu-dap(dnp)-ala-arg-nh2
ADAM17 is proteolytically active on isolated ascites‐EV. ADAM17 proteolytic activity of ascites‐EV was quantified using a cell‐free ADAM17 activity assay. 1 × 10 9 ascites‐EV of three OvCa patients (#1, #2 and #3) or PBS as a control were incubated at 37°C for 80 min with a <t>fluorogenic</t> substrate. Relative fluorescence units (RFU) were measured every 30 s. RFU of the PBS control was subtracted from the RFU of the EV incubation. (a) Kinetics of ADAM17 activity in ascites‐EV, one representative of three biological replicates is shown. (b) Mean RFU (endpoint) of the cleavage product of three biological replicates + SEM is displayed. Based on the Shapiro–Wilk normality test, statistical significance was analysed by RM one‐way‐ANOVA following Tukey's multiple comparison test. * p < 0.05, ** p < 0.01.
Fluorogenic Substrate Mca Lys Pro Leu Gly Leu Dap(dnp) Ala Arg Nh2, supplied by Merck KGaA, 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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Biosynth Carbosynth mmp 13 specific fluorogenic substrate mocac pro cha gly nva his ala dap dnp nh 2
ADAM17 is proteolytically active on isolated ascites‐EV. ADAM17 proteolytic activity of ascites‐EV was quantified using a cell‐free ADAM17 activity assay. 1 × 10 9 ascites‐EV of three OvCa patients (#1, #2 and #3) or PBS as a control were incubated at 37°C for 80 min with a <t>fluorogenic</t> substrate. Relative fluorescence units (RFU) were measured every 30 s. RFU of the PBS control was subtracted from the RFU of the EV incubation. (a) Kinetics of ADAM17 activity in ascites‐EV, one representative of three biological replicates is shown. (b) Mean RFU (endpoint) of the cleavage product of three biological replicates + SEM is displayed. Based on the Shapiro–Wilk normality test, statistical significance was analysed by RM one‐way‐ANOVA following Tukey's multiple comparison test. * p < 0.05, ** p < 0.01.
Mmp 13 Specific Fluorogenic Substrate Mocac Pro Cha Gly Nva His Ala Dap Dnp Nh 2, supplied by Biosynth Carbosynth, 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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Image Search Results


Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with DAPI.

Journal: Water

Article Title: Effects of Underwater Lighting Time on the Growth of Vallisneria spinulosa Yan and Its Water Restoration Process

doi: 10.3390/w16243697

Figure Lengend Snippet: Figure 6. CLSM diagram of leaf–biofilm complex in different light duration ratios. (a) LV: V. spin- ulosa + low light duration ratio, (b) MV: V. spinulosa + medium light duration ratio, and (c) HV: V. spinulosa + high light duration ratio. Red is EPS polysaccharide stained with Texas red, green is protein stained with FITC, and bright blue is DNA stained with DAPI.

Article Snippet: CLSM Determination Plant leaves were collected and cut into small pieces of 5 mm × 5 mm and then placed in a 24−well microplate containing 2.5% glutaraldehyde (0.1 M PBS, pH = 7.2) phosphate buffer for 24 h. After washing 3–5 times with 0.1 M PBS solution (pH = 7.2) (Shanghai Macklin Biochemical Technology Co., Ltd., Shanghai, China), the DNA, extracellular polysaccharides, and proteins were labeled with the fluorescent dyes DAPI, Con A−Texas red conjugate solution (Invitrogen, San Diego, CA, USA), and FITC (Shanghai Macklin Biochemical Technology Co., Ltd., Shanghai, China), respectively.

Techniques: Staining

ADAM17 is proteolytically active on isolated ascites‐EV. ADAM17 proteolytic activity of ascites‐EV was quantified using a cell‐free ADAM17 activity assay. 1 × 10 9 ascites‐EV of three OvCa patients (#1, #2 and #3) or PBS as a control were incubated at 37°C for 80 min with a fluorogenic substrate. Relative fluorescence units (RFU) were measured every 30 s. RFU of the PBS control was subtracted from the RFU of the EV incubation. (a) Kinetics of ADAM17 activity in ascites‐EV, one representative of three biological replicates is shown. (b) Mean RFU (endpoint) of the cleavage product of three biological replicates + SEM is displayed. Based on the Shapiro–Wilk normality test, statistical significance was analysed by RM one‐way‐ANOVA following Tukey's multiple comparison test. * p < 0.05, ** p < 0.01.

Journal: Journal of Extracellular Vesicles

Article Title: Chemotherapy‐induced release of ADAM17 bearing EV as a potential resistance mechanism in ovarian cancer

doi: 10.1002/jev2.12338

Figure Lengend Snippet: ADAM17 is proteolytically active on isolated ascites‐EV. ADAM17 proteolytic activity of ascites‐EV was quantified using a cell‐free ADAM17 activity assay. 1 × 10 9 ascites‐EV of three OvCa patients (#1, #2 and #3) or PBS as a control were incubated at 37°C for 80 min with a fluorogenic substrate. Relative fluorescence units (RFU) were measured every 30 s. RFU of the PBS control was subtracted from the RFU of the EV incubation. (a) Kinetics of ADAM17 activity in ascites‐EV, one representative of three biological replicates is shown. (b) Mean RFU (endpoint) of the cleavage product of three biological replicates + SEM is displayed. Based on the Shapiro–Wilk normality test, statistical significance was analysed by RM one‐way‐ANOVA following Tukey's multiple comparison test. * p < 0.05, ** p < 0.01.

Article Snippet: The enzymatic activity of ADAM17 on EV was analysed using a commercially available quenched fluorogenic peptide substrate (Abz‐Leu‐Ala‐Gln‐Ala‐Val‐Arg‐Ser‐ser‐Ser‐Arg‐Dap(DNP)‐NH2) (Biozol, #BYT‐ORB104351).

Techniques: Isolation, Activity Assay, Control, Incubation, Fluorescence, Comparison