metamorph 6.1. software Search Results


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universal imaging inc metamorph software version 6.1
Metamorph Software Version 6.1, supplied by universal imaging 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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MetaMorph Inc 4.5 imaging software
4.5 Imaging Software, supplied by MetaMorph 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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MetaMorph Inc 7.0 image analysis software
7.0 Image Analysis Software, supplied by MetaMorph 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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MetaMorph Inc image analysis software version 6.1
Image Analysis Software Version 6.1, supplied by MetaMorph 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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MetaMorph Inc acquision software
Acquision Software, supplied by MetaMorph 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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MetaMorph Inc software metamorph v.6.1
Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of <t>DHE</t> expression was determined ( E ) with <t>the</t> <t>software</t> MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.
Software Metamorph V.6.1, supplied by MetaMorph 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/software metamorph v.6.1/product/MetaMorph Inc
Average 90 stars, based on 1 article reviews
software metamorph v.6.1 - by Bioz Stars, 2026-04
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MetaMorph Inc 6.1 analysis software
Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of <t>DHE</t> expression was determined ( E ) with <t>the</t> <t>software</t> MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.
6.1 Analysis Software, supplied by MetaMorph 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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MetaMorph Inc computer-based software metamorph 6.1
Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of <t>DHE</t> expression was determined ( E ) with <t>the</t> <t>software</t> MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.
Computer Based Software Metamorph 6.1, supplied by MetaMorph 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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MetaMorph Inc v 6.1 software
Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of <t>DHE</t> expression was determined ( E ) with <t>the</t> <t>software</t> MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.
V 6.1 Software, supplied by MetaMorph 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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MetaMorph Inc microangiometer using metamorph 6.1 software
Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of <t>DHE</t> expression was determined ( E ) with <t>the</t> <t>software</t> MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.
Microangiometer Using Metamorph 6.1 Software, supplied by MetaMorph 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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MetaMorph Inc hsi color model of the set color threshold subroutine of metamorph 6.1 software
Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of <t>DHE</t> expression was determined ( E ) with <t>the</t> <t>software</t> MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.
Hsi Color Model Of The Set Color Threshold Subroutine Of Metamorph 6.1 Software, supplied by MetaMorph 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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MetaMorph Inc pixel intensity quantitation using metamorph 6.1 software
Quantitation of fertilization-induced changes in calcium <t>green</t> <t>fluorescence.</t> Oocytes were injected with calcium green dextran and GST, then images were recorded after a 10-min recovery period. Fertilization was initiated by addition of a mixture of sperm and water at time 0 and images were recorded every 15 s. Fluorescence was quantitated by pixel intensity quantitation using Metamorph <t>6.1</t> software. The top panel represents global fluorescence measured from a cross-section of the entire zygote. The middle panel represent fluorescence measured within a circular region in the center of the zygote (central cytoplasm) comprising approximately 25% of the total cross-sectional area. The bottom panel represents fluorescence measured within an arc traced over the cortex (cortical cytoplasm) as near as possible to the micropyle. This arc comprised approximately 20% of the perimeter of the zygote.
Pixel Intensity Quantitation Using Metamorph 6.1 Software, supplied by MetaMorph 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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pixel intensity quantitation using metamorph 6.1 software - by Bioz Stars, 2026-04
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Image Search Results


Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of DHE expression was determined ( E ) with the software MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.

Journal: Scientific Reports

Article Title: Effect of Cucumis sativus on Dysfunctional 3T3-L1 Adipocytes

doi: 10.1038/s41598-019-49458-6

Figure Lengend Snippet: Superoxide induction by IL-1β in 3T3-L1 adipocytes. Mature adipocytes (day 8) were cultured for 24, 48, 60, or 72 h, either alone, with IL-1β, and/or insulin 1 μM. Microphotographs were taken in a spectrofluorometer under a 20X objective at 24 ( A ), 48 ( B ), 60 ( C ), and 72 h ( D ). The percent of DHE expression was determined ( E ) with the software MetaMorph v.6.1. Results are expressed as mean ± SD, *P ≤ 0.05 with respect to cells treated with insulin 1 μM and were analyzed by ANOVA and the post-hoc Tukey-Kramer test, n = 6.

Article Snippet: The percent of DHE expression was determined ( E ) with the software MetaMorph v.6.1.

Techniques: Cell Culture, Expressing, Software

Quantitation of fertilization-induced changes in calcium green fluorescence. Oocytes were injected with calcium green dextran and GST, then images were recorded after a 10-min recovery period. Fertilization was initiated by addition of a mixture of sperm and water at time 0 and images were recorded every 15 s. Fluorescence was quantitated by pixel intensity quantitation using Metamorph 6.1 software. The top panel represents global fluorescence measured from a cross-section of the entire zygote. The middle panel represent fluorescence measured within a circular region in the center of the zygote (central cytoplasm) comprising approximately 25% of the total cross-sectional area. The bottom panel represents fluorescence measured within an arc traced over the cortex (cortical cytoplasm) as near as possible to the micropyle. This arc comprised approximately 20% of the perimeter of the zygote.

Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Analysis of Signaling Pathways in Zebrafish Development by Microinjection

doi: 10.1007/978-1-59745-202-1_6

Figure Lengend Snippet: Quantitation of fertilization-induced changes in calcium green fluorescence. Oocytes were injected with calcium green dextran and GST, then images were recorded after a 10-min recovery period. Fertilization was initiated by addition of a mixture of sperm and water at time 0 and images were recorded every 15 s. Fluorescence was quantitated by pixel intensity quantitation using Metamorph 6.1 software. The top panel represents global fluorescence measured from a cross-section of the entire zygote. The middle panel represent fluorescence measured within a circular region in the center of the zygote (central cytoplasm) comprising approximately 25% of the total cross-sectional area. The bottom panel represents fluorescence measured within an arc traced over the cortex (cortical cytoplasm) as near as possible to the micropyle. This arc comprised approximately 20% of the perimeter of the zygote.

Article Snippet: Fertilization was initiated by addition of a mixture of sperm and water at time 0 and images were recorded every 15 s. Fluorescence was quantitated by pixel intensity quantitation using Metamorph 6.1 software.

Techniques: Quantitation Assay, Fluorescence, Injection, Software