image analysis software multi gauge version 3.0 (FUJIFILM)
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FUJIFILM
image analysis software multi gauge version 3.0
Image Analysis Software Multi Gauge Version 3.0, supplied by FUJIFILM, 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/product/image+analysis+software+multi+gauge+version+3%2E0/multi+gauge+software/pm38104746-84-6-13
Average 90 stars, based on 1 article reviews
Image Analysis Software Multi Gauge Version 3.0, supplied by FUJIFILM, 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/product/image+analysis+software+multi+gauge+version+3%2E0/multi+gauge+software/pm38104746-84-6-13
Average 90 stars, based on 1 article reviews
image analysis software multi gauge version 3.0 - by Bioz Stars,
2026-09
90/100 stars
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Related Articles
Binding Assay:Article Title: Heat stress upregulates G-T mismatch binding activities in zebrafish (Danio rerio) embryos preexposed and nonexposed to a sublethal level of cadmium (Cd). Article Snippet: Accepted Manuscript Heat stress upregulates G-T mismatch binding activities in zebrafishDanio rerio embryos preexposed and nonexposed to a sublethal level of cadmium (Cd) Tsung-Nan Ho, Ganjai Vikram Paul, Yen-Hung Chen, Todd Hsu PII: S0045-6535(18)32135-0 DOI: 10.1016/j.chemosphere.2018.11.038 Reference: CHEM 22522 To appear in: Chemosphere Received Date: 26 June 2018 Accepted Date: 04 November 2018 Please cite this article as: Tsung-Nan Ho, Ganjai Vikram Paul, Yen-Hung Chen, Todd Hsu, Heat stress upregulates G-T mismatch binding activities in zebrafishembryos preexposed Danio rerio and nonexposed to a sublethal level of cadmium (Cd), (2018), doi: 10.1016/j.Chemosphere chemosphere.2018.11.038 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Article Title: Oxidative stress intensity-related effects of cadmium (Cd) and paraquat (PQ) on UV-damaged-DNA binding and excision repair activities in zebrafish (Danio rerio) embryos. Article Snippet: Our earlier studies showed the inhibitory effects of cadmium (Cd) and paraquat (PQ) on the gene expression of DNA mismatch recognition proteins in zebrafish (Danio rerio) embryos.. This study explored the effects of Cd and PQ on nucleotide excision repair (NER) capacity in zebrafish embryos.. Exposure of embryos at 1 h post fertilization (hpf) to 3e5 mM Cd or 30e100 mM PQ for 9 h induced a 2e3-fold increase of oxidative stress, while a 6.5-fold increase of oxidative stress was induced by 200 mM PQ. Article Title: Aluminum (Al) causes a delayed suppression of nucleotide excision repair (NER) capacity in zebrafish (Danio rerio) embryos via disturbance of DNA lesion detection. Article Snippet: Aluminum (Al) is extensively used for making cooking utensils and its presence in the aquatic environment may occur through acid mine drainage and wastewater discharge.. Al is known to induce genotoxicity in human cells, rodents, and fish.. Nucleotide excision repair (NER) eliminates helix-twisting DNA lesions such as UV-induced dipyrimidine photoproducts. Article Title: Thallium(I) induces a prolonged inhibition of (6-4)photoproduct binding and UV damage excision repair activities in zebrafish (Danio rerio) embryos via protein inactivation. Article Snippet: Cyclobutane pyrimidine dimer (CPD) and (6-4)photoproduct (6-4 PP) are two major types of UV-induced DNA lesion and 6-4 PP is more mutagenic than CPD.. Activated by lesion detection, nucleotide excision repair (NER) eliminates CPDs and 6-4 PPs.. Thallium (Tl) is a toxic metal existing primarily as Tl in the aquatic environment. Software:Article Title: Heat stress upregulates G-T mismatch binding activities in zebrafish (Danio rerio) embryos preexposed and nonexposed to a sublethal level of cadmium (Cd). Article Snippet: Accepted Manuscript Heat stress upregulates G-T mismatch binding activities in zebrafishDanio rerio embryos preexposed and nonexposed to a sublethal level of cadmium (Cd) Tsung-Nan Ho, Ganjai Vikram Paul, Yen-Hung Chen, Todd Hsu PII: S0045-6535(18)32135-0 DOI: 10.1016/j.chemosphere.2018.11.038 Reference: CHEM 22522 To appear in: Chemosphere Received Date: 26 June 2018 Accepted Date: 04 November 2018 Please cite this article as: Tsung-Nan Ho, Ganjai Vikram Paul, Yen-Hung Chen, Todd Hsu, Heat stress upregulates G-T mismatch binding activities in zebrafishembryos preexposed Danio rerio and nonexposed to a sublethal level of cadmium (Cd), (2018), doi: 10.1016/j.Chemosphere chemosphere.2018.11.038 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Article Title: Evaluation method for cell-free in situ tissue-engineered vasculature monitoring: Proof of growth and development in a canine IVC model. Article Snippet: Sample immunoblots were incubated with antibodies against the following targets: α-SMA (1:1000, clone 1A4; Dako), MYH11 (1:1000, ab53219; Abcam), and desmin (1:1000, RD-301; ThermoFisher Scientific, Rockford, IL) or vimentin (1:2000, ab8069; Abcam) to detect three blots simultaneously on the same lane. .. Membranes were treated with a chemiluminescent reagent (Western BLoT Sensitive HRP Substrate; Takara) for enhancement, followed by analysis of blot images using a cooled charge-coupled device camera (Las 3000 Mini; Fujifilm, Tokyo, Japan) and Article Title: Oxidative stress intensity-related effects of cadmium (Cd) and paraquat (PQ) on UV-damaged-DNA binding and excision repair activities in zebrafish (Danio rerio) embryos. Article Snippet: Our earlier studies showed the inhibitory effects of cadmium (Cd) and paraquat (PQ) on the gene expression of DNA mismatch recognition proteins in zebrafish (Danio rerio) embryos.. This study explored the effects of Cd and PQ on nucleotide excision repair (NER) capacity in zebrafish embryos.. Exposure of embryos at 1 h post fertilization (hpf) to 3e5 mM Cd or 30e100 mM PQ for 9 h induced a 2e3-fold increase of oxidative stress, while a 6.5-fold increase of oxidative stress was induced by 200 mM PQ. Article Title: Identification of low-molecular-weight vitellogenin 1 (Vg1)-like proteins as nucleotide excision repair (NER) factors in developing zebrafish (Danio rerio) using a transcription-based DNA repair assay. Article Snippet: Nucleotide excision repair (NER) removes helix-distorting DNA lesions such as UV-induced pyrimidine dimers and cisplatin-induced strand crosslinking.. Our earlier studies have identified lowmolecular-weight proteins homologous to the 150-kDa vitellogenin 1 (Vg1) as UV-damaged DNA-binding factors expressed in developing zebrafish (Danio rerio).. This present study explored if Vg1-like proteins also participated in NER in zebrafish. Article Title: Aluminum (Al) causes a delayed suppression of nucleotide excision repair (NER) capacity in zebrafish (Danio rerio) embryos via disturbance of DNA lesion detection. Article Snippet: Aluminum (Al) is extensively used for making cooking utensils and its presence in the aquatic environment may occur through acid mine drainage and wastewater discharge.. Al is known to induce genotoxicity in human cells, rodents, and fish.. Nucleotide excision repair (NER) eliminates helix-twisting DNA lesions such as UV-induced dipyrimidine photoproducts. Article Title: Thallium(I) induces a prolonged inhibition of (6-4)photoproduct binding and UV damage excision repair activities in zebrafish (Danio rerio) embryos via protein inactivation. Article Snippet: Cyclobutane pyrimidine dimer (CPD) and (6-4)photoproduct (6-4 PP) are two major types of UV-induced DNA lesion and 6-4 PP is more mutagenic than CPD.. Activated by lesion detection, nucleotide excision repair (NER) eliminates CPDs and 6-4 PPs.. Thallium (Tl) is a toxic metal existing primarily as Tl in the aquatic environment. Article Title: Heat stress modulates nucleotide excision repair capacity in zebrafish (Danio rerio) early and mid-early embryos via distinct mechanisms. Article Snippet: Discharge of heated effluent at 8e12 C above ambient into water areas is known to retard the growth of aquatic organisms due to heat stress.. Nucleotide excision repair (NER) maintains genome integrity by removing helix-distorting adducts such as UV-induced DNA lesions.. This study explored how NER in zebrafish (Danio rerio) embryos at different hours post fertilization (hpf) responded to þ 8.5 C heat shock for 30 min. Our transcription-based repair assay monitoring the ability of zebrafish extracts to upregulate a UV-suppressed gene expression detected a 2-fold increase of NER capacity in 10 hpf early embryos after heat stress. Article Title: Mercury (II) impairs nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos by targeting primarily at the stage of DNA incision. Article Snippet: Mercuric ion (Hg) is the most prevalent form of inorganic Hg found in polluted aquatic environment.. As inhibition of DNA damage repair has been proposed as one of the mechanisms of Hg-induced genotoxicity in aquatic animals and mammalian cells, this study explored the susceptibility of different stages of nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos to Hg using UV-damaged DNA as the repair substrate.. Exposure of embryos at 1 h post fertilization (hpf) to HgCl2 at 0.1–2.5 μM for 9 h caused a concentration-dependent inhibition of NER capacity monitored by a transcription-based DNA repair assay. Western Blot:Article Title: Evaluation method for cell-free in situ tissue-engineered vasculature monitoring: Proof of growth and development in a canine IVC model. Article Snippet: Sample immunoblots were incubated with antibodies against the following targets: α-SMA (1:1000, clone 1A4; Dako), MYH11 (1:1000, ab53219; Abcam), and desmin (1:1000, RD-301; ThermoFisher Scientific, Rockford, IL) or vimentin (1:2000, ab8069; Abcam) to detect three blots simultaneously on the same lane. .. Membranes were treated with a chemiluminescent reagent (Western BLoT Sensitive HRP Substrate; Takara) for enhancement, followed by analysis of blot images using a cooled charge-coupled device camera (Las 3000 Mini; Fujifilm, Tokyo, Japan) and Plasmid Preparation:Article Title: Oxidative stress intensity-related effects of cadmium (Cd) and paraquat (PQ) on UV-damaged-DNA binding and excision repair activities in zebrafish (Danio rerio) embryos. Article Snippet: Our earlier studies showed the inhibitory effects of cadmium (Cd) and paraquat (PQ) on the gene expression of DNA mismatch recognition proteins in zebrafish (Danio rerio) embryos.. This study explored the effects of Cd and PQ on nucleotide excision repair (NER) capacity in zebrafish embryos.. Exposure of embryos at 1 h post fertilization (hpf) to 3e5 mM Cd or 30e100 mM PQ for 9 h induced a 2e3-fold increase of oxidative stress, while a 6.5-fold increase of oxidative stress was induced by 200 mM PQ. Article Title: Identification of low-molecular-weight vitellogenin 1 (Vg1)-like proteins as nucleotide excision repair (NER) factors in developing zebrafish (Danio rerio) using a transcription-based DNA repair assay. Article Snippet: Nucleotide excision repair (NER) removes helix-distorting DNA lesions such as UV-induced pyrimidine dimers and cisplatin-induced strand crosslinking.. Our earlier studies have identified lowmolecular-weight proteins homologous to the 150-kDa vitellogenin 1 (Vg1) as UV-damaged DNA-binding factors expressed in developing zebrafish (Danio rerio).. This present study explored if Vg1-like proteins also participated in NER in zebrafish. Article Title: Mercury (II) impairs nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos by targeting primarily at the stage of DNA incision. Article Snippet: Mercuric ion (Hg) is the most prevalent form of inorganic Hg found in polluted aquatic environment.. As inhibition of DNA damage repair has been proposed as one of the mechanisms of Hg-induced genotoxicity in aquatic animals and mammalian cells, this study explored the susceptibility of different stages of nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos to Hg using UV-damaged DNA as the repair substrate.. Exposure of embryos at 1 h post fertilization (hpf) to HgCl2 at 0.1–2.5 μM for 9 h caused a concentration-dependent inhibition of NER capacity monitored by a transcription-based DNA repair assay. Activity Assay:Article Title: Aluminum (Al) causes a delayed suppression of nucleotide excision repair (NER) capacity in zebrafish (Danio rerio) embryos via disturbance of DNA lesion detection. Article Snippet: Aluminum (Al) is extensively used for making cooking utensils and its presence in the aquatic environment may occur through acid mine drainage and wastewater discharge.. Al is known to induce genotoxicity in human cells, rodents, and fish.. Nucleotide excision repair (NER) eliminates helix-twisting DNA lesions such as UV-induced dipyrimidine photoproducts. Article Title: Mercury (II) impairs nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos by targeting primarily at the stage of DNA incision. Article Snippet: Mercuric ion (Hg) is the most prevalent form of inorganic Hg found in polluted aquatic environment.. As inhibition of DNA damage repair has been proposed as one of the mechanisms of Hg-induced genotoxicity in aquatic animals and mammalian cells, this study explored the susceptibility of different stages of nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos to Hg using UV-damaged DNA as the repair substrate.. Exposure of embryos at 1 h post fertilization (hpf) to HgCl2 at 0.1–2.5 μM for 9 h caused a concentration-dependent inhibition of NER capacity monitored by a transcription-based DNA repair assay. Generated:Article Title: Aluminum (Al) causes a delayed suppression of nucleotide excision repair (NER) capacity in zebrafish (Danio rerio) embryos via disturbance of DNA lesion detection. Article Snippet: Aluminum (Al) is extensively used for making cooking utensils and its presence in the aquatic environment may occur through acid mine drainage and wastewater discharge.. Al is known to induce genotoxicity in human cells, rodents, and fish.. Nucleotide excision repair (NER) eliminates helix-twisting DNA lesions such as UV-induced dipyrimidine photoproducts. Electrophoretic Mobility Shift Assay:Article Title: Heat stress modulates nucleotide excision repair capacity in zebrafish (Danio rerio) early and mid-early embryos via distinct mechanisms. Article Snippet: Discharge of heated effluent at 8e12 C above ambient into water areas is known to retard the growth of aquatic organisms due to heat stress.. Nucleotide excision repair (NER) maintains genome integrity by removing helix-distorting adducts such as UV-induced DNA lesions.. This study explored how NER in zebrafish (Danio rerio) embryos at different hours post fertilization (hpf) responded to þ 8.5 C heat shock for 30 min. Our transcription-based repair assay monitoring the ability of zebrafish extracts to upregulate a UV-suppressed gene expression detected a 2-fold increase of NER capacity in 10 hpf early embryos after heat stress. Marker:Article Title: Mercury (II) impairs nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos by targeting primarily at the stage of DNA incision. Article Snippet: Mercuric ion (Hg) is the most prevalent form of inorganic Hg found in polluted aquatic environment.. As inhibition of DNA damage repair has been proposed as one of the mechanisms of Hg-induced genotoxicity in aquatic animals and mammalian cells, this study explored the susceptibility of different stages of nucleotide excision repair (NER) in zebrafish (Danio rerio) embryos to Hg using UV-damaged DNA as the repair substrate.. Exposure of embryos at 1 h post fertilization (hpf) to HgCl2 at 0.1–2.5 μM for 9 h caused a concentration-dependent inhibition of NER capacity monitored by a transcription-based DNA repair assay. |