antibody absorption Search Results


absorptive enterocytes  (Biorbyt)
91
Biorbyt absorptive enterocytes
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Absorptive Enterocytes, supplied by Biorbyt, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescent treponemal antibody absorption testing glass slides  (ZEUS Scientific)
90
ZEUS Scientific fluorescent treponemal antibody absorption testing glass slides
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption Testing Glass Slides, supplied by ZEUS Scientific, 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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fluorescent treponemal antibody absorption (fta-abs) test  (MarDx Diagnostics Inc)
90
MarDx Diagnostics Inc fluorescent treponemal antibody absorption (fta-abs) test
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption (Fta Abs) Test, supplied by MarDx Diagnostics 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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fluorescent treponemal antibody absorption test fta-abs  (Mast Diagnostica GmbH)
90
Mast Diagnostica GmbH fluorescent treponemal antibody absorption test fta-abs
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption Test Fta Abs, supplied by Mast Diagnostica 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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fluorescent treponemal antibody absorption (fta-abs) t. pallidum -igg  (EUROIMMUN)
90
EUROIMMUN fluorescent treponemal antibody absorption (fta-abs) t. pallidum -igg
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption (Fta Abs) T. Pallidum Igg, supplied by EUROIMMUN, 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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fluorescent treponemal antibody-absorption test (fta-abs)  (Trinity Biotech)
90
Trinity Biotech fluorescent treponemal antibody-absorption test (fta-abs)
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption Test (Fta Abs), supplied by Trinity Biotech, 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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fluorescent treponemal antibody absorption (fta-abs) test  (Becton Dickinson)
90
Becton Dickinson fluorescent treponemal antibody absorption (fta-abs) test
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption (Fta Abs) Test, supplied by Becton Dickinson, 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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fluorescent treponemal antibody absorption test (fta-abs)  (Reagen LLC)
90
Reagen LLC fluorescent treponemal antibody absorption test (fta-abs)
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption Test (Fta Abs), supplied by Reagen LLC, 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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fluorescent treponemal antibody absorption test  (Johns Hopkins HealthCare)
90
Johns Hopkins HealthCare fluorescent treponemal antibody absorption test
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption Test, supplied by Johns Hopkins HealthCare, 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/antibody+absorption/fluorescent+treponemal+antibody+absorption+test/pm09677171-153-14-8
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fluorescent treponemal antibody absorption test igm  (Scimedx Inc)
90
Scimedx Inc fluorescent treponemal antibody absorption test igm
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Fluorescent Treponemal Antibody Absorption Test Igm, supplied by Scimedx 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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im absorption test for heterphil antibody  (Microgen Bioproducts)
90
Microgen Bioproducts im absorption test for heterphil antibody
The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % <t>enterocytes</t> or <t>absorptive</t> surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).
Im Absorption Test For Heterphil Antibody, supplied by Microgen Bioproducts, 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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anti-gut absorptive cell epitopes monoclonal antibody, clone hks6d9/3  (Creative BioMart)
N/A
Shipped at 4°C. Upon delivery aliquot and store at-20°C or-80°C. Avoid repeated freeze / thaw cycles.http://www.creative-diagnostics.com/Anti-Zebrafish-Gut-Absorptive-Cell-Epitopes-Antibody-130546-144.htm
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Image Search Results


The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % enterocytes or absorptive surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).

Journal: Journal of toxicology and environmental health. Part A

Article Title: Embryonic Arsenic Exposure Reduces Intestinal Cell Proliferation and Alters Hepatic IGF mRNA Expression in Killifish ( Fundulus heteroclitus )

doi: 10.1080/15287394.2019.1571465

Figure Lengend Snippet: The number of proliferating cells in anterior intestine in embryonically-exposed killifish. Immunohistochemistry was used to examine the number of proliferating cells as measured by nuclear staining of PCNA (A; indicated by arrows), the number of goblet cells (B; indicated by arrows), and % enterocytes or absorptive surface (B) (representative images are shown of n = 6 fish per exposure group per time point). The number of PCNA+ cells were counted per 2 intervillus regions at a 40X field of view, and averaged per villus (C). Absorptive surface area was quantified by outlining 4 villi per field of view at 10X for absorptive surface and determining % stained cells using ImageJ (D). Goblet cells were counted from 4 villi per field of view at 10X, and averaged per villus (E). The colors were converted to a black and white image so only cytoplasmic staining of the enterocytes would be determined. All sections were averaged per group, and statistical significance (*) was determined by ANOVA followed by Tukey’s (p < 0.05).

Article Snippet: Paraffin embedded intestinal sections (7 μm) were examined for markers of absorptive enterocytes (gut absorptive cell epitope antibody; Biorbyt, # orb324078), while the number of proliferating cells was determined by expression of proliferating cell nuclear antigen (PCNA) (Abcam, #ab29).

Techniques: Immunohistochemistry, Staining