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Danaher Inc anti ubiquitin carboxyl terminal hydrolase isozyme l1 uchl1 rabbit polyclonal antibody
Anti Ubiquitin Carboxyl Terminal Hydrolase Isozyme L1 Uchl1 Rabbit Polyclonal Antibody, supplied by Danaher Inc, 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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Rockland Immunochemicals superoxide dismutase rabbit
Impact of adropin on <t>superoxide</t> <t>dismutase</t> expression in pancreatic β‐cells of normoglycemic and diabetic rats. (A) Immunofluorescence labeling with anti‐superoxide dismutase antibody and anti‐insulin antibodies showed expression of superoxide dismutase in pancreatic β‐cells. (B) Quantification of the histological analysis showed a significant (*** p < 0.001) decrease in superoxide dismutase distribution in pancreatic endocrine cells and a significant (**** p < 0.0001) decrease in its localization in β‐cells of rats with diabetes when compared to the normal group. n = 6. Scale bar: 50 μm. Data analysis was done using the ANOVA test.
Superoxide Dismutase Rabbit, supplied by Rockland Immunochemicals, 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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Elabscience Biotechnology colorimetric detection card by afb1
Impact of adropin on <t>superoxide</t> <t>dismutase</t> expression in pancreatic β‐cells of normoglycemic and diabetic rats. (A) Immunofluorescence labeling with anti‐superoxide dismutase antibody and anti‐insulin antibodies showed expression of superoxide dismutase in pancreatic β‐cells. (B) Quantification of the histological analysis showed a significant (*** p < 0.001) decrease in superoxide dismutase distribution in pancreatic endocrine cells and a significant (**** p < 0.0001) decrease in its localization in β‐cells of rats with diabetes when compared to the normal group. n = 6. Scale bar: 50 μm. Data analysis was done using the ANOVA test.
Colorimetric Detection Card By Afb1, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Elabscience Biotechnology rapid test kit
Impact of adropin on <t>superoxide</t> <t>dismutase</t> expression in pancreatic β‐cells of normoglycemic and diabetic rats. (A) Immunofluorescence labeling with anti‐superoxide dismutase antibody and anti‐insulin antibodies showed expression of superoxide dismutase in pancreatic β‐cells. (B) Quantification of the histological analysis showed a significant (*** p < 0.001) decrease in superoxide dismutase distribution in pancreatic endocrine cells and a significant (**** p < 0.0001) decrease in its localization in β‐cells of rats with diabetes when compared to the normal group. n = 6. Scale bar: 50 μm. Data analysis was done using the ANOVA test.
Rapid Test Kit, supplied by Elabscience Biotechnology, 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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Elabscience Biotechnology t 2 t 2 toxin lateral flow assay kit elabscience inc
Commercially available rapid diagnostic tools for the detection of T-2/HT-2 in cereals.
T 2 T 2 Toxin Lateral Flow Assay Kit Elabscience Inc, supplied by Elabscience Biotechnology, 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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Boster Bio elisa kits
Commercially available rapid diagnostic tools for the detection of T-2/HT-2 in cereals.
Elisa Kits, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Elabscience Biotechnology avian influenza virus h5n1 antigen lateral flow assay kit
Commercially available rapid diagnostic tools for the detection of T-2/HT-2 in cereals.
Avian Influenza Virus H5n1 Antigen Lateral Flow Assay Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Elabscience Biotechnology albuterol salbutamol
Figure 3. Comparison of LFA outputs versus <t>albuterol</t> concentration (ppb) for selected urine simu- lants. Aggregated LFA readout values from all urine simulants (n = 9) (A), from concentrated urine simulant (B), high salt only urine simulant, (C) and dilute urine simulant (D).
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Elabscience Biotechnology e ad c063
Figure 3. Comparison of LFA outputs versus <t>albuterol</t> concentration (ppb) for selected urine simu- lants. Aggregated LFA readout values from all urine simulants (n = 9) (A), from concentrated urine simulant (B), high salt only urine simulant, (C) and dilute urine simulant (D).
E Ad C063, supplied by Elabscience Biotechnology, 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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Elabscience Biotechnology rabies virus antigen rapid test kit
Figure 3. Comparison of LFA outputs versus <t>albuterol</t> concentration (ppb) for selected urine simu- lants. Aggregated LFA readout values from all urine simulants (n = 9) (A), from concentrated urine simulant (B), high salt only urine simulant, (C) and dilute urine simulant (D).
Rabies Virus Antigen Rapid Test Kit, supplied by Elabscience Biotechnology, 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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Novus Biologicals intracellular staining flow assay kit
Figure 1. Expression of TLR-1, -5, and -9 on T lymphocytes and monocytes. Histogram plots of TLR-1, -5, and -9 expression in a patient with aGVHD and in a patient without aGVHD. The expression of surface (TLR-1 and -5) and <t>intracellular</t> (TLR-9) TLRs is reported with the corresponding negative control (mouse IgG1-PE). MFI is shown for each histogram. T lymphocytes of the patient with aGVHD have higher MFI values of TLR-5 and lower MFI values of TLR-1 and -9 compared with the patient without aGVHD (A). An analogous TLR profile is displayed by monocytes (B).
Intracellular Staining Flow Assay Kit, supplied by Novus Biologicals, 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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Arthrex Inc lateral decubitus anchors
Figure 1. Expression of TLR-1, -5, and -9 on T lymphocytes and monocytes. Histogram plots of TLR-1, -5, and -9 expression in a patient with aGVHD and in a patient without aGVHD. The expression of surface (TLR-1 and -5) and <t>intracellular</t> (TLR-9) TLRs is reported with the corresponding negative control (mouse IgG1-PE). MFI is shown for each histogram. T lymphocytes of the patient with aGVHD have higher MFI values of TLR-5 and lower MFI values of TLR-1 and -9 compared with the patient without aGVHD (A). An analogous TLR profile is displayed by monocytes (B).
Lateral Decubitus Anchors, supplied by Arthrex Inc, 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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Image Search Results


Impact of adropin on superoxide dismutase expression in pancreatic β‐cells of normoglycemic and diabetic rats. (A) Immunofluorescence labeling with anti‐superoxide dismutase antibody and anti‐insulin antibodies showed expression of superoxide dismutase in pancreatic β‐cells. (B) Quantification of the histological analysis showed a significant (*** p < 0.001) decrease in superoxide dismutase distribution in pancreatic endocrine cells and a significant (**** p < 0.0001) decrease in its localization in β‐cells of rats with diabetes when compared to the normal group. n = 6. Scale bar: 50 μm. Data analysis was done using the ANOVA test.

Journal: Animal Models and Experimental Medicine

Article Title: Adropin modulates pancreatic cell proliferation and glutathione levels in an animal model of type 1 diabetes mellitus

doi: 10.1002/ame2.70092

Figure Lengend Snippet: Impact of adropin on superoxide dismutase expression in pancreatic β‐cells of normoglycemic and diabetic rats. (A) Immunofluorescence labeling with anti‐superoxide dismutase antibody and anti‐insulin antibodies showed expression of superoxide dismutase in pancreatic β‐cells. (B) Quantification of the histological analysis showed a significant (*** p < 0.001) decrease in superoxide dismutase distribution in pancreatic endocrine cells and a significant (**** p < 0.0001) decrease in its localization in β‐cells of rats with diabetes when compared to the normal group. n = 6. Scale bar: 50 μm. Data analysis was done using the ANOVA test.

Article Snippet: Superoxide dismutase (rabbit) (1:500) , Rockland Immunochemicals, USA.

Techniques: Expressing, Immunofluorescence, Labeling

Effect of adropin on superoxide dismutase expression in pancreatic α‐cells of normal and diabetic rats. (A) Immunofluorescence staining using anti‐superoxide dismutase and anti‐glucagon antibodies showed expression of superoxide dismutase in pancreatic α‐cells. (B) Quantification of the histological analysis showed a significant (** p < 0.01) decrease in superoxide dismutase distribution in the pancreatic endocrine cells of diabetic rats compared to the normal group. α‐Cell expression of superoxide dismutase did not change with adropin treatment among all groups. n = 6. Scale bar: 50 μm. Data analysis was done using the ANOVA test.

Journal: Animal Models and Experimental Medicine

Article Title: Adropin modulates pancreatic cell proliferation and glutathione levels in an animal model of type 1 diabetes mellitus

doi: 10.1002/ame2.70092

Figure Lengend Snippet: Effect of adropin on superoxide dismutase expression in pancreatic α‐cells of normal and diabetic rats. (A) Immunofluorescence staining using anti‐superoxide dismutase and anti‐glucagon antibodies showed expression of superoxide dismutase in pancreatic α‐cells. (B) Quantification of the histological analysis showed a significant (** p < 0.01) decrease in superoxide dismutase distribution in the pancreatic endocrine cells of diabetic rats compared to the normal group. α‐Cell expression of superoxide dismutase did not change with adropin treatment among all groups. n = 6. Scale bar: 50 μm. Data analysis was done using the ANOVA test.

Article Snippet: Superoxide dismutase (rabbit) (1:500) , Rockland Immunochemicals, USA.

Techniques: Expressing, Immunofluorescence, Staining

Effect of adropin on catalase, superoxide dismutase and total glutathione activities in the serum samples of healthy and diabetic rats. (A) Catalase activity was significantly decreased in diabetic rats compared to normal controls. Adropin slightly increased catalase in DMT group. (B) Superoxide dismutase was slightly increased in DMT compared to the diabetic treated with adropin. (C) Total glutathione was significantly raised with adropin treatment in DMT compared to DMUT. n = 4–6. Data analysis was done using the ANOVA test. * p < 0.05.

Journal: Animal Models and Experimental Medicine

Article Title: Adropin modulates pancreatic cell proliferation and glutathione levels in an animal model of type 1 diabetes mellitus

doi: 10.1002/ame2.70092

Figure Lengend Snippet: Effect of adropin on catalase, superoxide dismutase and total glutathione activities in the serum samples of healthy and diabetic rats. (A) Catalase activity was significantly decreased in diabetic rats compared to normal controls. Adropin slightly increased catalase in DMT group. (B) Superoxide dismutase was slightly increased in DMT compared to the diabetic treated with adropin. (C) Total glutathione was significantly raised with adropin treatment in DMT compared to DMUT. n = 4–6. Data analysis was done using the ANOVA test. * p < 0.05.

Article Snippet: Superoxide dismutase (rabbit) (1:500) , Rockland Immunochemicals, USA.

Techniques: Activity Assay

Commercially available rapid diagnostic tools for the detection of T-2/HT-2 in cereals.

Journal: Toxins

Article Title: T-2 and HT-2 Toxins: Toxicity, Occurrence and Analysis: A Review

doi: 10.3390/toxins15080481

Figure Lengend Snippet: Commercially available rapid diagnostic tools for the detection of T-2/HT-2 in cereals.

Article Snippet: Of those, there were only a few that meet the requirements: the ROSA T-2 and HT-2 Quantitative Test (Charm Sciences Inc., Lawrence, MA, USA), T-2(T-2 Toxin) Lateral Flow Assay Kit (Elabscience Inc.) and the T2/HT2-V AQUA, (Vicam LP).

Techniques: Diagnostic Assay, Extraction, Solvent, Incubation, Sample Prep, Lateral Flow Assay, Enzyme-linked Immunosorbent Assay, Stripping Membranes

Figure 3. Comparison of LFA outputs versus albuterol concentration (ppb) for selected urine simu- lants. Aggregated LFA readout values from all urine simulants (n = 9) (A), from concentrated urine simulant (B), high salt only urine simulant, (C) and dilute urine simulant (D).

Journal: Biosensors

Article Title: Rapid and Simple Buffer Exchange Using Cation-Exchange Chromatography to Improve Point-of-Care Detection of Pharmacological Agents.

doi: 10.3390/bios13060635

Figure Lengend Snippet: Figure 3. Comparison of LFA outputs versus albuterol concentration (ppb) for selected urine simu- lants. Aggregated LFA readout values from all urine simulants (n = 9) (A), from concentrated urine simulant (B), high salt only urine simulant, (C) and dilute urine simulant (D).

Article Snippet: LFAs to detect albuterol (salbutamol) were acquired from ELabScience (Houston, TX, USA).

Techniques: Comparison, Concentration Assay

Figure 4. Comparison of LFA readout from two human saliva samples. LFAs with no processing return the same positive result if the samples contain 20 ppb albuterol (A) and 0 ppb albuterol (B). In comparison, processing using the method in this paper results in a clear signal when 20 ppb of albuterol is added to the sample (C) compared to when no albuterol is added (D) using either visual inspection (left) or an optical reader (right).

Journal: Biosensors

Article Title: Rapid and Simple Buffer Exchange Using Cation-Exchange Chromatography to Improve Point-of-Care Detection of Pharmacological Agents.

doi: 10.3390/bios13060635

Figure Lengend Snippet: Figure 4. Comparison of LFA readout from two human saliva samples. LFAs with no processing return the same positive result if the samples contain 20 ppb albuterol (A) and 0 ppb albuterol (B). In comparison, processing using the method in this paper results in a clear signal when 20 ppb of albuterol is added to the sample (C) compared to when no albuterol is added (D) using either visual inspection (left) or an optical reader (right).

Article Snippet: LFAs to detect albuterol (salbutamol) were acquired from ELabScience (Houston, TX, USA).

Techniques: Comparison

Figure 1. Expression of TLR-1, -5, and -9 on T lymphocytes and monocytes. Histogram plots of TLR-1, -5, and -9 expression in a patient with aGVHD and in a patient without aGVHD. The expression of surface (TLR-1 and -5) and intracellular (TLR-9) TLRs is reported with the corresponding negative control (mouse IgG1-PE). MFI is shown for each histogram. T lymphocytes of the patient with aGVHD have higher MFI values of TLR-5 and lower MFI values of TLR-1 and -9 compared with the patient without aGVHD (A). An analogous TLR profile is displayed by monocytes (B).

Journal: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

Article Title: Profile of toll-like receptors on peripheral blood cells in relation to acute graft-versus-host disease after allogeneic stem cell transplantation.

doi: 10.1016/j.bbmt.2012.09.013

Figure Lengend Snippet: Figure 1. Expression of TLR-1, -5, and -9 on T lymphocytes and monocytes. Histogram plots of TLR-1, -5, and -9 expression in a patient with aGVHD and in a patient without aGVHD. The expression of surface (TLR-1 and -5) and intracellular (TLR-9) TLRs is reported with the corresponding negative control (mouse IgG1-PE). MFI is shown for each histogram. T lymphocytes of the patient with aGVHD have higher MFI values of TLR-5 and lower MFI values of TLR-1 and -9 compared with the patient without aGVHD (A). An analogous TLR profile is displayed by monocytes (B).

Article Snippet: Intracellular staining for TLR-3, -7, -8, and -9 was performed using an Imgenex Intracellular Staining Flow Assay Kit according to the manufacturer’s instructions.

Techniques: Expressing, Negative Control