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Interaction effect of foliar application with BHS treatments (T1: 0, T2: 1.0, and T3: 1.5%) and various levels of salinity (S1: 0, S2: 100, S3: 150, and S4: 200 mM NaCl) on antioxidant enzymes and osmolytes of Triticum aestivum L., cv. Yecora Rojo plants. (A) SOD, superoxide dismutase, (B) POD, <t>peroxidase,</t> (C) CAT, catalase (Enzyme units), (D) GB, glycine betaine (µg g -1 FW), and (E) proline (µg g -1 FW).
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Interaction effect of foliar application with BHS treatments (T1: 0, T2: 1.0, and T3: 1.5%) and various levels of salinity (S1: 0, S2: 100, S3: 150, and S4: 200 mM NaCl) on antioxidant enzymes and osmolytes of Triticum aestivum L., cv. Yecora Rojo plants. (A) SOD, superoxide dismutase, (B) POD, <t>peroxidase,</t> (C) CAT, catalase (Enzyme units), (D) GB, glycine betaine (µg g -1 FW), and (E) proline (µg g -1 FW).
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Elabscience Biotechnology peroxidase pod activity assay kit
Figure 4. Antioxidative enzyme activity in the two genotypes. (A). Ascorbate <t>peroxidase</t> (APX) activity in LT and LS, in all three time points (24 h, 72 h, 7 d). APX activity is shown as APX units/mg of protein. (B). Peroxidase <t>(POD)</t> activity in LT and LS, in all three time points (24 h, 72 h, 7 d). POD activity is shown as POD units/mg of protein. Control samples are shown in orange, and treatment samples are shown in blue. The significance of the difference between the control and treatment of each parameter was determined by t-test and is shown as ** (p < 0.01), * (p < 0.05), and NS (statistically not significant at p > 0.05).
Peroxidase Pod Activity Assay Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
peroxidase pod activity assay kit - by Bioz Stars, 2026-07
94/100 stars
  Buy from Supplier

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Interaction effect of foliar application with BHS treatments (T1: 0, T2: 1.0, and T3: 1.5%) and various levels of salinity (S1: 0, S2: 100, S3: 150, and S4: 200 mM NaCl) on antioxidant enzymes and osmolytes of Triticum aestivum L., cv. Yecora Rojo plants. (A) SOD, superoxide dismutase, (B) POD, peroxidase, (C) CAT, catalase (Enzyme units), (D) GB, glycine betaine (µg g -1 FW), and (E) proline (µg g -1 FW).

Journal: Frontiers in Plant Science

Article Title: Exogenous biostimulant bee-honey solution improves Triticum aestivum L. tolerance to salt stress by modulating physio-biochemical responses and upregulation of salinity-related genes

doi: 10.3389/fpls.2025.1761667

Figure Lengend Snippet: Interaction effect of foliar application with BHS treatments (T1: 0, T2: 1.0, and T3: 1.5%) and various levels of salinity (S1: 0, S2: 100, S3: 150, and S4: 200 mM NaCl) on antioxidant enzymes and osmolytes of Triticum aestivum L., cv. Yecora Rojo plants. (A) SOD, superoxide dismutase, (B) POD, peroxidase, (C) CAT, catalase (Enzyme units), (D) GB, glycine betaine (µg g -1 FW), and (E) proline (µg g -1 FW).

Article Snippet: As for POD activity evaluation, the peroxidase activity analytical kit (product No. E-BC-K227-S, Elabscience, United States) was used based on the provided protocol.

Techniques:

Figure 4. Antioxidative enzyme activity in the two genotypes. (A). Ascorbate peroxidase (APX) activity in LT and LS, in all three time points (24 h, 72 h, 7 d). APX activity is shown as APX units/mg of protein. (B). Peroxidase (POD) activity in LT and LS, in all three time points (24 h, 72 h, 7 d). POD activity is shown as POD units/mg of protein. Control samples are shown in orange, and treatment samples are shown in blue. The significance of the difference between the control and treatment of each parameter was determined by t-test and is shown as ** (p < 0.01), * (p < 0.05), and NS (statistically not significant at p > 0.05).

Journal: Biology

Article Title: The Early Growth of Maize Under Waterlogging Stress, as Measured by Growth, Biochemical, and Molecular Characteristics.

doi: 10.3390/biology14020111

Figure Lengend Snippet: Figure 4. Antioxidative enzyme activity in the two genotypes. (A). Ascorbate peroxidase (APX) activity in LT and LS, in all three time points (24 h, 72 h, 7 d). APX activity is shown as APX units/mg of protein. (B). Peroxidase (POD) activity in LT and LS, in all three time points (24 h, 72 h, 7 d). POD activity is shown as POD units/mg of protein. Control samples are shown in orange, and treatment samples are shown in blue. The significance of the difference between the control and treatment of each parameter was determined by t-test and is shown as ** (p < 0.01), * (p < 0.05), and NS (statistically not significant at p > 0.05).

Article Snippet: In alignment with the manufacturer’s instructions, the peroxidase (POD) Activity Assay Kit (Elabscience®, Wuhan, China) was employed for this purpose.

Techniques: Activity Assay, Control