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Ta 2513

Manufactured by Biodiagnostic
Sourced in Egypt

The TA 2513 is a laboratory instrument designed for the analysis of biological samples. It features high-precision measurement capabilities and advanced data processing functionalities. The core function of the TA 2513 is to perform analytical tests and provide accurate results to support scientific research and medical diagnostics.

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5 protocols using ta 2513

1

Antioxidant and Inflammatory Markers in Colonic Tissue

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Catalase (Cat. No. CA2517), and total antioxidant capacity (TAC, Cat. No. TA 2513) were assessed spectrophotometrically in colonic tissue homogenate using commercial kits supplied by Bio-diagnostic (Giza, Egypt). Myeloperoxidase (MPO) activity (Cat. No. MAK068-1 KT) was assessed using a kit supplied by Sigma-Aldrich (MO, United States), where MPO catalyzes the formation of hypochlorous acid, which reacts with taurine to form taurine chloroamine. A colorless product, DTNB, is formed when taurine chloroamine reacts with the chromophore.
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2

Serum Antioxidant Capacity and Lipid Peroxidation Assay

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Total antioxidant capacity (TAC) in serum was determined by colorimetric method using a trade available kit (Cat. no# TA 2513) obtained from Bio-Diagnostics Company, Egypt, following previously outlined procedures (Koracevic et al., 2001 (link)). The anti-oxidative capacity in rat serum is measured by the reaction of antioxidants in the sample with a known amount of exogenously supplied hydrogen peroxide (H2O2), resulting in removing a specific amount of H2O2. The remaining H2O2 is estimated colorimetrically by an enzymatic reaction, which involves the conversion of 3, 5, dichloro–2–hydroxyl benzensulphonate to a colored product. The level of serum malondialdehyde (MDA), a major lipid peroxidation product, is measured colorimetrically using a commercially available kit (Cat. no# MD2529) obtained from Bio-Diagnostics Company, Egypt, following previously outlined instructions (Ohkawa et al., 1979 (link)). This assay is based on the reaction of thiobarbituric acid (TBA) with MDA in an acidic medium at a temperature of 95°C for 30 min to form a thiobarbituric acid reactive product with a pink color, with its absorbance measured at 534 nm. Serum TAC is measured in mM/L, while serum MDA is measured in nmol/ml.
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3

Antioxidant and Oxidative Stress Analysis

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The lung tissues were homogenized in 1–2 ml of 5 mM cold potassium phosphate buffer (pH 7.4), centrifuged at 4000 rpm for 15 min at 4 °C and the supernatant was removed and stored at − 80 °C for assay of total antioxidant capacity (TAC) (Cat. No. TA 25 13, Biodiagnostics) and malondialdehyde (MDA) (Cat. No. MD 25 29, Biodiagnostics).
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4

Evaluation of Hepatic Biochemical Profiles

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Isolated sera were used for the assessment of serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST) (cat. no. AT-1034; Bio-diagnostic), albumin (cat. no. AB-1010; Bio-diagnostic), bilirubin (cat. no. BR-1110; Bio-diagnostic), lactate dehydrogenase activity (LDH; cat. no. 278001; Spectrum Diagnostics), total cholesterol (cat. no. CH-1220; Bio-diagnostic) and triglycerides (TG; cat. no. TR-2030; Bio-diagnostic). Liver homogenates were used for estimating levels of lipid peroxides (measured as malondialdehyde, MDA; cat. no. MD-2529; Bio-diagnostic), catalase activity (cat. no. CA-2517, Bio-diagnostic) and total anti-oxidant activity (cat. no. TA-2513, Bio-diagnostic). Commercially available kits were used for measuring the different biochemical parameters according to the manufacturers' protocols.
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5

Measurement of Serum Testosterone, Antioxidant Capacity, and Lipid Peroxidation

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Serum testosterone concentrations were estimated according to Sato et al. [23 (link)] using the radioimmunoassay method. Serum samples were assayed for TAC using commercial kits according to the method described by Koracevic et al. [22 (link)] and for MDA levels according to Ohkawa et al. [24 (link)]. To do that, particular colorimetric test kits were utilized, following the manufacturer’s instructions (Biodiagnostic Company, Egypt; catalog numbers: MD 25 29 and TA 25 13 for MDA and TAC, respectively). MDA test based on thiobarbituric acid (TBA) reaction in an acidic solution at 95 °C for 30 min. A reactive product of thiobarbituric acid was formed as a result of this reaction. At 534 nm, the absorbance of the resultant colored substance was measured. Concerning TAC, the sample’s antioxidant content is reacted with a predetermined volume of exogenously supplied hydrogen peroxide (H2O2) to measure TAC. A portion of the H2O2 was removed from the sample by the antioxidants; the remaining H2O2 was then colorimetrically detected at 505 nm using an enzymatic process that produced a colored material from 3, 5, dichloro-2-hydroxybenzensulphonate.
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