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| Product Name | Sorbitol Dehydrogenase (SDH) Activity Assay Kit, 100T/96S |
| Catalog No. | SCAK-YJL-0013 |
| Detection Method | Micro-volume method, Spectrophotometer/Microplate Reader |
| Storage | Store at -20°C, 6 months |
| Intended Use | For research use only. |
| Note | For your safety and health, please wear lab coat, disposable gloves and mask during operation. |
Sorbitol Dehydrogenase (SDH), with the enzyme classification number EC 1.1.1.14, is a key metabolic enzyme that catalyzes the reversible interconversion between sorbitol and fructose. In this enzymatic reaction, SDH facilitates the dehydrogenation of sorbitol to generate fructose, while simultaneously reducing nicotinamide adenine dinucleotide (NAD⁺) to its reduced form (NADH). This reaction is not only a critical step in regulating intracellular sorbitol levels but also plays a vital role in multiple physiological and pathological processes.
In the context of human health research, SDH activity is closely linked to two major areas: liver function and glucose metabolism-related disorders. Elevated levels of SDH in serum or plasma samples are widely recognized as a specific biomarker for liver damage, as the enzyme is predominantly expressed in liver cells. When liver tissue is injured (e.g., due to toxin exposure, inflammation, or structural damage), SDH is released into the bloodstream, making its activity a reliable indicator for researching liver disease mechanisms—especially when combined with other liver function markers like aminotransferases.
Additionally, SDH is a core enzyme in the polyol pathway, a key alternative pathway for glucose metabolism. Under normal physiological conditions, the polyol pathway is minimally active; however, in states of chronic hyperglycemia (such as in diabetes research models), glucose is converted to sorbitol via aldose reductase, and SDH then catalyzes the conversion of sorbitol to fructose. The accumulation of sorbitol and fructose in tissues (e.g., retinal cells, nerve cells) is closely associated with the development of diabetic complications, including proliferative diabetic retinopathy and diabetic neuropathy. Thus, measuring SDH activity is essential for studying the pathogenesis of these complications and evaluating potential therapeutic interventions.
Beyond human health research, SDH also has significant applications in plant biology studies. In plants, SDH participates in sugar metabolism and stress response mechanisms. For example, under abiotic stress conditions (e.g., drought, salinity, low temperatures), plants adjust their intracellular sugar composition to maintain osmotic balance and protect cellular structures—SDH activity directly influences the conversion between sorbitol and fructose, making it a key target for researching plant stress adaptation.
The Sorbitol Dehydrogenase (SDH) Activity Assay Kit is designed to quantitatively measure SDH activity in various biological samples, providing researchers with a reliable tool to explore the aforementioned physiological and pathological processes. By detecting changes in absorbance (a signal derived from NADH or its coupled reactions) using spectrophotometers or microplate readers, the kit enables accurate quantification of SDH activity, supporting research in fields such as hepatology, diabetes, and plant physiology.
Versatile Detection Compatibility: The kit is compatible with both spectrophotometers and microplate readers, supporting flexible sample analysis workflows—whether for small-batch sample testing (using spectrophotometers) or high-throughput screening (using microplate readers), meeting the diverse needs of different research scenarios.
Reliable Storage Stability: All components of the kit can be stored at -20°C for up to 6 months, ensuring long-term usability and consistent performance. This stability reduces the need for frequent reagent replacement, lowering research costs and operational complexity.
Broad Sample Applicability: The kit is suitable for analyzing SDH activity in a wide range of biological samples commonly used in research, including plasma, serum, urine, tissue homogenates, and cell culture media—eliminating the need for researchers to purchase multiple kits for different sample types.
Simple Experimental Protocol: The assay follows a straightforward "mix-incubate-measure" workflow, requiring no complex pre-treatment steps. This simplifies experimental operations, shortens the time required for each assay, and reduces the risk of human error, making it accessible to both experienced researchers and laboratory novices.
High Sensitivity for Accurate Detection: The kit’s detection method (based on monitoring absorbance changes associated with NADH production or coupled reactions) enables precise measurement of low SDH activity levels. This ensures that even subtle changes in SDH activity—critical for studying early-stage biological processes (e.g., initial liver damage or early diabetic complications)—are not missed.
Linear Detection Range for Flexible Quantification: The kit offers a linear detection range that covers a wide spectrum of SDH activity levels (e.g., 0.1 to 125 U/L for 20 μL samples when using standard protocols). This flexibility allows researchers to quantify both low and high SDH activity samples without the need for repeated dilution or concentration, improving experimental efficiency.
Non-Radioactive Assay Design: The kit uses a colorimetric or micro-volume detection principle (no radioactive reagents), ensuring safe experimental operations. This eliminates the risks associated with radioactive material handling (e.g., radiation exposure, waste disposal hazards) and complies with common laboratory safety regulations.
Consistent and Reproducible Results: The kit’s pre-formulated reagents and standardized protocol minimize batch-to-batch variations in assay performance. This ensures that experimental results are highly reproducible across different tests and laboratories, enhancing the reliability of research data for publication or further analysis.
For research use only, not for clinical use.
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