LDH Assay Kit (Cytotoxicity, Fluorometric) (ab197004) provides a sensitive, quick, and easy way to detect LDH (lactate dehydrogenase) released from damaged cells.
Individual kit components also available for purchase with a minimum order of 20 units. Contact us to discuss your needs.
Fluorescent
Suspension cells, Adherent cells
Enzyme activity (quantitative)
Mammals
20m
= 100 Cells/well
L-lactate dehydrogenase A chain, LDH-A, Cell proliferation-inducing gene 19 protein, LDH muscle subunit, Renal carcinoma antigen NY-REN-59, LDH-M, PIG19, LDHA
LDH Assay Kit (Cytotoxicity, Fluorometric) (ab197004) provides a sensitive, quick, and easy way to detect LDH (lactate dehydrogenase) released from damaged cells.
Individual kit components also available for purchase with a minimum order of 20 units. Contact us to discuss your needs.
L-lactate dehydrogenase A chain, LDH-A, Cell proliferation-inducing gene 19 protein, LDH muscle subunit, Renal carcinoma antigen NY-REN-59, LDH-M, PIG19, LDHA
Fluorescent
Suspension cells, Adherent cells
Enzyme activity (quantitative)
Mammals
20m
Microplate reader
= 100 Cells/well
Blue Ice
-20°C
-20°C
-20°C
LDH Assay Kit (Cytotoxicity, Fluorometric) (ab197004) provides a sensitive, quick, and easy way to detect LDH (lactate dehydrogenase) released from damaged cells.
In the LDH assay, LDH converts lactate to pyruvate and NADH, which reduces a proprietary probe to an intensely fluorescent product (Ex/Em = 535/587 nm).
The amount of fluorescence is directly proportional to the number of damaged cells.
The assay is adaptable to high-throughput format and can be completed in less than 20 min. Sensitivity: ~ 100 cells. 5μl of cell culture media required per assay.
**Alternative LDH assays** If you would like to use a fluorometric assay, please refer to . This kit is more sensitive than the . To measure LDH activity in sample types such as serum, plasma, and cell lysates, we recommend . **Related products and guides to cytotoxicity / cell viability / proliferation assays** Review our to learn about our other kits to perform a , or .
This supplementary information is collated from multiple sources and compiled automatically.
Lactate dehydrogenase (LDH) is an enzyme that catalyzes the interconversion of pyruvate and lactate along with the conversion of NADH to NAD+. LDH is known by other names such as lactic acid dehydrogenase and LDH-5. The enzyme has a molecular weight of approximately 36 kDa. LDH exists in almost all tissues having multiple isoforms that are expressed differently depending on the tissue type. It shows high expression in muscle tissue liver and heart indicating its extensive role in energy metabolism.
Lactate dehydrogenase plays a critical role in anaerobic glycolysis. The enzyme helps in regenerating NAD+ from NADH allowing glycolysis to continue in the absence of oxygen. LDH is not a part of any larger protein complex working independently to fulfill its function in the glycolytic pathway. It serves in rapid energy production especially under hypoxic or exertional conditions where oxygen supply is limited.
LDH is significantly involved in the glycolysis and gluconeogenesis pathways. Within glycolysis LDH helps facilitate the conversion of pyruvate to lactate during anaerobic conditions a step important for ATP production when oxygen is scarce. The enzyme is tied closely to phosphofructokinase-1 (PFK-1) in glycolysis given that both enzymes are central to maintaining the glycolytic flow. In gluconeogenesis though functionally reversed from its role in glycolysis LDH helps to manage lactate removal an important step for glucose synthesis from non-carbohydrate sources.
Lactate dehydrogenase levels often act as a biomarker for tissue damage or certain cancers as its release into the bloodstream signals cellular injury or death. Elevated LDH levels are associated with conditions like myocardial infarction and certain forms of anemia. In cancer such as lymphoma or leukemia LDH correlates with the progression of the disease and acts as a prognostic marker. LDH's connection to these conditions often leads to insights into disease severity and progression due to its association with proteins like p53 and HIF-1 which play roles in cellular metabolism and hypoxia response.
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Untreated Jurkat cells or treated with Cell Lysis Solution.
Untreated Jurkat cells (low control) or treated with Cell Lysis Solution for 30 min (high control).
Relative Fluorescence Units of untreated Jurkat cells or treated with Cell Lysis Solution.
Relative fluorescence units of untreated Jurkat cells (low control) or treated with Cell Lysis Solution for 30 min (high control).
Overnight treatment of HeLa cells with staurosporine or cycloheximide.
Overnight treatment of HeLa cells with 100μM of staurosporine or 3μM of cycloheximide. LDH released into the medium was measured along with blank, untreated cells (low control), LDH Positive Control, and lysed cells (high control)
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