TBARS Assay Kit
€0.00
In stock
SKU
CA995
Catalog Number: CA995 (96 assays
Accurate, Simple & Fast Colorimetric or Fluorometric MDA Quantitation
Information
Datasheet
Accurate, Simple & Fast Colorimetric or Fluorometric MDA Quantitation
Information
Datasheet
Oxidative stress in the cellular environment results in the formation of highly reactive and unstable lipid hydroperoxides. Decomposition of the unstable peroxides derived from polyunsaturated fatty acids results in the formation of malondialdehyde (MDA), which can be quantified colorimetrically following its controlled reaction with thiobarbituric acid. Thiobarbituric Acid Reactive Substances (TBARS) assay was proposed over 40 years ago and is now the most commonly used of method to screening and monitoring lipid oxidation.
TBARS method has been used to evaluate a wide range of samples that include human and animal tissues and fluids, drugs, foods and natural products. The sensitivity of measuring Thiobarbituric Acid Reactive Substances (TBARS) has made this assay the method of choice for screening and monitoring lipid peroxidation, a major indicator of oxidative stress. Even though there remains a controversy cited in literature regarding the specificity of TBARS toward compounds other than MDA, it still remains the most widely employed assay used to determine lipid peroxidation.
This assay is based on the reaction of malondialdehyde (MDA) with thiobarbituric acid (TBA); TBA reacts with MDA to form a pink chromogen, which can be detected spectrophotometrically at 532 nm.
Advantages & Features
- Accurate.
- Simple & Fast Protocol.
- Versatile: Colorimetric or Fluorometric MDA Quantitation.
- Standardized tool for assaying lipid peroxidation in Plasma, Serum, Urine, Tissue homogenates, and Cell Lysates.
Includes
- 4 x 0.53 g Thiobarbituric Acid (TBA)
- 40 mL Diluent 1 (contain Acetic Acid)
- 20 mL Diluent 2 (contain NaOH)
- 10 mL SDS Solution
- 250 μL MDA Standard (10mM)
- 20 mL H2O2 solution
- 1 unit 96-Well Solid Black plate
- 1 unit 96-Well Solid Clear plate
- 2 Adhesive strips
Applications
- For quantitative determination of lipid Peroxides (thiobarbituric acid reactive substances, TBARS).
- Evaluation of drug effects on lipid Peroxidation.
Shipping & Storage
Shipment:: Gel Pack.
Storage: 4 °C upon receipt.
TBARS method has been used to evaluate a wide range of samples that include human and animal tissues and fluids, drugs, foods and natural products. The sensitivity of measuring Thiobarbituric Acid Reactive Substances (TBARS) has made this assay the method of choice for screening and monitoring lipid peroxidation, a major indicator of oxidative stress. Even though there remains a controversy cited in literature regarding the specificity of TBARS toward compounds other than MDA, it still remains the most widely employed assay used to determine lipid peroxidation.
This assay is based on the reaction of malondialdehyde (MDA) with thiobarbituric acid (TBA); TBA reacts with MDA to form a pink chromogen, which can be detected spectrophotometrically at 532 nm.
Advantages & Features
- Accurate.
- Simple & Fast Protocol.
- Versatile: Colorimetric or Fluorometric MDA Quantitation.
- Standardized tool for assaying lipid peroxidation in Plasma, Serum, Urine, Tissue homogenates, and Cell Lysates.
Includes
- 4 x 0.53 g Thiobarbituric Acid (TBA)
- 40 mL Diluent 1 (contain Acetic Acid)
- 20 mL Diluent 2 (contain NaOH)
- 10 mL SDS Solution
- 250 μL MDA Standard (10mM)
- 20 mL H2O2 solution
- 1 unit 96-Well Solid Black plate
- 1 unit 96-Well Solid Clear plate
- 2 Adhesive strips
Applications
- For quantitative determination of lipid Peroxides (thiobarbituric acid reactive substances, TBARS).
- Evaluation of drug effects on lipid Peroxidation.
Shipping & Storage
Shipment:: Gel Pack.
Storage: 4 °C upon receipt.
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