-
- 抗原
- Superoxide Dismutase
- 应用范围
- Activity Assay (AcA)
- 样品类型
- Blood, Cell Culture Supernatant, Cell Extracts
- 特异性
- 0.05 U/mL
- 产品特性
-
Sensitive and accurate. Linear detection range of 0.05 - 3 U/mL SOD.
Convenient and high-throughput.
Homogeneous mix-incubate-measure type assay. No wash and reagent transfer steps are involved. Can be readily automated on HTS liquid handling systems for processing thousands of samples per day. - 组件
- Assay Buffer: 20 mL. Diluent: 20 mL. SOD Enzyme: 120 µL. XO Enzyme: 120 µL. Xanthine: 600 µL. WST-1: 600 µL.
- 试剂未包括
- Pipetting devices, tissue homogenizer, centrifuge and tubes, clear flat- bottom 96-well plates and plate reader.
-
Superoxide Dismutase ELISA Kit
适用: 人 Colorimetric Sandwich ELISA 0.781 ng/mL - 50 ng/mL Plasma, Serum, Tissue Homogenate
-
- 应用备注
- Determination of SOD in blood, cell, tissue and other biological samples.
- 实验流程
-
Note: If not assayed immediately, samples can be stored at -80°C for one month. All samples can be diluted in 50 mM potassium phosphate, pH 7.4.
1. Tissue samples. Perfuse tissue with cold PBS to remove any red blood cells. Homogenize tissue at 5 mL/g in cold lysis buffer (50mM potassium phosphate, 0.1 mM EDTA, 0.5% Triton X-100). Centrifuge at 12,000g for 5 minutes at 4°C. Use supernatant for total SOD assay.
2. Cell samples. Suspension cells: Centrifuge 1-2 x 10 6 cells at 800g for 2 minutes and discard supernatant. Wash cells with cold PBS, centrifuge, and discard the supernatant. Resuspend cells in 0.5 mL of cold lysis Buffer. After 10 min on ice, centrifuge at 12,000g for 5 min. Use supernatant for total SOD assay. Adherent cells: Wash 1-2 x 10 6 cells cold PBS. Place dish on ice. Add 0.5 mL of cold lysis buffer. After 10 min on ice, collect cells/debris with a rubber policeman. Centrifuge the cell extract at 12,000g for 5 min. Use supernatant for total SOD assay. Note: if it is desired to determine cytosolic and mitochondrial SOD activities separately, tissue/cell samples can be prepared according to Mattiazzi et al (2002). JBC 277: 29626-33.
3. Blood samples: Collect serum, or plasma (heparin, citrate or EDTA) using standard protocols. The erythrocyte pellet can be lysed in 5x volume of cold dH2O, centrifuge at 12,000g for 5 min to pellet the erythrocyte membranes. Dilute serum/plasma 1:5, red cell lysate 1:100 prior to SOD assay. Prior to assay, bring all reagents to room temperature (25°C). The Xanthine reagent may appear to be turbid. Briefly vortext this tube before pipetting. Briefly centrifuge enzyme tubes, keep on ice during assay.
1. Standards. Mix 8µL SOD Enzyme with 392µL Diluent to give 3U/mL SOD standard. Dilute standards. Transfer 20 µL samples to separate wells.
2. Prepare enough Working Reagent for the standard and sample wells. For each well, mix 160 µL Assay Buffer, 5 µL Xanthine and 5 µL WST-1. Transfer 160 µL Working Reagent to each well and tap plate to mix. For each well, dilute the XO Enzyme 1:20 in Diluent. Quickly add 20 µL diluted XO enzyme to each assay well (use of a multi-channel pipettor is recommended). Tap plate to mix.
3. Immediately read OD440nm (OD420-460nm) (ODo). Incubate for 60 min at room temperature (25°C) in the dark. Read OD440nm again (OD60). - 结果分析
-
- For each standard and sample well, calculate OD60 = OD60 - ODo.
2. Calculate OD = ODstd8 - OD for each standard and sample where ODstd8 is the OD for Standard # 8 (the standard with no SOD activity and highest possible absorbance).
3. Plot the Standard Curve OD vs SOD. Use the OD for sample to determine SOD activity of sample from the standard curve.
- For each standard and sample well, calculate OD60 = OD60 - ODo.
- 限制
- 仅限研究用
-
- 储存条件
- -20 °C
-
- 抗原
- Superoxide Dismutase
- 别名
- GTP-binding nuclear protein Ran Kit, superoxide dismutase 1 Kit, LOC786258 Kit, SOD1 Kit
- 背景
-
Quantitative determination of superoxide dismutase (SOD) enzyme activity by colorimetric (440nm) method.
Procedure: 1 hr.
Superoxide Dismutases (SOD, EC1.15.1.1) are enzymes that catalyze the dismutation of superoxide into O2 and H2O2. They are an important antioxidant defense in all cells exposed to O2. There are three major families of superoxide dismutase: Cu/Zn, Fe/Mn, and the Ni type. Aberrant SOD activities have been linked to diseases such as amyotrophic lateral sclerosis, perinatal lethality, neural disorders and cancer. This SOD assay provides a convenient colorimetric means for the quantitative determination of SOD enzyme activity in biological samples. In the assay, superoxide (O2-) is provided by xanthine oxidase (XO) catalyzed reaction. O2- reacts with a WST-1 dye to form a colored product. SOD scavenges the O2- thus less O2- is available for the chromogenic reaction. The color intensity (OD440nm) is used to determine the SOD activity in a sample.
-
You are here:
