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E-mail
3004965510@qq.com
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Phone
15000017673
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Address
Shanghai Songjiang District, Shanghai
Shanghai Bangjing Industrial Co., Ltd
3004965510@qq.com
15000017673
Shanghai Songjiang District, Shanghai
Product attributes:
Product Name:Glucose oxidase test kit50 tubes/24 samples
Detection method: Visible spectrophotometry
Product Category: Oxidation and Antioxidant Series
Product Specifications50 tubes/24 samples
Detection method: Visible spectrophotometry
Product Code:BJ-01S9607
Product Introduction:
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Measurement significance: GOD (EC 1.1.3.4) is widely present in animals and plants, catalyzing the oxidation of glucose to produce gluconic acid and H2O2, and is one of the metabolic pathways for the production of reactive oxygen species in organisms. Measurement principle: GOD catalyzes the production of H2O2, and peroxidase catalyzes the decomposition of H2O2 in the presence of oxygen, producing oxygen that oxidizes ortho anisidine to produce colored substances. The color intensity is linearly related to the activity of glucose oxidase. Instruments and equipment required for the experiment: Visible spectrophotometer/ELISA reader, water bath, desktop centrifuge, adjustable pipette, 1 mL glass colorimetric dish/96 well plate, mortar, ice, distilled water. |
Required instruments and supplies:
Visible spectrophotometer1mL glass colorimetric dish (optical path 1cm), low-temperature centrifuge, pipette, mortar, ice, and distilled water
4、 Superoxide Dismutase(Determination of SOD:
Suggest selecting before the formal experimentMake predictions for 2 samples, understand the situation of this batch of samples, familiarize yourself with the experimental process, and avoid experiments
Waste of samples and reagents!
1. Sample preparation
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①Organizational sample: Take an appointment0.1gOrganizations (samples with sufficient moisture can be taken)0.25g)Join in1mLExtract liquid, in4ºCOr take an ice bath homogenate(Or use various common homogenizers).4ºC×12000rpmcentrifugation10minTake the supernatant as the test solution. [Note]: If the sample size is increased, it can be based on the quality of the organization(g)Volume of extraction solution(mL)for1:5~10Extract the proportion
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②bacteria/Cell samples: Collect bacteria or cells into a centrifuge tube first, centrifuge and discard the supernatant; Take an appointment500 Ten thousand bacteria or cells added1mL Extraction solution, ultrasonic disruption of bacteria or cells (ice bath, power)200W, Ultrasound3sinterval10sRepeat, repeat30 Secondary); 12000rpm 4℃centrifugation10minTake the supernatant and place it on ice for testing. [Note]: If the sample size is increased, it can be classified according to bacteria/Number of cells(10) |
4) Extract in a ratio of 500-1000:1 using an extraction solution (mL). ③ Liquid sample: direct detection; If turbid, centrifuge and take the supernatant for detection.
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Notes:
1. Reagent 2 is an enzyme and cannot be frozen. It should be placed on ice during use.
2. Only one care is needed.
3. If the absorbance value of the control tube is greater than 2, it is recommended to dilute reagent 2 with distilled water by 7 times before use (10 μ l of reagent 2 original solution+60 μ l of distilled water).
4. Why are some sample measuring tubes larger than the control tube for SOD, and what is the range of values for the control tube?
The scope of care is0.8-2. The low absorbance value of the control tube may be due to (1) reagent two or reagent four not being prepared and used immediately; (2) Not adding reagents in order; (3) The reaction time is not sufficient, and can be extended (reaction time of 30 minutes can be extended to 40 minutes). The high absorbance value of the control tube may be due to reagent 2 not being diluted by the corresponding multiple according to the operating instructions.
If the measuring tube is larger than the control tube, it may be due to the significant influence of impurities in the sample. In order to reduce the impact of impurities, the sample extraction supernatant is usually diluted with distilled water or extraction solutionTesting 10 times later can usually make the measurement normal. Multiply by the corresponding dilution factor in the calculation formula.