Item no. |
HEA597Ge-24T |
Manufacturer |
Cloud-Clone
|
Amount |
24T |
Category |
|
Type |
Elisa-Kit |
Specific against |
other |
ECLASS 10.1 |
32160605 |
ECLASS 11.0 |
32160605 |
UNSPSC |
41116126 |
Available |
|
Quantity options |
|
Detection range |
12.35-1, 000ng/mL |
Organism species |
Pan-species (General) |
Sensitivity |
The minimum detectable dose of this kit is typically less than 4.94ng/mL |
Sample type |
Serum, plasma and other biological fluids |
Assay length |
3h |
Method |
Competitive Inhibition |
Specificity |
This assay has high sensitivity and excellent specificity for detection of High Sensitive Malondialdehyde (MDA). No significant cross-reactivity or interference between High Sensitive Malondialdehyde (MDA) and analogues was observed. |
Precision |
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level High Sensitive Malondialdehyde (MDA) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level High Sensitive Malondialdehyde (MDA) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100 Intra-Assay: CV<10% Inter-Assay: CV<12% |
Stability |
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end. |
Assay procedure summary |
1. Prepare all reagents, samples and standards; 2. Add 50µ L standard or sample to each well. And then add 50µ L prepared Detection Reagent A immediately. Shake and mix. Incubate 1 hour at 37° C; 3. Aspirate and wash 3 times; 4. Add 100µ L prepared Detection Reagent B. Incubate 30 minutes at 37° C; 5. Aspirate and wash 5 times; 6. Add 90µ L Substrate Solution. Incubate 10-20 minutes at 37° C; 7. Add 50µ L Stop Solution. Read at 450 nm immediately. |
Test principle |
This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to High Sensitive Malondialdehyde (MDA) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled High Sensitive Malondialdehyde (MDA) and unlabeled High Sensitive Malondialdehyde (MDA) (Standards or samples) with the pre-coated antibody specific to High Sensitive Malondialdehyde (MDA). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of High Sensitive Malondialdehyde (MDA) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of High Sensitive Malondialdehyde (MDA) in the sample. |
Research Area |
Metabolic pathway; Hepatology; Hormone metabolism; |
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.