MDA Hign-sensitive ELISA kit (General species)

SKU: HEA597Ge

Size: 96Tests

# of Times Cited in literature: 1

Prepare Time: 1-3 days(please inquire for mutiple units)

Target Name: MDA

Target Full Name: Malondialdehyde

Alternative Names: -

Target Species: General species

Uniprot: -

Gene ID: -

Featured Series: HE kit

Featured Series Function: Detects protein (low-target protein, high-sensitivity)

Specificity: Reactive with General species MDA / Malondialdehyde

Method: Colormetric

Detection principle: Competitive Inhibition

Detection range: 12.35-1,000ng/mL

Sensitivity: 4.94ng/mL

Assay Time: 3h

Sample Size: 50uL

Recommended/Predicted Sample Types: Serum, Plasma and other Biological Fluids

Assay Precision: Intra-Assay: CV<10%, Inter-Assay: CV<12%

Reproducibility test menthod: 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

Storage: 4°C for 1 month/ -20°C for long-term(One year within shelf life)

Shelf-life: 12 months

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.

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 50µL standard or sample to each well. And then add 50µL prepared Detection Reagent A immediately. Shake and mix. Incubate 1 hour at 37°C; 3. Aspirate and wash 3 times; 4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C; 5. Aspirate and wash 5 times; 6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C; 7. Add 50µL 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;

References Citing This Product: The Influence of Probiotic Supplementation on Depressive Symptoms, Inflammation and Oxidative Stress Parameters and Faecal Microbiota in Patients with Depression Depending on Metabolic Syndrome Comorbidity ¨C PRO-DEMET Randomised Study Protocol