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CLIA Kit for Ischemia Modified Albumin (IMA) - UCCA825Hu

CLIA Kit for Ischemia Modified Albumin (IMA) - UCCA825Hu

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CLIA Kit for Ischemia Modified Albumin (IMA)

Size: 96T

Catalogue Number: UCCA825Hu-96

Citations, Manuals and MSDS Available upon request.

Target: Ischemia Modified Albumin (IMA)

Target Species: Human

Detection range: 370.4-30,000ng/mL

Sensitivity: 131.3ng/mL

Uniprot: P02768

Gene ID: 213

Featured Series Function: Detects small molecule

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

Assay Time: 2h

Method: Chemiluminescence

Specificity: Reactive with Human IMA / Ischemia Modified Albumin

Detection principle: Competitive Inhibition

Sample Size: 50uL

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

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 Ischemia Modified Albumin (IMA).
No significant cross-reactivity or interference between Ischemia Modified Albumin (IMA) and analogues was observed.

Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Ischemia Modified Albumin (IMA) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Ischemia Modified Albumin (IMA) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100

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 100µL Substrate Solution. Incubate 10 minutes at 37°C;
7. Read RLU value immediately.

Test principle: The microplate provided in this kit has been pre-coated with a monoclonal antibody specific to Ischemia Modified Albumin (IMA). A competitive inhibition reaction is launched between biotin labeled Ischemia Modified Albumin (IMA) and unlabeled Ischemia Modified Albumin (IMA) (Standards or samples) with the pre-coated antibody specific to Ischemia Modified Albumin (IMA). 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 Ischemia Modified Albumin (IMA) in the sample. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is reverse proportional to the Ischemia Modified Albumin (IMA) level in the sample or standard.

Research Area: Metabolic pathway; Cardiovascular biology;

Research Use Only