ELISA Kit for Poly A Specific Ribonuclease (PARN) - USEC176Hu

ELISA Kit for Poly A Specific Ribonuclease (PARN)

Size: 96T

Catalogue Number: USEC176Hu-96

Citations, Manuals and MSDS Available upon request.

Target: Poly A Specific Ribonuclease (PARN)

Alternative Names: DAN; Deadenylation Nuclease; Deadenylating nuclease; Polyadenylate-specific ribonuclease

Target Species: Human

Detection range: 0.781-50ng/mL

Sensitivity: 0.27ng/mL

Uniprot: O95453

Gene ID: 5073

Featured Series Function: Detects protein (regular version)

Recommended/Predicted Sample Types: Tissue Homogenates and other Biological Fluids

Assay Time: 3h

Method: Colormetric

Specificity: Reactive with Human PARN / Poly A Specific Ribonuclease

Detection principle: Double-antibody Sandwich

Sample Size: 100uL

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 Poly A Specific Ribonuclease (PARN).

No significant cross-reactivity or interference between Poly A Specific Ribonuclease (PARN) and analogues was observed.

Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Poly A Specific Ribonuclease (PARN) were tested 20 times on one plate, respectively.

Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Poly A Specific Ribonuclease (PARN) 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 100µL standard or sample to each well. Incubate 1 hours at 37°C;

3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;

4. Aspirate and wash 3 times;

5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;

6. Aspirate and wash 5 times;

7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;

8. Add 50µL Stop Solution. Read at 450nm immediately.

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Poly A Specific Ribonuclease (PARN). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Poly A Specific Ribonuclease (PARN). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Poly A Specific Ribonuclease (PARN), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Poly A Specific Ribonuclease (PARN) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Research Area: Enzyme & Kinase;

Research Use Only