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SKU:SCB883Hu

CLIA Kit for Apolipoprotein B48 (APOB48)

CLIA Kit for Apolipoprotein B48 (APOB48)

Regular price $840.00 USD
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UOM
Sensitivity
Detection range

Chemiluminescent immunoassay for Antigen Detection.

Product No.

SCB883Hu

Organism Species

Homo sapiens (Human).

Sample Type

Serum, plasma and other biological fluids.

Test Method

Double-antibody Sandwich

Assay Length

2h, 40min

Detection Range

0.69-500pg/mL

Sensitivity

The minimum detectable dose of this kit is typically less than 0.28pg/mL.

UOM

48T 96T 96T*5 96T*10 96T*100

Specificity

This assay has high sensitivity and excellent specificity for detection of Apolipoprotein B48 (APOB48).
No significant cross-reactivity or interference between Apolipoprotein B48 (APOB48) and analogues was observed.

Recovery

Matrices listed below were spiked with certain level of recombinant Apolipoprotein B48 (APOB48) and the recovery rates were calculated by comparing the measured value to the expected amount of Apolipoprotein B48 (APOB48) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 93-102 96
EDTA plasma(n=5) 91-99 95
heparin plasma(n=5) 81-91 86

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Apolipoprotein B48 (APOB48) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Apolipoprotein B48 (APOB48) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Apolipoprotein B48 (APOB48) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample 1:2 1:4 1:8 1:16
serum(n=5) 90-104% 78-91% 84-98% 86-99%
EDTA plasma(n=5) 78-103% 98-105% 86-102% 81-104%
heparin plasma(n=5) 98-105% 80-89% 82-104% 79-104%

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.

Reagents and materials provided

Reagents Quantity Reagents Quantity
Pre-coated, ready to use 96-well strip plate 1 Plate sealer for 96 wells 4
Standard 2 Standard Diluent 1×20mL
Detection Reagent A 1×120µL Assay Diluent A 1×12mL
Detection Reagent B 1×120µL Assay Diluent B 1×12mL
Substrate A 1×10mL Substrate B 1×2mL
Wash Buffer (30 × concentrate) 1×20mL Instruction manual 1

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

Magazine Citations
Steroids Effects of Anabolic Androgenic Steroids on Chylomicron Metabolism PubMed: 22939845
Human Health and Nutritional Sciences The Influences of Pectin and Apples, as a Pectin-rich Food Matrix, on Lipid Digestibility, Bioaccessibility and Postprandial Lipemia
British Journal of Nutrition Acute whole apple consumption did not influence postprandial lipemia: A randomized crossover trial Pubmed: 31902373
Clinical Nutrition Postprandial dyslipidemia after a standardized high-fat meal in BMI-matched healthy individuals, and in subjects with prediabetes or Type 2 diabetes 34656950
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