CLIA Kit for Interleukin 8 (IL8) View larger

CLIA Kit for Interleukin 8 (IL8)

CC-SCA080Po

New product

48T, 96T, 96T×5, 96T×10, 96T×100

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Data sheet

Size 48T, <i>96T</i>, 96T×5, 96T×10, 96T×100
Storage Conditions -20°C
Shipping Conditions Entre 4°C y 8°C
Applications Chemiluminescent immunoassay for Antigen Detection.
Detection Range 27.4-20,000pg/mL
Sensitivity The minimum detectable dose of this kit is typically less than 12.8pg/mL
Research Area Cytokine
Organism species Sus scrofa
Alternative Names CXCL8
Item Name Interleukin 8
Assay Length 2h, 40min
Method Double-antibody Sandwich
Sample Type Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Formato 48T, <i>96T</i>, 96T×5, 96T×10, 96T×100
Test Principle The microplate provided in this kit has been pre-coated with an antibody specific to Interleukin 8 (IL8). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Interleukin 8 (IL8). Next, Avid
Assay procedure summary 1. Prepare all reagents, samples and standards
UniProt ID P26894

More info

Especificidad:

This assay has high sensitivity and excellent specificity for detection of Interleukin 8 (IL8).
No significant cross-reactivity or interference between Interleukin 8 (IL8) and analogues was observed.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Interleukin 8 (IL8) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Interleukin 8 (IL8) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Estabilidad:

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.

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