Quantikine
Duoset
Luminex
Array
MISC
100

Validated sample types for Qkits


What is - Serum, plasma, cell culture supernates (not all kits, milk, urine, saliva, tissue lysates, and tissue homogenates)

100

Components within Duoset kit

What is~ Capture, Detection, Standard, and Streptavidin HRP

100
Number of Analytes able to be plexed together

What is~ up to 50

100

Number of Membranes within an Array kit

What is ~ 4 membranes per kit (some have 8) 

100

Kits that can be run as a partial plate

What are~ Quantikine and Duoset ~ Quantikine comes with removable strips, Duosets depend on the plates they purchase, but can be run partially. Luminex has black plates that can be covered for partial runs.  

200

Number of samples for Qkits


What is ~ 40 

Most Quantikine ELISA Kits will run the standard curve and 40 samples in duplicate.

200

Validated sample types for Duoset

What is ~ Only cell culture supernates, Duoset IC - cell culture lysates. Can be optimized for plasma and serum. 
200

Definition of Multiplexing

What is ~ multiplexing allows multiple biological target analytes to be simultaneously examined and quantified in a single sample. It’s a technique widely used by scientific researchers of all disciplines and provides many benefits.


200

Validated sample types for Array kit

What is ~ Serum, plasma, tissue lysate, cell lysates, (some breast milk, urine, saliva, tissue homogenates, etc)

200

Explain the mechanism of sandwich ELISA

What is ~ A sandwich ELISA uses an immobilized capture antibody specific for the analyte of interest in a sample. After the analyte is bound to the immobilized antibody, a labeled secondary antibody specific for the analyte is used for detection. The analyte is "sandwiched" between the two antibodies

300

What is the master calibrator?

What is~ Test against our master calibrator for consistent immunoreactivity.


300

Importance of Wavelength Correction

What is~ This subtraction will correct for optical imperfections or refraction created by the plastic plate


300

Describe split based dilution

What is~ This keeps analytes requiring the same dilution factor within a single panel, while separating analytes requiring different dilutions.

300

Number of samples used to analyze in Array kit

What is ~ 4 samples per kit 

300

Explain the mechanism of Competitive ELISA

What is ~ In the competitive immunoassay approach, also termed "labeled analyte technique", there exists a competition between the endogenous unlabeled antigen and an exogenous labeled antigen for a limited amount of antibody binding sites. Therefore, a decreasing signal indicates higher concentrations of the analyte being measured.

400

Expiration for Qkits

What is~ dependent on the component with the shortest shelf life. But a minimum of 12 weeks (shipdown date) 

400

Controls for Duoset kit

What is~ QC control sets are not available for DuoSet ELISAs as they are developmental assays with only core reagents- End-user will need to find their own

400

Software used to analyze Luminex results

What is ~ Quantist (xPonent can also analyze)

400

Normalization uses within an Array kit

What is ~ You cannot normalize an Array kit as it is a Qualitative assay. 

Array kits are designed to compare relative expression levels of analytes in treated and non-treated samples.  Reference spots consist of an unrelated biotinylated protein spotted directly to the membranes.  

Signal from these reference spots indicates that the kit detection system is working and also provides guidance spots for aligning the membrane to the template

400

Elispot uses/application purpose

What is~ used for detection of cytokine-secreting cells


500

Customer received Qkit and needs more wash buffer

What is ~ Wash buffer can be purchased separately. 

Wash Buffer Concentrate, 25X Catalog #: WA126

500

Difference between Quantikine and Duoset kit

What is~ Duoset kit only has 4 components and will need ancillary materials purchased by end-user. User coats plate

Quantikine kit has most of the necessary materials to run kit. Pre-coated plates. 

500

Difference between discovery and high performance kit

What is~ A High Performance Assay consists of select analytes which have been thoroughly tested and validated together as a panel. The diluents provided in the High Performance kits and assay conditions have been optimized for best results with the analytes on the same panel. The High Performance Assay is the most precise, reproducible and accurate Luminex tool offered by R&D Systems and are correlated to our gold standard Quantikine ELISA kits. Controls are available for the Human Luminex High Performance Assays. The Luminex Discovery Assay option is a flexible tool, providing the uncommon opportunity to customize by mixing and matching analytes across different panels. Although not as extensively tested as the High Performance Assays, analytes on a Luminex Assay are tested together when built and a final quality control test on each Luminex Assay is performed prior to release. Since each Luminex Assay is unique and built to order, additional days are required for order fulfillment and it is not characterized by the same level of optimization and validation testing as with the High Performance assays. Controls are not available for Luminex Assay. In general, the sensitives of the Luminex Discovery Assays and Luminex High Performance Assays are similar. For low abundance cytokines, High Sensitivity panels are available for High Performance Assay, which are not available for Luminex Assay. 

500

Detection system used for Array kits

What are~ film, camera, (Some kits have been validated for Li-Cor)


500

Define Matrix Effect

What is~ 

  • A matrix effect describes an inaccurate result due to a substance that interferes with the assay. Interference can be specific due to soluble receptors or other binding proteins competing for the antigen; interference can be semi-specific due to factors or substances such as heterophilic antibodies, autoantibodies, complement, and rheumatoid factors that interfere with the antibody binding causing false positive or negative results. Non-specific interference is due to protein concentration, ionic strength, pH, and other serum components that can affect the equilibrium or kinetics of binding between antigen and antibodies.