Vergleich

Multiplex Assay Kit for Fibrinopeptide A (FPA) ,etc. by FLIA (Flow Luminescence Immunoassay)

ArtNr LMB237Ra-96T
Hersteller Cloud-Clone
Menge 96 T
Kategorie
Typ Immunofluorescence Assays
Specific against Rat (Rattus norvegicus)
Sensitivity The minimum detectable dose of this kit is typically less than 9.767 pg/mL
ECLASS 10.1 32160701
ECLASS 11.0 32160701
UNSPSC 41116126
Alias FP-A
Lieferbar
Manufacturer - Applications
FLIA Kit for Antigen Detection.
Manufacturer - Category
FLIA Kit
Sample type
serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay length
3h
Method
Competitive Inhibition
Specificity

This assay has high sensitivity and excellent specificity for detection of Fibrinopeptide A (FPA) , etc. by FLIA (Flow Luminescence Immunoassay).

No significant cross-reactivity or interference between Fibrinopeptide A (FPA) , etc. by FLIA (Flow Luminescence Immunoassay) and analogues was observed.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Fibrinopeptide A (FPA) , etc. by FLIA (Flow Luminescence Immunoassay) were tested 20 times on one plate, respectively.

Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Fibrinopeptide A (FPA) , etc. by FLIA (Flow Luminescence Immunoassay) were tested on 3 different plates, 8 replicates in each plate.

CV(%) = SD/meanX100

Intra-Assay: CV<10%

Inter-Assay: CV<12%

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. Preparation of standards, reagents and samples before the experiment;

2. Add 50μL standard or sample to each well,

        add 10μL magnetic beads, and 50μL Detection Reagent A, incubate 90min at 37° C on shaker;

3. Wash plate on magnetic frame for three times;

4. Add 100μL prepared Detection Reagent B, and incubate 30 min at 37° C on shaker;

5. Wash plate on magnetic frame for three times;

6. Add 100μL sheath solution, swirl for 2 minutes, read on the machine.
Test principle
Analyte-specific antibodies are pre-coated onto color-coded microparticles. Microparticles, standards, Labeled antigen and samples are pipetted into wells and the immobilized antibodies bind the analytes of interest.A competitive inhibition reaction is launched between biotin labeled analytes of interest and unlabeled analytes of interest (Standards or samples) with the pre-coated antibody specific to analytes of interest. Following a wash to remove any unbound substances, Streptavidin-Phycoerythrin conjugate (Streptavidin-PE) is added to each well. A final wash removes unbound Streptavidin-PE and the microparticles are resuspended in buffer and read using the Luminex or Bio-Plex analyzer. The MFI developed is reverse
proportional to the concentration of analytes of interest in the sample.

Hinweis: Die dargestellten Informationen und Dokumente (Bedienungsanleitung, Produktdatenblatt, Sicherheitsdatenblatt und Analysezertifikat) entsprechen unserem letzten Update und sollten lediglich der Orientierung dienen. Wir übernehmen keine Garantie für die Aktualität. Für spezifische Anforderungen bitten wir Sie, uns eine Anfrage zu stellen.

Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 96 T
Lieferbar: In stock
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