CLIA Kit for Folic Acid (FA) View larger

CLIA Kit for Folic Acid (FA)

CC-CCA610Ge

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 39.1-10,000pg/mL
Sensitivity The minimum detectable dose of this kit is typically less than 16.4pg/mL
Research Area Hematology
Organism species Pan-species (General)
Alternative Names VB9
Item Name Folic Acid
Assay Length 2h
Method Competitive Inhibition
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 a monoclonal antibody specific to Folic Acid (FA). A competitive inhibition reaction is launched between biotin labeled Folic Acid (FA) and unlabeled Folic Acid (FA) (Standards or samples) with
Assay procedure summary 1. Prepare all reagents, samples and standards
UniProt ID -

More info

Especificidad:

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

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Folic Acid (FA) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Folic Acid (FA) 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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