Human Dengue Early ELISA Kit

Referentie MBS018868-5x96

Formaat : 5x96-Strip-Wells

Merk : MyBiosource


Dengue Early (DE) ELISA Kit for Human

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS018868

Intended Uses: The kit uses a sandwich enzyme-linked immunosorbent assay (ELISA) to qualitatively analyze Human Dengue Early (DE) in Human serum, plasma. This kit is in vitro research use only! Not for therapeutic or test applications!Principle of the Assay:… More details

Product Overview

Online Datasheet in PDF
Product Name
Dengue Early, ELISA Kit
Full Product Name
Human Dengue Early ELISA Kit
Product Gene Name
DE elisa kit
Species Reactivity
Human
Assay Type
Qualitative Sandwich
Samples
Serum, plasma
Preparation and Storage
Store all reagents at 2-8 degree C
Inter-assay Precision
Inter-assay CV (?) are less than 15%.
Intra-assay Precision
Intra-assay CV (%) are less than 15%.

Other Notes

Small volumes of DE elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Searchable Terms for DE purchase

MBS018868 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Dengue Early, ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing DE. The ELISA analytical biochemical technique of the MBS018868 kit is based on DE antibody-DE antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect DE antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, DE. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).