Panadea CCHFV (NP) IgG ELISA Kit (ELG.001) - RUO
The Panadea CCHFV (NP) IgG ELISA Kit (Research Use Only) is intended for qualitative detection of IgG antibodies directed against the Crimean-Congo Hemorrhagic Fever Virus (CCHFV) nucleocapsid protein (NP).

The Panadea CCHFV (NP) IgG ELISA Kit (Research Use Only) allows the qualitative detection of human serum/plasma IgG antibodies directed against the Crimean-Congo Hemorrhagic Fever Virus (CCHFV) nucleocapsid protein (NP) in 96-well (12x8) format. The test is based on a patented immune complex capture principle.

Generalised kit image, content may vary
REF:
ELG.001
Intended use:

Determination of the presence/absence of IgG antibodies directed against CCHFV NP in human serum

Assay principle:

IgG immune complex ELISA utilizing patented CD32 capture technology

Kit format:

Microwell plate (96 tests)

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Quick facts

For whom is CCHFV surveillance important?

Surveillance of Crimean-Congo Hemorrhagic Fever Virus prevalence through screening of population samples for antibodies against the virus has importance not only for populations where the disease is known to circulate, but also for public health system preparedness on a world-wide level. As CCHFV can spread from person to person via contact of blood and other bodily fluids, the detection of the CCHF virus in a population is important for the prevention of outbreaks.

Why should IgG antibody detection be used to monitor CCHFV prevalence?

IgG antibodies persist in the blood of infected individuals long after the person has recovered from the viral infection. Surveillance studies employing IgG detection are critical for detecting CCHFV in human and ruminant populations without the requirement for the screened individuals to have clinically presented with suspicious symptoms and sampled during the transient period when they contain live virus. This makes IgG detection a valuable tool for observing the prevalence of a virus in a population, especially in Low- and Middle-Income Countries (LMIC), where infections with CCHFV are less likely to be correctly identified at the primary healthcare level.

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