Colloidal Gold · Hepatitis
HCV Ab Detection Kit (Colloidal Gold)
Qualitative detection of antibodies to hepatitis C virus (HCV) in human serum or plasma. Intended as an aid in the diagnosis of HCV infection and for screening in high-prevalence populations.
- SKU Code
AENE-HP013AB- Approval
- On request
- Product Type
- Assay / Kit
- Status
- Available
Qualitative detection of antibodies to hepatitis C virus (HCV) in human serum or plasma. Intended as an aid in the diagnosis of HCV infection and for screening in high-prevalence populations.
| Product type | Assay / Kit |
|---|---|
| Technology platform | Colloidal Gold |
| Application area | Hepatitis |
Epidemiology
Hepatitis C is caused by the hepatitis C virus (HCV), a single-stranded RNA virus from the Flaviviridae family. This chronic condition currently affects an estimated 130–170 million people worldwide.
According to World Health Organization data, over 350,000 fatalities from HCV-related liver disease occur each year, and roughly 3 to 4 million new infections are acquired annually. It is estimated that around 3% of the global population is infected with HCV, with more than 80% of those individuals progressing to chronic liver disease. After 20–30 years, cirrhosis develops in 20–30% of cases, and 1–4% ultimately die from cirrhosis or liver cancer.
| SKU code | AENE-HP013AB |
|---|---|
| Target region | HCV Ab |
| Storage temperature | 4℃-30℃ |
| Sample type | Human serum and plasma |
| Shelf life | 24 months |
| Auxiliary instruments | Not required |
| Extra Consumables | Not required |
| Detection time | 10-15 mins |
| Specificity | Use the kits to test the interfering substances with the following concentrations, and the results should not be affected. |
| Approval | On request |
|---|---|
| Documents | Datasheet, IFU, SDS, COA / conformance, origin, and export documents where available |
FAQ
What should be confirmed before quotation?
Sample context, collection method, and extraction workflow should be confirmed before final kit selection.
Which documents can be requested?
Datasheet, IFU, SDS, COA / conformance, origin, insurance, and export documents can be checked where available.
Can the format be adjusted for different workflows?
Liquid or lyophilized format options should be confirmed together with instrument compatibility and shipment requirements.
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