Transport Package
Cartons
Production Capacity
100, 000/Day
Reference Price
$ 0.21 - 0.23
Description
Product Description
Shanghai Eugene Bio tech Co.,Ltd.(Eugene) was established in 2007,which is a subsidiary of CIRC (China Isotope&Radiation Corporation, stock code:01763.hk, dedicated to the research and production of colloidal gold, CLIA, ELISA, RIA and other rapid detection methods. Our headquarters is Beijing North Institute of Biological Technology (BNIBT), it was established on July01,1985, which has engaged in researching, producing and selling of in vitro diagnose kits. It's one of the biggest and earliest institutes of the field in China.
EUGENE series of human colloidal gold rapid detection products cover infectious diseases such as hepatitis, gastrointestinal, respiratory infections, tropical diseases, sexual transmitted diseases, fertility hormones and natal-healthcare, the rapid detection of tumor markers, cardiovascular disease markers, drugs and alcohol, and so on.
Eugene products are widely used in domestic and foreign hospitals, clinics, physical examination centers, disease prevention and control systems, epidemic prevention stations, blood stations, family, laboratories, research institutions, public security and traffic system, etc. We have exported to more than 50 countries in the world, won the consistent praise of the majority of users with excellent performance and excellent service.
We Eugene mainly contribution to the human health.As we had supported the Dengue fever epidemic of Bangladesh in 2023.
Our Cox-19 test had been registered in Italy,Indonesia,and exported to many countries of the Global market, and receive the good reputation and good feedback by all of our customers.
The EUGENE
®
Anti-HCV rapid test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of antibodies to Hepatitis C virus (Anti-HCV) in human whole blood, serum or plasma. It is intended for the screening of blood and blood products to be used for transfusion and as an aid in the diagnosis of infection with HCV. The test is recommended for professional use only. All results must be interpreted together with other clinical information or other diagnosis methods available to the physician.
Hepatitis C is an
infectious disease
primarily affecting the
liver
, caused by the
hepatitis C virus
(HCV).
1
The infection is often
asymptomatic
, but chronic infection can lead to scarring of the liver and ultimately to
cirrhosis
, which is generally apparent after many years. In some cases, those with cirrhosis will go on to develop liver failure or other complications, including
liver cancer
or life-threatening
esophageal varices
and
gastric varices
.
1
Hepatitis C virus is a single stranded RNA virus with some structural relations to the flavivirus family. Nucleic acid sequences of HCV cDNA clones provided the basis for the construction of recombinant peptides representing putative Hepatitis C virus proteins.
2
In recent study, proteins of core, NS3, NS4, and NS5 were found to be highly immunogenic among 11 types of Hepatitis C virus proteins.
3-5
Compared to the earlier generations of HCV test using single or double recombinant antigens, the EUGENE
®
Anti-HCV rapid test uses multiple recombinant proteins to detect antibodies, so as to obtain an improved sensitivity and specificity.
I
NTERPRETATION OF RESULTS
NEGATIVE RESULT:
If only the C band is developed, the test indicates that no detectable antibodies to HCV present in the specimen. The result is negative.
POSITIVE RESULT:
If both C and T bands are developed, the test indicates for the presence of antibodies to HCV in the specimen. The result is positive.
The intensity of the color in the test line region (T) may vary depending on the concentration of antibodies to HCV present in the specimen. Therefore, any shade of color in the test region (T) should be considered positive.
Samples with positive results should be confirmed with alternative testing method(s) and clinical findings before a positive determination is made.
INVALID:
If no C band is developed, the assay is invalid regardless of color development on the T band as indicated below. Repeat the assay with a new device.
If the problem persists, discontinue using the kit immediately and contact your local distributor.
Disposable Medical Supplies
PNEUTEC.IT, 2023