Other Infections – Sansure Biotech https://www.sansureglobal.com Innovating Diagnostics for All Wed, 15 Nov 2023 02:24:05 +0000 en-US hourly 1 https://wordpress.org/?v=6.6.1 S3352E MPXV – Monkeypox virus Nucleic Acid Diagnostic Kit https://www.sansureglobal.com/product/s3352e-mpxv/?utm_source=rss&utm_medium=rss&utm_campaign=s3352e-mpxv https://www.sansureglobal.com/product/s3352e-mpxv/#respond Thu, 26 May 2022 00:59:40 +0000 https://www.sansureglobal.com/?post_type=product&p=4059 Brief Monkeypox is a disease of global public health importance as it not only affects countries in west and central Africa, but the rest of the world. Human-to-human transmission can result from close contact with respiratory secretions, skin lesions of an infected person or recently contaminated objects. Transmission via droplet respiratory particles usually requires prolonged face-to-face contact, which puts health workers, household members and other close contacts of active cases at greater risk.   WHO recommends polymerase chain reaction (PCR) is the preferred laboratory test given its accuracy and sensitivity.

Performance

  • Test time ≤ 30 min
  • Sensitivity: 200 copies/mL
  • Suitable for PCR and iPonatic

Parameters

Items Parameters
Specimen Type Vesicles or pustules, nasopharyngeal swab, oropharyngeal swab, serum, whole blood
Extraction Platform One-tube fast release technology Advanced magnetic beads technology
Internal Control Human gene
PCR Instrument ABI 7500, QuantStudio™ 5, LightCycler 480, MA-6000, SLAN-96P, QuantGene 9600, Portable Molecule Workstation S-Q31A&B, Portable Molecular Workstation S-Q36A
Sensitivity 200 copies/mL
Spec. 48 T, 12-P
Qualification CE
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S3014E HCMV – Human Cytomegalovirus DNA Quantitative Fluorescence Diagnostic Kit https://www.sansureglobal.com/product/s3014e-hcmv/?utm_source=rss&utm_medium=rss&utm_campaign=s3014e-hcmv https://www.sansureglobal.com/product/s3014e-hcmv/#respond Thu, 22 Jul 2021 08:03:00 +0000 http://v2.sansureglobal.com/?post_type=product&p=3166 Brief Human cytomegalovirus (HCMV), also called cell inclusion body virus, is a double helix DNA virus and belongs to β genus of herpes virus family, which causes infected cells to enlarge and has a huge intranuclear inclusion. The ways of infection of HCMV is mainly through contact, blood transfusion, intrauterine and birth canal, and the infections are commonly found in fetus, newborns, pregnant women, etc. If the pregnant women are infected, it may cause their newborns congenital monstrosity. When the organism immune deficiency or immune system is under inhibitory state, people can be easily infected by HCMV, such as the patients receiving immunosuppressive therapy after transplantation of organ, the patients receiving malignant tumor chemotherapy and AIDS patients, etc. If these patients are infected by HCMV, it usually causes high mortality and serious diseases.   Clinical tests suggest that HCMV infection hasn’t specific manifestations and it causes harm to multiple organs, especially the liver and lung. A statistical analysis of positive and negative rate of HCMV in various kinds of clinical indications shows HCMV infection is probably related with various diseases, such as Cytomegalovirus hepatitis, Infant hepatitis syndrome, liver dysfunction, pneumonia, Bronchitis, Upper respiratory tract infections, enteritis, enterocolitis, diarrhea, hematemesis, heart failure, etc.   The Human Cytomegalovirus DNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) is an in vitro nucleic acid amplification test for the detection of HCMV DNA in human urine, serum and peripheral blood samples. It is intended for use as an aid in the diagnosis of an HCMV infection and for observing drug efficacy.

Parameters

Product features Parameter
Specimen Type urine, serum, and peripheral blood.
Technical Platform One-tube fast release technology Advanced magnetic beads technology
Target pathogen HCMV
Internal Control cloning plasmid
PCR Instrument ABI7500, Roche LC 480 and Stratagene Mx3000P
Amplification Time 70 min
Sensitivity 400 copies/mL
Spec. 48T
Qualification CE
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S3015E EBV – Epstein-Barr virus DNA Quantitative Fluorescence Diagnostic Kit https://www.sansureglobal.com/product/s3015e-ebv/?utm_source=rss&utm_medium=rss&utm_campaign=s3015e-ebv https://www.sansureglobal.com/product/s3015e-ebv/#respond Thu, 22 Jul 2021 08:02:31 +0000 http://v2.sansureglobal.com/?post_type=product&p=3165 Brief Epstein-barr virus (EBV) is known to be the first virus that is definitely related with human tumors. EBV infection mainly causes infectious mononucleosis in children and tumor-related diseases such as Burkitt’s lymphoma, lymphoid tissue hyperplasia in immunocompromised individuals, primary lymphoma, empyema associated lymphoma, T-cell lymphoma, NK cell lymphoma/leukemia, Hodgkin’s disease, nasopharyngeal carcinoma, stomach cancer, lymphoid epithelial tissue cancer, smooth muscle tumors, etc.   The Epstein-Barr virus DNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) is an in vitro nucleic acid amplification test for the quantification of Epstein-Barr Virus (EBV) DNA in peripheral blood. Test result can be used as an aid in the diagnosis of an EBV infection and in observation of drug efficacy.

Parameters

Product features Parameter
Specimen Type peripheral blood.
Technical Platform One-tube fast release technology Advanced magnetic beads technology
Target pathogen EBV
Internal Control cloning plasmid
PCR Instrument ABI7500, Roche LC 480 and Stratagene Mx3000P
Amplification Time 70 min
Sensitivity 400 copies/mL
Spec. 48T
Qualification CE
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