Brief

Pertussis, also known as whooping cough, is a highly contagious respiratory infection caused by the bacterium Bordetella pertussis. Pertussis spreads easily from person to person mainly through droplets produced by coughing or sneezing. The disease is most dangerous in infants, and is a significant cause of disease and death in this age group.

 

Sansure kit is used to detect Bordetella pertussis DNA present in the nasopharyngeal swab specimens by applying PCR fluorescence probing technique. The detection result can be used as an aid in the diagnosis of bordetella pertussis.

Parameters

Product features	Parameter
Specimen Types	Nasopharyngeal swab
Technical Platform	Fast release technology Advanced magnetic beads technology
Anti-contamination system	UNG enzyme + dUTP system
Internal Control	Internal control plasmid
PCR Instruments	Mx3000P; ABI 7500; MA-6000; S-Q31A/S-Q31B; S-Q36A
Sensitivity	200 copies/mL
Obtained Certificates	NMPA, CE-IVDD etc.

Brief

The Human Coronavirus (MERS) is generally detectable in respiratory samples during the acute phase of infection. The Human Coronavirus (MERS) Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) can qualitatively detect HCoV-MERS in sputum, alveolar lavage fluid, and throat swabs, the test results can be used to assist in the diagnosis of patients infected with HCoV-MERS, providing a molecular diagnostic basis for coronavirus MERS infection. The test results of this kit are for clinical reference only, and should not be used as the sole criterion for clinical diagnosis. It is recommended to conduct a comprehensive analysis of the condition based on the patient's clinical manifestations and other laboratory tests.

Parameters

Product features	Parameter
Covering Genes	MERS-CoV Orf1b
Specimen Types	Sputum, alveolar lavage fluid, throat swab
Technical Platform	One-tube fast release technology Advanced magnetic beads technology
Internal Control Gene	RNase P
Compatible Instruments	ABI 7500, Stratagene Mx3000P, SLAN®-96P, MA-6000, iPonatic S-Q36A/S-Q31A/S-Q31B
Sensitivity	500 copies/mL
Qualification	CE

Brief

Mycobacterium tuberculosis (M. tuberculosis) is the pathogen causing tuberculosis, which can invade all organs of the whole body, and pulmonary tuberculosis caused by pulmonary involvement is the most common. Early diagnosis and treatment are crucial measures to effectively control the spread of tuberculosis.

 

Due to the abuse of antibiotics or the insufficient course of drugs of patients, the sensitivity of patients to drugs weakens or even disappears, resulting in the decreasing or ineffective effect of drugs on pulmonary tuberculosis. According to the types of anti-tuberculosis drugs, drug-resistant tuberculosis can be divided into monoresistance pulmonary tuberculosis, polyresistance pulmonary tuberculosis, multidrug resistance pulmonary tuberculosis and extensively drug-resistant pulmonary tuberculosis. Rifampicin is one of the first-line drugs for the treatment of pulmonary tuberculosis.

 

The Mycobacterium Tuberculosis and Rifampicin Resistance Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is a real-time polymerase chain reaction test kit intended for the qualitative detection of the nucleic acid of mycobacterium tuberculosis and rifampicin resistance mutations in human sputum samples. The test results can be used to assist in the diagnosis of TB patients and patients with an increased risk of RFP drug-resistant TB, providing a molecular diagnosis basis for infected patients.

Parameters

Product features	Parameter
Specimen Type	Sputum
Technical Platform	One-tube fast release technology
PCR Instruments	iPonatic Ⅲ (S-Q36A)
Internal Control	RNase P
Limit of detection	Mycobacterium tuberculosis 1,000 Bacteria/mL; Rifampicin resistance 10,000 Bacteria/mL

The kit is registered in Indonesia.

Brief

Mycoplasma pneumoniae (MP) is a pathogenic microorganism between bacteria and virus. It is mainly transmitted through buccal and nasal mucus by the air causing respiratory diseases, with the highest incidence in children and adolescents. Respiratory infection has the manifestations of pharyngitis and bronchitis, with a few cases causing infection to the lung. Recently, incidence among infants and children is increasing, therefore, early diagnosis and treatment can decrease the exacerbation of acute pneumonia in children. The development of molecular biology also draws more attention to the fluorescence quantitative PCR technology for the detection of MP-DNA.   This diagnostic kit is an in vitro nucleic acid amplification test for the detection of mycoplasma pneumoniae DNA in humansputum and throat swab. It is intended for use as an aid in the diagnosis of an MP infection and providing a molecular-diagnostics-based solution.

Parameters

Product features	Parameter
Specimen Type	Sputum and throat swab
Extraction Platform	One-tube fast release technology
Internal Control	cloning plasmid containing the target gene fragment
PCR Instrument	ABI 7500, SLAN-96P,MA-6000, Roche LightCycler 480, iPonatic S-Q31A&B,S-Q36A
Sensitivity	400 copies/mL
Spec.	48T, 12-P
Qualification	CE

Brief

Acute infectious disease caused by adenovirus, easily affects the mucous membranes of the respiratory and digestive tracts, the conjunctiva of the eyes, the urinary tract and the lymph nodes. The main manifestation is an acute upper respiratory tract infection. The population is generally susceptible, mostly the children. Infants are susceptible to adenovirus pneumonia, which is severe and has a high mortality rate. The source of infection is the patient and the latent infected person. The virus is excreted from the respiratory tract and conjunctival secretions, feces and urine, and is transmitted by airborne droplets, close contact and the feces-oral route.   The Adenovirus Nucleic Acid Diagnostic Kit is used for nucleic acid testing of adenovirus in patients suspected of being adenovirus infections (e.g., fever, cough, wheezing, dyspnea, bronchopneumonia, upper respiratory tract infections, lung infections, etc.) or related close contacts, and the results can be used to assist in the diagnosis of adenovirus infection and provide a molecular diagnostic basis for adenovirus infection.

Features

• High sensitivity: Detection sensitivity reaches 200 copies/mL.
• Quick and easy: Perfectly match Sansure's one-tube fast Sample Release Reagent, easy to operate.
• IC monitoring: IC(Internal Control) monitoring test process to avoid false negative results.

Parameters

Items	Parameter
Specimen Type	Throat swab
Extraction Platform	One-tube fast release technology Advanced magnetic beads technology
Anti-contamination system	UNG enzyme + dUTP system
PCR Instrument	ABI 7500; MA-6000; SLAN-96P; QuantStudio 5; iPonatic S-Q31A&B; S-Q36A
Sensitivity	200 copies/mL
Qualification	NMPA, CE

Brief

Mycobacterium tuberculosis virus (TB) is a pathogenic bacterium that causes tuberculosis. It is likely to infect all human tissues and organs, especially the lungs to cause pulmonary tuberculosis. Early diagnosis and treatment are important for effective control of tuberculosis.   In recent years, with the development of molecular biology, nucleic acid fluorescence quantitative PCR method based on the mycobacterium tuberculosis nucleic acid has drawn more and more attention from researchers.

Parameters

Product features	Parameter
Specimen Type	Human sputum
Extraction Platform	One-tube fast release technology
Internal Control	Cloning plasmid, without TB target sequence
PCR Instrument	ABI 7500, SLAN-96P,MA-6000, Stratagene Mx3000P, iPonatic S-Q31A&B,S-Q36A
Sensitivity	1 bacterium/mL
Spec.	48T, 12-P
Qualification	CE

Brief

The SARS-CoV-2 Rapid Antigen Test (Immunochromatography Assay) for self-testing is authorized for home use with self-collected nasal swab samples to directly detect antigen of SARS-CoV-2 virus. With the help of this kit, people without professional training can also easily acquire their COVID-19 test result within 15-20 minutes.

Features

• Accurate Sensitivity 94.55%, Specificity 100%
• Convenient No instrument needed, easy to operate
• Fast Result available in only 15-20 min
• Flexible Get tested anytime when you are free

Instruction

Result interpretation

Parameters

Qualification

CE

Kit components

No.	Product Name	Spec.
S3120E-1-H, S3120E-5-H	SARS-CoV-2 Rapid Antigen Test (Immunochromatography Assay)	1 Test, 5 Tests

The kit components:

•  SARS-CoV-2-Antigen Test Cassette (with desiccant)
• SARS-CoV-2 Sample Extraction Buffer
• Swab
• Plastic Waste Bag

Brief

The SARS-CoV-2 Rapid Antigen Test (Colloidal Gold Method) is intended for the qualitative detection of the SARS-CoV-2 nucleocapsid protein in human nasopharyngeal or nasal swab sampled from individuals suspected of COVID-19.

Parameters

Testing Time	10-15 minutes
Sensitivity	98.4%
Specificity	98.1%
Qualification	CE

Kit components

No.	Product Name	Spec.
S3109E-25	SARS-CoV-2 Rapid Antigen Test (Colloidal Gold Method)	25 tests

Brief

The SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple Nucleic Acid Diagnostic Kit (PCR-Fluorescence Probing) is a real-time RT-PCR test intended for the qualitative Diagnostic of nucleic acid from SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus Multiple in the nasopharyngeal swabs and oropharyngeal swabs from individuals.

 

As the seventh coronavirus that infects humans, the SARS-CoV-2 can cause fever, fatigue, dry cough, dyspnea and other symptoms. In severe cases, it can cause acute respiratory distress syndrome, septic shock, and even death. At the same time, the SARS-CoV-2 has a strong spreading ability and has a wide range. Influenza virus (Influenza virus) can cause acute respiratory infections, with clinical manifestations of fever, headache, myalgia, fatigue, rhinitis, sore throat and cough. Influenza viruses can aggravate underlying diseases (such as heart and lung diseases) or cause secondary bacterial pneumonia or primary influenza viral pneumonia. The elderly and people with various chronic diseases or physical weakness are prone to severe complications and mortality higher after infecting influenza. Respiratory syncytial virus (RSV) belongs to the Pneumovirus genus of the Paramyxoviridae family. It mainly causes lower respiratory tract infections such as bronchiolitis and pneumonia in infants under 6 months, as well as rhinitis , Cold and other upper respiratory tract infections in older children and adults.

Parameters

Product features	Parameter
Covering pathogens	SARS-CoV-2, Influenza Virus and Respiratory Syncytial Virus
Specimen Types	Nasopharyngeal swab and oropharyngeal swab
Technical Platform	One-tube fast release technology Advanced magnetic beads technology
Internal Control	RNase P gene
Compatible Instrument	ABI 7500; MA-6000; SLAN®-96P; iPonatic S-Q31A/S-Q31B/S-Q36A
Sensitivity	500 copies/mL.
Qualification	CE

Brief

COVID-19 is an infectious disease caused by a newly discovered coronavirus named SARS-CoV2.   Most people infected with the COVID-19 virus will experience mild to moderate respiratory illness and recover without requiring special treatment. Elder people, and those with underlying medical problems like cardiovascular disease, diabetes, chronic respiratory disease, and cancer are more likely to develop serious illness.   Sansure COVID-19 diagnostic solutions are used to directly detect  the presence of viral RNA, which will be detectable in patients before antibodies form or symptoms of the disease are present, which means the test results can tell whether or not that someone gets virus very early on in their illness.

Performance

• One-tube/fast release technology
• Up to 96 samples at one time
• Simple operation process, less specialist training
• Room temperature lysis, less contamination
• Sampling types : nasopharyngeal swab, oropharyngeal swab, alveolar lavage fluid, sputum, serum, whole blood ,Feces
• Enhance large-scale screening efficiency
• Internal control: human housekeeping gene RNase P

Parameters

Product features	Parameters
Specimen Type	Nasopharyngeal swab, oropharyngeal swab, alveolar lavage fluid, sputum, serum, whole blood, feces
Extraction Platform	One-tube fast release technology Advanced magnetic beads technology
Internal Control	Rnase P gene
PCR Instrument	ABI7500, QuantStudioTM 5, SLAN-96P, MA-6000, Bio-Rad CFX-96, QuantGene 9600, LightCycler 480, iPonatic S-Q31A&B,S-Q36A
Sensitivity	200 copies/mL
Spec.	24T, 48T, 24-P
Qualification	CE