CE Magnetic Bead Method Nucleic Acid Extraction and Purification Kit
It's designed for the rapid, efficient and automatic isolation and purification of high quality virus nucleic acid from a variety of samples on the automatic nucleic acid extraction system.
Features:
1): Rapid and Reliable: Fast procedures and easy to use
2): High Sensitivity
3): High Efficiency: â?¥ 95% of the nucleic acid can be combined.
4): Versatile: Nucleic acid of various virus, Hepatitis, etc. in different samples, such as Serum, Plasma, Whole blood, Swabs, Saliva, Body fluid, Tissue, Feces, BALF, etc. for a broad range of down stream applications.
5): Safe: Non-toxic
â?¢Get result rapidly (10 min), suitable for large-scale screening.
â?¢Easy to operate, no instrument needed.
â?¢Detect virus directly, faster than PCR test
â?¢High accuracy and good consistency with PCR test
â?¢Room-temperature storage (4â??- 30â??)
Production Description:
The double antibody sandwich method is adopted in the product, and measurement is conducted in the form of solid-phase immune chromatography. The sample to be tested will diffuse upwards at the charging end under capillary action, and then SARS-CoV-2 antigen in the sample will combine with the antibody in the marker pad and form colloidal gold antibody-antigen complex; The complex continues to diffuse to the nitrocellulose membrane with the sample, and then blocked by T-line (test line) packed with antibody, and form colloidal gold labeled antibody-antigen-immune complex packed with antibody. The rest unblocked colloidal gold complex continues to move upwards, and combine with C-line (quality control line), indicating that the reaction is completed.
Simple and fast : extraction within 20min, no centrifuge and can be used for automated extraction
Safer : quickly inactivate viruses during extraction
Wide used : extracting highly pure viral nucleic acid (DNA/RNA) from samples such as human nasopharyngeal swabs, sputum, broncho lavage fluid and alveolar lavage fluid
High yield: high nucleic acid extraction efficiency, making downstream detection more sensitive
High purity : Maximum removal of inhibitory impurities, high purity nucleic acid obtained can be directly used for downstream detection
Production Description
This product is used for the steps of nucleic acid extraction, enrichment and purification. This kit is applicable for extracting highly pure viral nucleic acid (DNA/RNA) from samples such as human nasopharyngeal swabs, sputum, broncho lavage fluid and alveolar lavage fluid. The obtained nucleic acid can be used in the clinical in vitro testing.
HIGH YIELD
Using magnetic beads method virus DNA / RNA extraction kit (Vazyme # RM102) and another virus extraction kit (from TI company) to extract nucleic acids from four samples, namely SARS-CoV-2 pseudovirus, African swine fever virus 3(ASFV), Porcine Epidemic Diarrhea Virus (PEDV) and HEK293 cells, and detected by qPCR detection. From the test results, it can be seen that The Ct value of the RNA extracted by the virus DNA / RNA extraction kit (Vazyme # RM102) is 1-3 lower, indicating the efficiency of Vazyme # RM102 is higher than other brands of similar virus extraction kits.
Wide compatibility
Using the virus DNA / RNA extraction kit (Vazyme # RM102) to extract the SARS-CoV-2 pseudovirus with an initial amount of 10-100000 copies, , then detected by the new coronavirus (SARS-CoV-2) nucleic acid detection kit. The test results show that the extraction kit is wide compatibility.
Storage
15 ~ 25�°C,
It is recommended to store the magnetic beads at 2 ~ 8�°C.
Please be noted the beads shall not be stored below 0�°C.
PERFORMANCE SPECIFICATIONS
1. Detection limitation: 200 copies /mL.
2. Precision: using precision reference CV1 and CV2 for within-batch and
between-batch detection, the coefficient of variation (CV) of their Ct values
is â?¤ 5.0%.
3. Conformity rate of Negative Control: 100%
4. Conformity rate of Positive Control: 100%
5. Specificity: This product will not cross react with positive samples of
human coronavirus HKU1 OC43, NL63 and 229E, SARS coronavirus, MERS
corona-virus, H1N1 (new influenza A (H1N1) virus (2009), the seasonal
H1N1) and H3N2, H5N1, H7N9, influenza B Yamagata, Victoria, respiratory
syncytial virus type A, B, parainfluenza type 1, 2, 3, rhinovirus species A, B
and C, adenovirus, 1, 2, 3, 4, 5, 7 and 55, enterovirus species A, B, C,
D,Human pulmonary virus, partial pulmonary virus, EB virus, measles virus,
human cytomegalo virus, rotavirus, norovirus, mumps virus, varicella-zoster
virus and mycoplasma pneumoniae, chlamydia pneumoniae, legionella,
bordetella pertussis, haemophilus influenzae, staphylococcus aureus,
streptococcus pneumoniae, pyogenic streptococcus, klebsiella pneumoniae,
mycobacterium tuberculosis, pyogenic streptococcus, candida albicans,
candida glabrata, newborn Cryptococcus and human genome DNA.
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This kit works by immune chromatography. The sample moves with capillary
action to move forward along the test card. If the sample contains novel
coronavirus antigen, the antigens will bind with colloidal gold labeling will be
coronavirus monoclonal antigen, the immune complex will be membrane fixed
will be coronavirus monoclonal antibody capture, form the purple line, display
will be coronavirus antigen positive; If the line does not show color, the negative
result will be displayed. The test card also contains a quality control line C, which
shall appear in magenta regardless of whether there is a detection line.
All check COVID-19 lgG/lgM Is a rapid immunochromatographic test for the qualitative detection of IgM and IgG Antibodies to the SARS-CoV-2 in human serum, plasma, venous or capillary whole blood. Results from the AllCheck COVID-19 IgG/IgM should not be used as the sole basis for diagnosis.
1. Rapid testing for SARS-CoV-2 antibodies within 10 minutes
2. Just 10L of specimen : serum, plasma or whole blood
3. Suitable for Point-of-Care testing
4. No need for extra equipment
5. Material provided : Device, Sample diluent
6. CE approved.
Covid-19 Antibody IgM/IgG Rapid Test kit,
Using whole blood, Serum, Plasma sample, take less than 10 minutes,
a lateral flow immunochromatographic assay for detaction of SAR-CoV-2 IgM/IgG
antibodies in human blood specimens.
Package Unit: 25 tests/kit
25 test devices
1 Assay buffer
25 blood transfer pipettes
SLS Bio develops pharmaceuticals, diagnostic reagents, biological agents, diagnostic test instruments, and other related products. The company's testing kit for COVID-19 has +90% sensitivity and 96% specificity.
The outbreak of the novel coronavirus (COVID-19) rapidly transmit all over China and lots of countries. Although molecular test (RT-PCR) has become the standard method for diagnosis of this disease, the method has many limitations. In addition, the high false negative rates were reported. There is an urgent need for an accurate and rapid testing method that quickly identify large number of infected patients and asymptomatic carriers to prevent virus transmission and assure timely treatment of patients. GenBody COVID-19 IgM/IgG device is a chromatographic immunoassay kit for the rapid and differential detection of immunoglobulin M (lgM) and immunoglobulin G (IgG) against COVID-19 using serum, plasma and whole blood.
The outbreak of the novel coronavirus (COVID-19) rapidly transmit all over China and lots of countries. Although molecular test (RT-PCR) has become the standard method for diagnosis of this disease, the method has many limitations. In addition, the high false negative rates were reported. There is an urgent need for an accurate and rapid testing method that quickly identify large number of infected patients and asymptomatic carriers to prevent virus transmission and assure timely treatment of patients. GenBody COVID-19 IgM/IgG device is a chromatographic immunoassay kit for the rapid and differential detection of immunoglobulin M (lgM) and immunoglobulin G (IgG) against COVID-19 using serum, plasma and whole blood.
Warranty:2 years, 2 Years After-sale Service:Online Technical Support Material:Plastic Shelf Life:2 years Quality Certification:CE Instrument classification:Class II Safety standard:MFDS Product name:antibody test Sensitivity: >85% Specificity: >90% Total coincidence rate: >90% Work environmental temperature: 40 Inspection method:antibody detection Sample dosage:10ul Inspection time: 15min Type of sample:capillary vessel or vein
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