High Accuracy Cmv Cytomegalovirus Antibody Test Igm
China High Accuracy Cmv Cytomegalovirus Antibody Test Igm, Find details about China Antibody Test, 19 Antibody from High Accuracy Cmv Cytomegalovirus Antibody Test Igm
Basic Info.
Model NO.
KWS0001
Model NO.
KWS0001
Product Desciption
Overview
Quick Details
Place of Origin:China
Power Source:Manual
Warranty:2 years, 24months
After-sale Service:Online technical support
Material:plastic, Paper
Shelf Life:2 years
Quality Certification:MSDS
Instrument classification:Class II
Product name:CMV Cytomegalovirus Antibody Test IgM
Format:Cassette
Specimen:Serum/Plasma/Whole Blood
Dimension:4mm
Package:25tests/box
Sensitivity:98.91%
Storage:4-30'C
Certificate:ISO13485
Safety standard:ISO13485
Supply Ability
Supply Ability:200000 Box/Boxes per Month
Packaging & Delivery
Packaging Details
1test/punch; 25tests/box
Port
Any port of China
1test/punch; 25tests/box
Port
Any port of China
Lead Time :
| Quantity(Pieces) | 1 - 500000 | >500000 |
| Est. Time(days) | 10 | To be negotiated |
Product Description
PRODUCT NAME
(CMV) Cytomegalovirus IgM Antibody Rapid Test Kit (Immunochromatography)
INTENDED USE
The reagent is used to detect the cytomegalovirus IgM antibody in serum /plasma qualitatively.It is used as an aid in the diagnostic of past infection and epidemiological investigation.
PRINCIPLE
The test utilizes antibodies including a recombinant CMV antigen and goat anti-mouse IgG antibody on the nitrocellulose membrane with colloidal gold marked anti-human IgM as a mark tracer. The reagent is used to detect the CMV IgM according to the principle of capture method and gold immunochromatography assay. The sample mixing up anti-human IgM-marker move along the membrane to the T line, and form the T line with recombinant CMV antigen when the sample contains CMV IgM, which is a positive result. Conversely, it is a negative result.
MAIN COMPONENTS
Basic components: Sample pad, colloidal gold marked pad, nitrocellulose membrane, absorbent paper and PVC board. Colloidal gold marked pad coated with anti-human IgM, nitrocellulose membrane coated with recombinant CMV antigen,control line coated with goat anti-mouse IgG antibody.
STORAGE AND EXPIRY
Store as packaged in the sealed pouch at 4-30°C, keep out of hot and direct sunlight, keep in dry place, valid for 24 months. DO NOT FREEZE. Some protective measures should be taken in hot summer and cold winter to avoid high temperature or freeze-thaw. The product is humidity-sensitive and should be used immediately after being opened. Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers or reagents can lead to false results.
Detailed Images
Limitations
1. This reagent is designed for the qualitative screening test. Concentration of analytes cannot be determined by this qualitative test.
2. The results of the reagent are only for clinical reference, which is not the only basis for clinical diagnosis and treatment. A confirmed diagnosis and treatment should only be made by a physician after all clinical and laboratory findings have been evaluated.
3. Negative result may occur when detecting short-term infected samples, indicate that the specific antibodies of CMV does not exist or the concentration is below detection limit. If CMV infection is still suspected, the sample should be collected 2 weeks later and carry the parallel detection with the first sample.
4. Negative results may occur at the beginning of acute infection, other testing method and analysis with clinical symptoms are suggested.
5. Results of patients who used to receive immunosuppressive therapy or with immune function damage (for example HIV), may have a low serology reference value.
6. Positive results of the patients who used to receive blood transfusions or other blood products therapy, should be analyzed cautiously.
PRODUCT NAME(CMV) Cytomegalovirus IgM Antibody Rapid Test Kit (Immunochromatography)
INTENDED USE
The reagent is used to detect the cytomegalovirus IgM antibody in serum /plasma qualitatively.It is used as an aid in the diagnostic of past infection and epidemiological investigation.
PRINCIPLE
The test utilizes antibodies including a recombinant CMV antigen and goat anti-mouse IgG antibody on the nitrocellulose membrane with colloidal gold marked anti-human IgM as a mark tracer. The reagent is used to detect the CMV IgM according to the principle of capture method and gold immunochromatography assay. The sample mixing up anti-human IgM-marker move along the membrane to the T line, and form the T line with recombinant CMV antigen when the sample contains CMV IgM, which is a positive result. Conversely, it is a negative result.
MAIN COMPONENTS
Basic components: Sample pad, colloidal gold marked pad, nitrocellulose membrane, absorbent paper and PVC board. Colloidal gold marked pad coated with anti-human IgM, nitrocellulose membrane coated with recombinant CMV antigen,control line coated with goat anti-mouse IgG antibody.
STORAGE AND EXPIRY
Store as packaged in the sealed pouch at 4-30°C, keep out of hot and direct sunlight, keep in dry place, valid for 24 months. DO NOT FREEZE. Some protective measures should be taken in hot summer and cold winter to avoid high temperature or freeze-thaw. The product is humidity-sensitive and should be used immediately after being opened. Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers or reagents can lead to false results.
Detailed Images
Limitations1. This reagent is designed for the qualitative screening test. Concentration of analytes cannot be determined by this qualitative test.
2. The results of the reagent are only for clinical reference, which is not the only basis for clinical diagnosis and treatment. A confirmed diagnosis and treatment should only be made by a physician after all clinical and laboratory findings have been evaluated.
3. Negative result may occur when detecting short-term infected samples, indicate that the specific antibodies of CMV does not exist or the concentration is below detection limit. If CMV infection is still suspected, the sample should be collected 2 weeks later and carry the parallel detection with the first sample.
4. Negative results may occur at the beginning of acute infection, other testing method and analysis with clinical symptoms are suggested.
5. Results of patients who used to receive immunosuppressive therapy or with immune function damage (for example HIV), may have a low serology reference value.
6. Positive results of the patients who used to receive blood transfusions or other blood products therapy, should be analyzed cautiously.
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Packing & Delivery
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