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- Cytomegalovirus(CMV) IgG/IgM Rapid Test
- Product Detail
- Company Profile
- For professional in vitro diagnostic use only. Do not use after expiration date.
- Do not eat, drink or smoke in the area where the specimens and kits are handled.
- Handle all specimens as if they contain infectious agents.
- Observe established precautions against microbiological hazards throughout all procedures and follow the standard procedures for proper disposal of specimens.
- Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed.
- Follow standard biosafety guidelines for handling and disposal of potential infective material.
- Humidity and temperature can adversely affect results.
- The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
- The test must remain in the sealed pouch until use.
- Do not freeze.
- Cares should be taken to protect components in this kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipments, containers or reagents can lead to false results.
- The One Step CMV IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is intended only for use with human whole blood, serum or plasma specimens.
- Only clear, non-hemolyzed specimens are recommended for use with this test. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures.
- Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20℃. Whole blood should be stored at 2-8℃ if the test is to be run within 2 days of collection. Do not freeze whole blood specimens.
- Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
- Pack the specimens in compliance with applicable regulations for transportation of etiological agents, in case they need to be shipped.
- Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
- Internal procedural controls are included in the test. A colored band appearing in the control region (C) is considered an internal positive procedural control. It confirms sufficient specimen volume and correct procedural technique.
- External controls are not supplied with this kit. It is recommended that positive and negative controls be tested as a good laboratory practice to confirm the test procedure and to verify proper test performance.
- Choo, Q.L., G. Kuo, A.J. Weiner, L.R. Overby, D.W. Bradley, and M. Houghton. Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome. Science 1989; 244:359
- Kuo, G., Q.L. Choo, H.J. Alter, and M. Houghton. An assay for circulating antibodies to a major etiologic Virus of human non-A, non-B hepatitis. Science 1989; 244:362
- van der Poel, C. L., H.T.M. Cuypers, H.W. Reesink, and P.N.Lelie. Confirmation of hepatitis C Virus infection by new four-antigen recombinant immunoblot assay. Lancet 1991; 337:317
- Wilber, J.C. Development and use of laboratory tests for hepatitis C infection: a review. J. Clin. Immunoassay 1993; 16:204
- Krick, J.A. and Remington, J.S.: Toxoplasmosis in the adult: An Overview. New Eng. J. Med. 298:550-553, 1978
- Anderson, S.E. and Remington, J.S.: The diagnosis of Toxoplasmosis. So. Med. J. 68:1433-1443, 1975.
- Feldman, H.A.: Toxoplasmosis: An overview. Bull. N.Y. Acad. Med. 50:110-127, 1974.
- Wilson, C.B., Remington, J.S., Stagno, S. and Retnolds, D.W.: Development of adverse sequelae in children born with subclinical congenital Toxoplasma infection. Pediatrics 66:767-774, 1980.
- For professional in vitro diagnostic use only. Do not use after expiration date.
- Do not eat, drink or smoke in the area where the specimens and kits are handled.
- Handle all specimens as if they contain infectious agents.
- Observe established precautions against microbiological hazards throughout all procedures and follow the standard procedures for proper disposal of specimens.
- Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are assayed.
- Follow standard biosafety guidelines for handling and disposal of potential infective material.
- Humidity and temperature can adversely affect results.
- The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
- The test must remain in the sealed pouch until use.
- Do not freeze.
- Cares should be taken to protect components in this kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipments, containers or reagents can lead to false results.
- The One Step CMV IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is intended only for use with human whole blood, serum or plasma specimens.
- Only clear, non-hemolyzed specimens are recommended for use with this test. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures.
- Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20℃. Whole blood should be stored at 2-8℃ if the test is to be run within 2 days of collection. Do not freeze whole blood specimens.
- Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
- Pack the specimens in compliance with applicable regulations for transportation of etiological agents, in case they need to be shipped.
- Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
- Internal procedural controls are included in the test. A colored band appearing in the control region (C) is considered an internal positive procedural control. It confirms sufficient specimen volume and correct procedural technique.
- External controls are not supplied with this kit. It is recommended that positive and negative controls be tested as a good laboratory practice to confirm the test procedure and to verify proper test performance.
- Choo, Q.L., G. Kuo, A.J. Weiner, L.R. Overby, D.W. Bradley, and M. Houghton. Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome. Science 1989; 244:359
- Kuo, G., Q.L. Choo, H.J. Alter, and M. Houghton. An assay for circulating antibodies to a major etiologic Virus of human non-A, non-B hepatitis. Science 1989; 244:362
- van der Poel, C. L., H.T.M. Cuypers, H.W. Reesink, and P.N.Lelie. Confirmation of hepatitis C Virus infection by new four-antigen recombinant immunoblot assay. Lancet 1991; 337:317
- Wilber, J.C. Development and use of laboratory tests for hepatitis C infection: a review. J. Clin. Immunoassay 1993; 16:204
- Krick, J.A. and Remington, J.S.: Toxoplasmosis in the adult: An Overview. New Eng. J. Med. 298:550-553, 1978
- Anderson, S.E. and Remington, J.S.: The diagnosis of Toxoplasmosis. So. Med. J. 68:1433-1443, 1975.
- Feldman, H.A.: Toxoplasmosis: An overview. Bull. N.Y. Acad. Med. 50:110-127, 1974.
- Wilson, C.B., Remington, J.S., Stagno, S. and Retnolds, D.W.: Development of adverse sequelae in children born with subclinical congenital Toxoplasma infection. Pediatrics 66:767-774, 1980.
- Always best of all and always pay attention to innovation.
- Special customized service tightly following customers’ requests.
- Integrated excellent quality, competitive prices and super service together.
Cytomegalovirus(CMV) IgG/IgM Rapid Test
Cat. No.: RH0536X
SPECIMEN: Whole Blood/ Serum/ Plasma
INTENDED USE
The One Step CMV IgG/IgM Rapid Test Device is a rapid qualitative lateral flow test designed for the quantitive detection of IgG and IgM antibodies to Cytomegalovirus (CMV) in human Whole blood, serum or plasma samples.
INTRODUCTION
Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients.
PRINCIPLE
The One Step CMV IgG/IgM Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to CMV in Whole blood, Serum or Plasma. Each test consists of: 1) a burgundy colored conjugate pad containing CMV recombinant envelope antigens conjugated with Colloid gold (CMV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-CMV, T2 band is coated with antibody for the detection of IgG anti-CMV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-CMV, if present in the specimen, will bind to the CMV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a CMV IgG positive test result and suggesting a recent or repeat infection. IgM anti-CMV if present in the specimen will bind to the CMV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a CMV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.
KIT COMPONENTS
| Individually packed test devices | Each device contains a strip of CMV with colored conjugates and reactive reagents pre-spreaded at the corresponding regions. |
| Disposable pipettes | For adding specimens use. |
| Buffer | Phosphate buffered saline and preservative. |
| Package insert | For operation instruction. |
| Specimen collection container | For specimens collection use. |
| Timer | For timing use. |
| Centrifuge | For preparation of clear specimens |
PRECAUTIONS
STORAGE AND STABILITY
SPECIMEN COLLECTION AND STORAGE
PROCEDURE
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
1.Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2.Place the test device on a clean and level surface.
3.Hold the dropper vertically and transfer 1 drop of Plasma/serum specimen (approximately 10μl) or 2 drops of whole blood specimen (approximately 20μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below.
4.Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Notes: Applying sufficient amount of specimen is essential for a valid test result. If migration (the wetting of membrane) is not observed in the test window after one minute, add one more drop of buffer to the specimen well.
INTERPRETATION OF RESULTS
POSITIVE RESULT : IgM Positive: * The colored line in the control line region (C) appears and a colored line appears in test line region1 (T1).The result indicates the presence of CMV specific IgM antibodies.
IgG Positive: * The colored line in the control line region (C) appears and a colored line appears in test line region 2 (T2). The result indicates the presence of CMV specific IgG antibodies.
IgG and IgM Positive: * The colored line in the control line region (C) appears and two colored lines should appear in test line regions 1 and 2 (T1 and T2). The color intensities of the lines do not have to match. The result indicates that the presence of both CMV specific IgG and IgM antibodies.*NOTE: The intensity of the color in the test line region(s) (T1 and/or T2) will vary depending on the concentration of CMV antibodies in the specimen. Therefore, any shade of color in the test line region(s) (T1 and/or T2) should be considered positive.
NEGATIVE RESULT:
The colored line in the control line region (C) appears. No line appears in test line regions 1 or 2 (T1 or T2).
Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
The colored line in the control line region (C) appears. No line appears in test line regions 1 or 2 (T1 or T2).QUALITY CONTROL
LIMITATIONS OF THE TEST
1.The One Step CMV IgG/IgM Rapid Test Device is for in vitro diagnostic use only. The test should be used for the detection of CMV antibodies in Whole Blood /Serum / Plasma specimens only. Neither the quantitative value nor the rate of increase in CMV antibodies can be determined by this qualitative test.
2.The One Step CMV IgG/IgM Rapid Test Device will only indicate the presence of CMV antibodies in the specimen and should not be used as the sole criteria for the diagnosis of CMV infection.
3.As with all diagnostic tests, all results must be interpreted together with other clinical information available to the physician.
4.If the test result is negative and clinical symptoms persist, additional testing using other clinical methods is recommended. A negative result does not at any time preclude the possibility of CMV infection.
LITERATURE REFERENCES
Cytomegalovirus(CMV) IgG/IgM Rapid Test
Cat. No.: RH0536X
SPECIMEN: Whole Blood/ Serum/ Plasma
INTENDED USE
The One Step CMV IgG/IgM Rapid Test Device is a rapid qualitative lateral flow test designed for the quantitive detection of IgG and IgM antibodies to Cytomegalovirus (CMV) in human Whole blood, serum or plasma samples.
INTRODUCTION
Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients.
PRINCIPLE
The One Step CMV IgG/IgM Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to CMV in Whole blood, Serum or Plasma. Each test consists of: 1) a burgundy colored conjugate pad containing CMV recombinant envelope antigens conjugated with Colloid gold (CMV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-CMV, T2 band is coated with antibody for the detection of IgG anti-CMV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-CMV, if present in the specimen, will bind to the CMV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a CMV IgG positive test result and suggesting a recent or repeat infection. IgM anti-CMV if present in the specimen will bind to the CMV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a CMV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.
KIT COMPONENTS
| Individually packed test devices | Each device contains a strip of CMV with colored conjugates and reactive reagents pre-spreaded at the corresponding regions. |
| Disposable pipettes | For adding specimens use. |
| Buffer | Phosphate buffered saline and preservative. |
| Package insert | For operation instruction. |
| Specimen collection container | For specimens collection use. |
| Timer | For timing use. |
| Centrifuge | For preparation of clear specimens |
PRECAUTIONS
STORAGE AND STABILITY
SPECIMEN COLLECTION AND STORAGE
PROCEDURE
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.
1.Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2.Place the test device on a clean and level surface.
3.Hold the dropper vertically and transfer 1 drop of Plasma/serum specimen (approximately 10μl) or 2 drops of whole blood specimen (approximately 20μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below.
4.Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Notes: Applying sufficient amount of specimen is essential for a valid test result. If migration (the wetting of membrane) is not observed in the test window after one minute, add one more drop of buffer to the specimen well.
INTERPRETATION OF RESULTS
POSITIVE RESULT : IgM Positive: * The colored line in the control line region (C) appears and a colored line appears in test line region1 (T1).The result indicates the presence of CMV specific IgM antibodies.
IgG Positive: * The colored line in the control line region (C) appears and a colored line appears in test line region 2 (T2). The result indicates the presence of CMV specific IgG antibodies.IgG and IgM Positive: * The colored line in the control line region (C) appears and two colored lines should appear in test line regions 1 and 2 (T1 and T2). The color intensities of the lines do not have to match. The result indicates that the presence of both CMV specific IgG and IgM antibodies.*NOTE: The intensity of the color in the test line region(s) (T1 and/or T2) will vary depending on the concentration of CMV antibodies in the specimen. Therefore, any shade of color in the test line region(s) (T1 and/or T2) should be considered positive.
NEGATIVE RESULT:
The colored line in the control line region (C) appears. No line appears in test line regions 1 or 2 (T1 or T2). Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.The colored line in the control line region (C) appears. No line appears in test line regions 1 or 2 (T1 or T2).QUALITY CONTROL
LIMITATIONS OF THE TEST
1.The One Step CMV IgG/IgM Rapid Test Device is for in vitro diagnostic use only. The test should be used for the detection of CMV antibodies in Whole Blood /Serum / Plasma specimens only. Neither the quantitative value nor the rate of increase in CMV antibodies can be determined by this qualitative test.
2.The One Step CMV IgG/IgM Rapid Test Device will only indicate the presence of CMV antibodies in the specimen and should not be used as the sole criteria for the diagnosis of CMV infection.
3.As with all diagnostic tests, all results must be interpreted together with other clinical information available to the physician.
4.If the test result is negative and clinical symptoms persist, additional testing using other clinical methods is recommended. A negative result does not at any time preclude the possibility of CMV infection.
LITERATURE REFERENCES
Span Biotech Ltd. is a research based company for rapid tests, with strong support from National Key Laboratory of Technology Projects of 10th and 11th Five-Year Plan and Faculty of Life Sciences of HuBei University. SpanBio also housed a R&D team that is developing gene recombination, cell cultivation and protein purification techniques. SpanBio pays strict attention on rapid tests for human being, animal diseases and food safety detection. It provides a number of customized services to professional distributors and partnering affiliates with excellent quality, competitive prices and super service.
Our mission:
Packaging Details:
Pouch+Box+Carton packaging
(1) With our company’s Logo
(2) With the natural package
(3) With OEM package
(4) ODM
Anna
Int'l Market Executive
SPANBIO
Tel: +86(755)89589611
Cell Phone:+8613417551798(WhatsApp)
EMAIL: anna.lee@spanbio.com
-
Span Biotech Ltd. is a research based company for rapid tests, with strong support from National Key Laboratory of Technology Projects of 10th and 11th Five-Year Plan and Faculty of Life Sciences of HuBei University. SpanBio also housed a R&D team that is developing gene recombination, cell cultivation and protein purification techniques. SpanBio pays strict attention on rapid tests for human being, animal diseases and food safety detection. It provides a number of customized services to professional distributors and partnering affiliates with excellent quality, competitive prices and super service.
Efficiently structured to provide lasting and economic health care solutions with export ready goods, our main products cover the following immunodiagnostic rapid test kits:
Rapid Tests for Human Use :
1) Fertility: Pregnancy HCG, ovulation LH, menopause FSH
2) Infectious diseases: Hepatitis B, HCV, HIV
3) Drug abuse: AMP, BAR, BZO, COC, mAMP, MOP, MTD, OPI, PCP, TCA, THC
4) Tumor markers: CEA, PSA, AFP, FOB
5) STDs(Sexually Transmitted Diseases): Gonorrhea, syphilis, chlamydia
6) New products: Malaria, H. Pylori, Multi-Hepatis B Panel (HBsAg, Anti-HBs, HBeAg, Anti-HBe, Anti-HBc), Blood Glucose Test, Multi-drug of Abuse Panel, Avian (Bird) Flu Rapid Test, etc.
Rapid Tests for Veterinary :
1) Bovine: Cow Pregnancy , Cow Ovulation, Bovine Brucella, Bovine Tuberculosis ,Food and Mouth Disease NSP Ab Test
2) Canine: Canine Distemper, Canine Parvovirus, Canine Coronavirus
3) Feline : Feline Leukemia Virus Ag Rapid Test ,Feline Panleucopenia Virus Ag Test,Feline Immunodeficiency Virus Ab Test
Rapid Tests for Food Safety :
1)For Antibiotics Residue : Nitrofurans (AOZ,AMOZ, AHD, SEM), Streptomycin , Sulfonamides , Chloramphenicol , Quinolone , Beta-Lactam&Tetracycline Combo (2 in 1), β-Lactams & Streptomycin & Chloramphenicol & Tetracyclines Combo (4 in 1), Beta-Lactam, Tetracycline test
2) For Beta-Agonist Residue : Ractopamine, Clenbuterol ,Salbutamol
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