SeroCP RT C. pneumoniae IgG ELISA Assay

$435.00

The SeroCP IgG (RT) ELISA Assay kit is intended for the detection of IgG antibodies specific to Chlamydia pneumoniae in human serum. The SeroCP IgG (RT) kit is a qualitative Enzyme Linked Immunosorbent Assay (ELISA) which is used as an aid in the diagnosis of Chlamydia pneumoniae infection. Savyon SeroCP IgG (RT) is a new configuration of ELISA test which presents advantageous features: incubations at ambient temperature; short test duration; and utilizing ready-to-use conjugate. The Eagle Biosciences SeroCP IgG (RT) ELISA Assay Kit is for Research Use Only and is not intended for diagnostic or therapeutic purposes.

SKU: 1191-01 Categories: , ,

SeroCP RT C. pneumoniae IgG ELISA Assay

The SeroCP RT C. pneumoniae IgG ELISA Assay is For Research Use Only

Size: 1×96 wells
Sensitivity: Cut-Off Control
Incubation Time: 1.5 hours
Sample Type: Serum
Sample Size: 10 µl


Assay Principle

The Eagle Biosciences SeroCP RT Plates are coated with C. pneumoniae specific antigens. Serum to be tested is diluted and incubated with the pre-coated SeroCPTM RT plate 30 minutes at Room Temperature (RT).  In this step C. pneumoniae specific antibodies are bound to the immobilized C. pneumoniae specific antigens. Non-specific antibodies are removed by washing. Anti-human IgG conjugated to horseradish peroxidase (HRP) is added and incubated 30 minutes at Room Temperature. In this step the HRP-conjugate is bound to the pre-formed antigen-antibody complex. Unbound conjugate is removed by washing. Upon the addition of TMB substrate, the substrate is hydrolyzed by the peroxidase, yielding a blue solution of the reduced substrate. Upon the addition of the stop solution, the blue color turns yellow and should be read by an ELISA reader at a wavelength of 450/620 nm. The absorbance is proportional to the amount of the specific antibodies which are bound to the immobilized C. pneumoniae specific antigens.


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SeroCP Quant C. pneumoniae IgG ELISA Assay Kit
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Additional Information

Assay Background


Chlamydia pneumoniae (TWAR183) is an emerging infectious agent with a spectrum of clinical manifestations, including upper and lower respiratory tract infections. The majority of C. pneumoniae infections are mild and asymptomatic yet, may cause serious diseases, such as pharyngtitis, sinusitis, acute bronchitis and community acquired pneumonia. Undetected and untreated infection may lead to prolonged and persistent disease. Recent data indicates a possible association between C. pneumoniae infection and chronic diseases. Seroprevalence of C. pneumoniae among children is low but increases sharply until middle age, where after it remains high. Difficulties in sample collection and inaccessibility of the infected site seriously affect the usefulness of direct detection methods. Therefore, serological testing is routinely used and serves as a non-invasive tool in identification of both distal and chronic chlamydial infections, where direct detection methods are rarely efficient. In addition, the presence of certain antibody types may also indicate the state of the disease.

Primary chlamydial infection is characterized by a predominant IgM response within 2 to 4 weeks and a delayed IgG and IgA response within 6 to 8 weeks. After acute C. pneumoniae infection, IgM antibodies are usually lost within 2 to 6 months, IgG antibody titers usually decrease slowly; whereas IgA antibodies tend to disappear rapidly. When primary chlamydial infection is suspected, the detection of IgM is highly diagnostic. However, in recurrent or chronic infections the prevalence of IgM is low and therefore absence of IgM does not necessarily exclude on-going infection. In reinfection, IgG and IgA levels rise quickly, often in one to two weeks. IgA antibodies have shown to be a reliable immunological marker of primary, chronic and recurrent infections. These antibodies usually decline rapidly to baseline levels following treatment and eradication of the chlamydia infections. The persistence of elevated IgA antibody titers is generally considered as a sign of chronic infection.

IgG antibodies persist for long periods and decline very slowly. Therefore, the presence of IgG antibodies is mainly indicative of a chlamydia infection at an undetermined time. However, a four-fold rise in IgG or high levels of IgG antibodies may indicate an on-going chronic infection. The SeroCP RT is an ELISA based assay in which purified elementary bodies of C. pneumonaie (TWAR-183) are used as antigens to detect the antibody response in humans. For complete diagnosis of current, chronic or past infections, it is recommended to determine IgG, IgM and IgA antibodies to C. pneumoniae.

References


  1. Myhra, W., Mordhors, C.H., Wang, S.P., Grayston, J.T., (1990). Clinical features of Chlamydia pneumoniae, strain TWAR, infection in Denmark 1975-1987.
  2. Bowie WR, Caldwell HD, Jones RP, et al., eds. Chlamydial infections. Cambridge, UK: Cambridge University Press, 422-425.
  3. Saikku, P., Leinonen, M., Tenkanen, L., Linnanmaki, E., Ekman, M.R., Manninen, V., Manttari, M., Frick, M.H. and Huttunen, J.K. (1992). Chronic Chlamydia pneumoniae infection as a risk factor for coronary heart disease in the Helsinki heart study. Ann. Intern. Med. 116: 273-278.
  4. Sarov, I., Kleinman, D., Cevenini, R., Hocberg, G., Potashnik, G., Sarov, B. and Insler, V. (1986). Specific IgG and IgA antibodies to Chlamydia trachomatis in infertile women. In. J. Fertil. 31 (3): 193-197.
  5. Campbell, L.A. (1993). PCR detection of Chlamydia pneumoniae In Diagnostic Molecular Microbiology: Principles and Applications (Persing, D.H., Smith, T.F., Tenover, F.C. and White, T.J., Eds). ASM Press. pp. 247-252
  6. Henry-Suchet, J., Askienazy-Elbhar, M., Thibon, M., Revol, C. and Akue, B.A. (1994).Post-therapeutic evolution of serum chlamydia antibody titers in women with acute salpingitis and tubal infertility. Fertility and Sterility. 62: No. 3.
  7. Saikku, P., Matila, K., Nieminen, M.S., Huttunen, J.K., Leinon, M., Eckman, M.R., Makela, P.H. and Valtonen, V. (1988). Serological Evidence of an Association of aNovel Chlamydia TWAR with Chronic Coronary Heart Disease and Acute Myocardial Infarction. Lancet. 2: 983-986.
  8. Grayston, J.T., Cambell, L.A., Mordhorst, C.H., Saikku, P., Thom, D. and Wang, S.P.(1989). A New Respiratory Pathogen: Chlamydia pneumoniae Strain TWAR. J. Inf.Dis. 161: 618-625.
  9. Saikku, P., Leinonen, M., Tenkanen, L., Linnanmaki, E., Ekman, M.R., Mannin, V., Manttari, M., Frick, M.H. and Huttunen, J.K. (1992). Chronic Chlamydia pneumoniae Infections as a Risk Factor for Coronary Heart Disease in the Helsinki Heart Study Ann. of Int. Med. 116: 273-278.

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