Technical Data
Chlamydia trachomatis (FITC)
Applications: Direct FA staining of target antigens in a permissive tissue culture system. Working dilution must be determined by the user for his or her application but a starting range of 1:10-1:50 is suggested. Acetone fixation of the antigen source is recommended prior to staining.

Titer is 1:1000-3000 by indirect immunofluorescence vs. all serovars (A-K, L1-L3).

Chlamydia is caused by the bacterium Chlamydia trachomatis. The intracytoplasmic inclusions caused by the bacterium are draped around the infected cells nucleus. Chlamydia has a genome size of approximately 500-1000 kilobases and contains both RNA and DNA. The organism is also extremely temperature sensitive and must be refrigerated at 4C as soon as a sample is obtained. Colonization of Chlamydia begins with attachment to sialic acid receptors on the eye, throat or genitalia. It persists at body sites that are inaccessible to phagocytes, T-cells, and B-cells. It also exists as 15 different serotypes. These serotypes cause four major diseases in humans: endemic trachoma (caused by serotypes A and C), sexually transmitted disease and inclusion conjunctivitis (caused by serotypes D and K), and lymphogranuloma venereum (caused by serotypes L1, L2, and L3). Studies reveal that Chlamydia, because of its cell wall, is able to inhibit phagolysosome fusion in phagocytes. The cell wall is proposed to be gram-negative in that it contains an outer lipopolysaccharide membrane, but it lacks peptidoglycan in its cell wall. This lack of peptidoglycan is shown by the inability to detect muramic acid and antibodies directed against it. It may, however, contain a carboxylated sugar other than muramic acid. The proposed structure consists of a major outer membrane protein cross-linked with disulfide bonds. It also contain cysteine-rich proteins (CRP) that may be the functional equivalent to peptidoglycan. This unique structure allows for intracellular division and extracellular survival (Hatch 1996).
-Kenneth Todar, University of Wisconsin-Madison
1ml4C (-20C Glycerol)Blue IceRabbit
L2 + other serovar groups
Purified IgG fraction covalently coupled with high purity Isomer I of fluorescein isothiocyanate. Care is taken to ensure complete removal of any free fluorescein from the final product.
Purified, Liquid, 0.01M PBS, pH 7.2 with 10mg/ml BSA, 0.1% sodium azide
Purified elementary bodies, disrupted. Crossreacts with Chlamydia psittacii and Chlamydia pneumoniae (TWAR). Negative vs. HEp-2 cells and egg yolk sac.
Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.