Chlamydia pneumoniae IgM Control Serum (C1371M)

Host Quantity Applications Species Reactivity Data Sheet  
3 mL ELISA Chlamydia pneumoniae
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Overview
Product Name Chlamydia pneumoniae IgM Control Serum (C1371M)
Description Chlamydia pneumoniae IgM Control Serum (C1371M) are positive controls for immunoassays of the SERION ELISA classic product line and are obtained from the material of individual human donors.

Product is intended for research use.
Target Human Chlamydia pneumoniae IgM
Species Reactivity Chlamydia pneumoniae
Assay Type Any Immunoassay
Applications ELISA
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Chlamydia trachomatis IgM Control Serum (C1372M)
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Chlamydia pneumoniae COMC Antigen (Chlamydia Outer Membrane Complexes) Antigen (BA1371VS)
Chlamydia pneumoniae COMC Antigen (Chlamydia Outer Membrane Complexes) Antigen (BA1371VS)
Chlamydia trachomatis EB + RB Antigen (BA1372VSER)
Chlamydia trachomatis MOMP Antigen (BA1372VSR2)
Chlamydia abortus EB & RB (elementary and reticular bodies) Antigen (BA1373VSER)
Properties
Form Liquid
Background Ready-to-use positive controls for the qualitative and quantitative antigen determination when using immunoassays of the SERION ELISA classic,SERION ELISA antigen and SERION ELISA agile product line in accordance with modern quality guidelines. In addition to the controls contained in the SERION ELISA test kit, the ready-to-use components are an additional, external reagent for checking the validity of the test run carried out, for determining the laboratory-internal error limits and for documenting the batch-to-batch consistency of the method used. As part of extensive validation studies, target values ​​and areas of validity are determined for each test-specific SERION ELISA control and documented on batch-specific certificates of analysis. These serve as guide values, particularly within the framework of internal laboratory quality assurance in accredited testing laboratories in accordance with the guidelines of the German Medical Association (RiLiBÄK).
Specificity Information
Target ID Human Chlamydia pneumoniae IgM
Research Areas Infectious Disease
Application Images
Additional Information
Additional Information As part of extensive validation studies, target values ​​and areas of validity are determined for each test-specific SERION ELISA control and documented on batch-specific certificates of analysis. These serve as guide values, particularly within the framework of internal laboratory quality assurance in accredited testing laboratories in accordance with the guidelines of the German Medical Association (RiLiBÄK).
Handling
Storage Store at 2-8°C.
Application Instructions SERION ELISA control are ready to use and do not need to be further diluted. An Rf absorption for the determination of IgM antibodies is also not necessary.
References & Data Sheet