Image may differ
AESKULISA®
Reference:
6012
Designation:
Toxoplasma gondii IgG
Intended use:

The AESKULISA® Toxoplasma gondii IgG and IgM tests are qualitative and quantitative immunoassays for the detection of human IgG and IgM antibodies in serum or plasma against Toxoplasma gondii. The AESKULISA® Toxoplasma gondii IgM serves as an initial test for the detection of acute infections. The AESKULISA® Toxoplasma gondii IgG allows the confirmation of pathogen contact and supports the determination of the immune status. The results can only be interpreted in conjunction with the clinical picture. A diagnosis should not be based solely on the results of the test performed, but should always be made taking into account all clinical and laboratory findings. Further tests should be carried out for confirmation. AESKULISA® immunoassays are suitable for use by healthcare professionals with appropriate professional training in the use of in vitro diagnostics.

Method:
ELISA
Conjugate:
IgG
Analysis:
Qualitative
,
Quantitative
Cut Off:
Cut-off control
Measurement range:
Kit-specific
QC certificate
Calibration:
13/132
,
WHO
Provisions:
1 x 96
Kit-Configuration:
Single
Number of antigens:
1
Registration:
CE marking
Coated Antigens:
Specific cell wall material of Toxoplasma gondii
strain RH
AESKULISA®

6012

Toxoplasma gondii IgG

Image may differ
Intended use:

The AESKULISA® Toxoplasma gondii IgG and IgM tests are qualitative and quantitative immunoassays for the detection of human IgG and IgM antibodies in serum or plasma against Toxoplasma gondii. The AESKULISA® Toxoplasma gondii IgM serves as an initial test for the detection of acute infections. The AESKULISA® Toxoplasma gondii IgG allows the confirmation of pathogen contact and supports the determination of the immune status. The results can only be interpreted in conjunction with the clinical picture. A diagnosis should not be based solely on the results of the test performed, but should always be made taking into account all clinical and laboratory findings. Further tests should be carried out for confirmation. AESKULISA® immunoassays are suitable for use by healthcare professionals with appropriate professional training in the use of in vitro diagnostics.

Method:
ELISA
Conjugate:
IgG
Analysis:
Qualitative
,
Quantitative
Cut Off:
Cut-off control
Measurement range:
Kit-specific
QC certificate
Calibration:
13/132
,
WHO
Provisions:
1 x 96
Kit-Configuration:
Single
Number of antigens:
1
Registration:
CE marking
Coated Antigens:
Specific cell wall material of Toxoplasma gondii
strain RH
Downloads
All related documents and information clearly summarized

Instructions for Use

Safety Data Sheet