Hologic, Inc.
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Hologic, Inc.
| Hologic | ||||
| CATALOG # | QTY | PRICE | DESCRIPTION | |
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718 Results
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Aptima®
Hologic
Aptima® General Purpose Reagents, 250 test, box 2 of 2 (2°C to 8°C box). The Aptima® General Purpose Reagents (GPRs) feature Transcription-Mediated Amplification (TMA®) and Hybridization Protection Assay (HPA) technologies. Aptima® GPRs may be used to facilitate the development of tests by CLIA-certified high complexity laboratories or research laboratories for the qualitative detection of nucleic acid-based analytes.
0
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Aptima®
Hologic
Aptima® General Purpose Reagents, 250 test, box 1 of 2 (15°C to 30°C box). The Aptima® General Purpose Reagents (GPRs) feature Transcription-Mediated Amplification (TMA®) and Hybridization Protection Assay (HPA) technologies. Aptima® GPRs may be used to facilitate the development of tests by CLIA-certified high complexity laboratories or research laboratories for the qualitative detection of nucleic acid-based analytes.
0
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Aptima®
Hologic
Aptima® GC assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima® Neisseria gonorrhoeae assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection of ribosomal RNA (rRNA) from Neisseria gonorrhoeae (GC) to aid in the diagnosis of gonococcal urogenital disease using the Tigris® DTS® System or semi-automated instrumentation as specified.
0
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Aptima®
Hologic
Aptima® GC assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima® Neisseria gonorrhoeae assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection of ribosomal RNA (rRNA) from Neisseria gonorrhoeae (GC) to aid in the diagnosis of gonococcal urogenital disease using the Tigris® DTS® System or semi-automated instrumentation as specified.
0
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Aptima®
Hologic
The Aptima® Controls Kit is for use with the Aptima® Assays for the detection of C. trachomatis and/or N. gonorrhoeae. These quality control reagents are to be used according to the instructions in the package insert of the appropriate Aptima® Assay to establish run validity.
