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Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections
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Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections
ABBOTT MOLECULAR INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
09N17-03A | 0 | - | ||
09N17-03B | 0 | - | ||
09N17-085 | 0 | - | ||
09N18-001 | 0 | - | ||
09N19-012 | 0 | - | ||
09N20-002 | 0 | - | ||
09N20-012 | 0 | - |
BECTON, DICKINSON AND COMPANY | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
443979 | 0 | - | ||
443989 | 0 | - |
HOLOGIC LTD. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
ASY-09407 | 0 | - | ||
ASY-09408 | 0 | - | ||
PRD-03393 | 0 | - | ||
PRD-03837 | 0 | - |
Hologic, Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
301110 | 0 | - | ||
302931 | 0 | - | ||
302939 | 0 | - | ||
ASY-13822 | 0 | - | ||
ASY-13823 | 0 | - | ||
ASY-13954 | 0 | - | ||
ASY-13955 | 0 | - | ||
PRD-07039 | 0 | - | ||
PRD-07039 | 0 | - | ||
PRD-07040 | 0 | - | ||
PRD-07040 | 0 | - | ||
PRD-07041 | 0 | - | ||
PRD-07041 | 0 | - |
26 Results
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Catalog #
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Name
Company Name
Description
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Aptima Combo 2®
Hologic, Inc.
Aptima Combo 2® Assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) fromChlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal disease using the Panther® system as specified.
0
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Aptima Combo 2®
Hologic, Inc.
Aptima Combo 2® assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal disease using the Panther® system as specified.
0
-
Aptima Combo 2®
Hologic, Inc.
Aptima Combo 2® Assay, 250 test, box 2 of 2 (15°C to 30°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal urogenital disease.
0
-
Aptima Combo 2®
Hologic, Inc.
Aptima Combo 2® Assay, 250 test, box 1 of 2 (2°C to 8°C box). The Aptima Combo 2® assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal urogenital disease.
0
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Aptima®
HOLOGIC LTD.
Aptima® Mycoplasma genitalium Assay, 100 test, box 2 of 2 (15°C to 30°C box).
0
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Aptima®
HOLOGIC LTD.
Aptima® Mycoplasma genitalium Assay, 100 test, box 1 of 2 (2°C to 8°C box).
0
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Aptima®
Hologic, Inc.
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.
0
-
Aptima Combo 2®
Hologic, Inc.
Aptima Combo 2® Assay, 100 test, box 1 of 2 (2°C to 8°C box). The Aptima Combo 2® Assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal disease using the Panther® System as specified.
0
-
Aptima Combo 2®
Hologic, Inc.
Aptima Combo 2® Assay, 100 test, box 2 of 2 (15°C to 30°C box). The Aptima Combo 2® Assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) to aid in the diagnosis of chlamydial and/or gonococcal disease using the Panther® System as specified.