Dna-Reagents, Neisseria
Main Filters
Dna-Reagents, Neisseria
ABBOTT MOLECULAR INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
09N18-001 | 0 | - | ||
09N19-012 | 0 | - | ||
09N20-002 | 0 | - | ||
09N20-012 | 0 | - | ||
9K12-04 | 0 | - |
BECTON, DICKINSON AND COMPANY | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
440452 | 0 | - | ||
440928 | 0 | - | ||
441129 | 0 | - | ||
441354 | 0 | - | ||
441357 | 0 | - | ||
441358 | 0 | - | ||
441361 | 0 | - | ||
441362 | 0 | - | ||
441444 | 0 | - | ||
443376 | 0 | - | ||
443420 | 0 | - |
CEPHEID | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
GXCT/NG-10 | 0 | - | ||
GXCT/NG-120 | 0 | - |
Hologic, Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
102830 | 0 | - | ||
105575 | 0 | - | ||
301048 | 0 | - | ||
301072-01 | 0 | - | ||
301073-02 | 0 | - | ||
301092 | 0 | - | ||
301093 | 0 | - | ||
301110 | 0 | - | ||
301162 | 0 | - | ||
302002C | 0 | - | ||
302070 | 0 | - | ||
302071 | 0 | - | ||
302305 | 0 | - | ||
302307 | 0 | - | ||
302380 | 0 | - | ||
302382 | 0 | - | ||
302931 | 0 | - | ||
302935 | 0 | - | ||
302939 | 0 | - | ||
302943 | 0 | - | ||
303013 | 0 | - | ||
303014 | 0 | - | ||
902615 | 0 | - | ||
ASY-13822 | 0 | - | ||
ASY-13823 | 0 | - | ||
ASY-13954 | 0 | - | ||
ASY-13955 | 0 | - | ||
PRD-07039 | 0 | - | ||
PRD-07039 | 0 | - |
QIAGEN SCIENCES INC. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
5130-1220 | 0 | - | ||
5140-1220 | 0 | - |
Roche Molecular Systems, Inc. | ||||
CATALOG # | QTY | PRICE | DESCRIPTION | |
05200881001 | 0 | - |
108 Results
Results Per Page
- 50
- 100
- 250
Catalog #
AvailableQty
Starting At
Name
Company Name
Description
0
-
BD MAX™ UVE Sample Buffer Tubes
BECTON, DICKINSON AND COMPANY
BD MAX ™ UVE Sample Buffer Tubes Contains: 48 x 1.5 mL Sample Buffer Tubes
0
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BD MAX™ UVE Specimen Collection Kit
BECTON, DICKINSON AND COMPANY
BD MAX UVE Specimen Collection Kit
0
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Dilution Tubes (LBC) for the BD ProbeTec™ Qx Amplified DNA Assays
BECTON, DICKINSON AND COMPANY
Tube LBC Diluent Qx
0
-
Urine Preservative Transport for the BD ProbeTec™ Qx Amplified DNA Assays
BECTON, DICKINSON AND COMPANY
Urine Preservative Transport for the BD ProbeTec™ Qx Amplified DNA Assays
0
-
BD Swab Diluent for the BD ProbeTec™ QX Amplified DNA Assays
BECTON, DICKINSON AND COMPANY
Swab Diluent for the BD ProbeTec™ QX Amplified DNA Assays
0
-
Male Urethral Collection Kit for BD ProbeTec™ (CT/GC) Qx Amplified DNA Assays
BECTON, DICKINSON AND COMPANY
Swab Male Urethral Specimen Collection
0
-
BD ProbeTec™ Qx Collection Kit for Endocervical or Lesion Specimens
BECTON, DICKINSON AND COMPANY
BD ProbeTec™ Qx Collection Kit for Endocervical or Lesion Specimens Contains: 100 each sterile polyester-tipped cleaning swab, sterile polyurethane-tipped collection swab, Q? Swab Diluent tube
0
-
BD ProbeTec™ Urine Preservative Transport
BECTON, DICKINSON AND COMPANY
Tube Urine Preservation Transport
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) 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
-
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
-
Aptima®
Hologic, Inc.
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
-
Aptima®
Hologic, Inc.
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
-
Aptima®
Hologic, Inc.
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
-
Aptima®
Hologic, Inc.
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
-
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.
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 using the Tigris® DTS® Automated Analyzer or semi-automated instrumentation 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 using the Tigris® DTS® Automated Analyzer or semi-automated instrumentation as specified.
0
-
Aptima®
Hologic, Inc.
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
-
Aptima®
Hologic, Inc.
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
-
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 urogenital disease using the Tigris® DTS® Automated Analyzer or semi-automated instrumentation 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 urogenital disease using the Tigris® DTS® Automated Analyzer or semi-automated instrumentation as specified.
0
-
Aptima®
Hologic, Inc.
The Aptima® System Fluid Preservative Kit is used with the Aptima® Assays on the Tigris® DTS® System. Use the System Fluid Preservative Kit according to the instructions outlined in the appropriate assay package insert and the Tigris® DTS® System Operator’s Manual.
0
-
Aptima®
Hologic, Inc.
The Aptima® Auto Detect Kit. This kit is to be used with the Leader® HC+ Luminometer and the Tigris® instrument system.
0
-
Aptima®
Hologic, Inc.
The Aptima® Assay Fluids Kit is used with the Aptima® Assays on the Tigris® DTS® System. Use the Assay Fluids Kit according to the instructions outlined in the appropriate assay package insert and the Tigris® DTS® System Operator’s Manual.