手机验证
大量
仅供科研使用
上海沪震实业有限公司
盒
Features & Benefits
Feature | Benefit |
---|---|
Small, self-contained hand-held cassette | No isolation room needed Convenient, easy-to-use, disposable device |
HDA technology | Rapid method of nucleic acid amplification that does not require thermal cycler |
Lyophilized Master Mix reagent | Easy-to-use format, just rehydrate with diluted sample. |
Small easy-to-use heat blocks | Eliminates need for dedicated molecular space and costly capital equipment. Allows for testing in smaller labs. |
CLIA moderately complex | Requires minimal training |
Refrigerated storage | No freezer needed. 2°C to 8°C storage. |
Long shelf life | 24 months from date of manufacture |
Room temperature set up | No ice or cooling block required |
Sample Type | Cutaneous and mucocutaneous lesion specimens from symptomatic patients |
Time to results | Approximately 60 minutes |
Reagent storage conditions | 2°C to 8°C Dilution and Reaction Tubes; 2°C to 30°C Amplicon Cartridge and Detection Cassette |
Controls storage conditions | 2°C to 8°C |
Sample preparation storage conditions | 20°C to 25°C for 1 hour prior to testing; 2°C to 8°C for 8 hours; and 1 month at –20°C to –70°C |
HSV-1 Sensitivity* | Cutaneous Lesions – 100% (95% CI 88.6% to 100%); Mucocutaneous Lesions – 94.9% (95% CI 90.3% to 97.4%) |
HSV-1 Specificity* | Cutaneous Lesions – 97.1% (95% CI 94.6% to 98.5%); Mucocutaneous Lesions – 96.5% (95% CI 94.8% to 97.7%) |
HSV-2 Sensitivity* | Cutaneous Lesions - 98.3% (95% CI 91.0% to 99.7%); Mucocutaneous Lesions - 97.4% (93.4% to 99.0%) |
HSV-2 Specificity* | Cutaneous Lesions: 95.6% (95% CI 92.8% to 97.3%); Mucocutaneous Lesions: 95.8% (94.2% to 97.0%) |
LOD* | HSV-1: 1.1 x 105 TCID50/mL; HSV-2: 1.1 x 104 TCID50/mL |
*Refer to Package Insert for additional performance claims.
Catalog Number | Description | Kit Size / Case Size |
---|---|---|
M210 | Assay Kit |
16 tests |
M109 | Quidel Molecular HSV 1+2 Control Set |
1 mL |
The AmpliVue HSV 1+2 Assay is an in vitro diagnostic test for the qualitative detection and differentiation of Herpes simplex virus type 1 (HSV-1) and Herpes simplex virus type 2 (HSV-2) nucleic acids isolated from cutaneous and mucocutaneous lesions of symptomatic patients.
The assay consists of three major steps: (1) specimen preparation (one-step dilution), (2) isothermal Helicase-Dependent Amplification (HDA) of target amplicons specific to HSV-1 and HSV-2, and (3) detection of the amplified DNA by target-specific hybridization probes via a colorimetric reaction on a lateral-flow strip which is embedded in a self-contained disposable cassette to prevent amplicon contamination.
Specimen preparation involves a simple one step dilution in which specimens in viral transport medium are added to a dilution tube. The diluted sample is transferred into Reaction Tube containing lyophilized mix of HDA reagents including primers specific for the amplification of HSV-1 and HSV-2. Competitive amplification of the process control DNA takes place unless amplification inhibitory substances are present or the sample processing fails.
After completion of the HDA reaction, the Reaction Tube is transferred to a Cassette for rapid detection with the test result displayed as test and/or control lines in the window of the Cassette. The dual-labeled probe-amplicon hybrid is then detected by the lateral flow strip within the Cassette. The HSV-1 amplicon is captured at the T1-Line and HSV-2 amplicon is captured at the T2-Line, while the process control amplicon is captured at the C-Line. The Biotin in the amplicon-probe complexes captures the streptavidin-conjugated color particles for visualization and the molecular test result is shown as colored lines that are visually read.
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