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digene HC2 CT-ID DNA Test

检测沙眼衣原体感染

S_1084_5_GEN_V2

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digene HC2 CT-ID DNA Test

Cat. No. / ID:   5135-1220

For 88 cervical samples (96 tests): CT Probe, Quality Controls, Calibrators, Capture Microplate, Reagents and Buffers
digene HC2 CT-ID DNA Test 旨在用于体外诊断用途。

✓ 全天候自动处理在线订单

✓ 博学专业的产品和技术支持

✓ 快速可靠的(再)订购

特点

  • 高度临床敏感度和特异性
  • 应用免疫检测进行信号扩增的核酸检测
  • 无需靶基因扩增,获得扩增的结果

产品详情

The digene HC2 CT-ID DNA Test is an in vitro microplate assay based on signal-amplified nucleic acid hybridization that uses chemiluminescence for the qualitative detection of Chlamydia trachomatis (CT) DNA from cervical specimens.

绩效

The digene HC2 CT-ID DNA Test provides high clinical sensitivity and specificity (see table).

High clinical sensitivity and specificity — CT testing
Method SensitivitySpecificity
Brush  97.7% 98.2%
Swab  92.3% 98.6%
The digene HC2 CT-ID DNA Test compared with culture and DFA.

原理

The digene HC2 CT-ID DNA Test is a nucleic acid hybridization assay with signal amplification that utilizes microplate chemiluminescent detection. Specimens containing the target DNA hybridize with a specific CT RNA probe cocktail. The resultant RNA–DNA hybrids are captured onto the surface of a microplate well that is coated with antibodies specific for RNA–DNA hybrids. Immobilized hybrids are then reacted with alkaline phosphatase-conjugated antibodies specific for RNA–DNA hybrids, and detected with a chemiluminescent substrate. Several alkaline phosphatase molecules are conjugated to each antibody. Multiple conjugated antibodies bind to each captured hybrid, resulting in substantial signal amplification. As the substrate is cleaved by the bound alkaline phosphatase, light is emitted, which is measured as relative light units (RLUs) on a luminometer. The intensity of the light emitted denotes the presence or absence of target DNA in the specimen.

程序

Cervical specimens are collected and transported using the digene HC2 DNA Collection Device or digene Female Swab Specimen Collection Kit. Specimens are denatured using a denaturation reagent and heat. The probe mix is added, and hybridization is carried out in a hybridization microplate. Hybridized samples are transferred to a capture microplate for hybrid capture. A detection reagent is added, and a wash step is carried out. A second detection reagent is added, and detection is carried out on a luminometer.

After denaturation, the procedure can be fully automated on the Rapid Capture System through to sample detection. Detection is then carried out manually on a luminometer.

Reimbursement

The digene HC2 CT-ID DNA Test is recognized by the American Medical Association (AMA) and reimbursed using "amplified probe technique" CPT codes (when appropriate).

应用

The digene HC2 CT-ID DNA Test is for qualitative detection of Chlamydia trachomatis (CT) in cervical specimens. The test can be used as a standalone test or as a follow-up test for detection of CT in specimens that were initially positive using the digene HC2 CT/GC DNA Test. The digene HC2 CT-ID DNA Test is indicated for use to identify symptomatic or asymptomatic women with Chlamydia trachomatis (CT) infection.

资源

试剂盒操作手册 (1)
安全数据表 (1)
Download Safety Data Sheets for QIAGEN product components.
Safety Data Sheets (1)
Certificates of Analysis (1)
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