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Legionella IgG/IgM/IgA ELISA 试剂盒

The Borrelia burgdorferi Legionella IgG/IgM/IgA ELISA Kit (ABIN997005) is a Colorimetric ELISA Kit designed to quantify Borrelia burgdorferi Legionella IgG/IgM/IgA.
产品编号 ABIN997005
发货至: 中国
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Quick Overview for Legionella IgG/IgM/IgA ELISA 试剂盒 (ABIN997005)

抗原

Legionella IgG/IgM/IgA

适用

Borrelia burgdorferi

检测方法

Colorimetric

实验类型

Competition ELISA

应用范围

ELISA
  • 原理

    Legionella IgG/IgM/IgA ELISA Test System is an enzyme-linked immunosorbent assay for the qualitative detection of total antibody (IgG/IgM/IgA) to Legionella pneumophila serogroups 1-6 in human sera.

    Analytical Method

    Qualitative

    特异性

    93.1%

    灵敏度

    92.3%
  • 样本量

    10 μL

    实验时间

    1 - 2 h

    板类型

    Pre-coated

    限制

    仅限研究用
  • 储存条件

    4 °C

    有效期

    12-18 months
  • 抗原

    Legionella IgG/IgM/IgA

    别名

    Legionella G/M/A

    物质类

    Antibody

    背景

    L. pneumophila was identified as the causative agent for Legionellosis (Legionella pneumonia, or Legionnaire's Disease) in 1977. Presently, there are more than 25 species and 33 serogroups in the family Legionellaceae, with at least 18 species associated with pneumonia, accounting for roughly 1-5% of all cases of pneumonia. L. pneumophila displays a multitude of morphologies including the bacillus, coccobacillus, and elongated fusiform. Although often difficult to perform, the Gram stain will be Gram-negative. The antibody response to L. pneumophila may be both specific and nonspecific, since the patient may have antibodies to similar antigens from other Gram-negative bacteria. Optimum times for specimen collection appear to be within the first week of illness, or as soon as possible after the onset (acute specimen), and at least 3 weeks after the onset (convalescent specimen). By the IFA method, a single result of 1:256 is considered presumptive evidence of legionella infection. Diagnostic titers have been reported to be absent in as many as 25% of patients, but the use of multiple Legionella species as the antigen source and a polyvalent conjugate directed against IgG, IgM, and IgA maximize the accuracy of serological procedures.
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