Catalogue number
Description
Features

Onar®Ls & Onar®Lp

Supplier: Minerva Biolabs

Onar® Lp-QP

Catalogue numberPack size
21-302525 tests
21-3100100 tests
21-3250250 tests

Onar® Ls

Catalogue numberPack size
21-102525 tests
21-1100100 tests
21-1250250 tests

Onar® Ls-QP

Catalogue numberPack size
21-202525 tests
21-2100100 tests
21-2250250 tests

Onar®Ls - Legionella species Diagnosis

Kit for in vitro diagnosis of Legionella species

and

Onar®Lp - Legionella pneumophila Diagnosis

kit for in vitro diagnosis of legionella pneumophila

The Onar® system is an in vitro test for the qualitative and quantitative diagnosis of Legionella species (Ls) or Legionella pneumophila (Lp) in clinical samples. The test is based on the polymerase chain reaction, and thus providing highly sensitive and approx. 100% specific rapid diagnosis. Onar® is CE-marked and approved for in vitro clinical diagnostics. The test system has undergone extensive internal validation, as well as external clinical evaluations. Onar®Ls is available as a conventional PCR assay with result evaluation by agarose gel, as well as a quantitative PCR probe system for use on most real-time instruments (Onar®Ls-QP and Onar®Lp-QP ).

Last modified: 2008-05-14 16:46:46
  • Highly sensitive Detection of fewer than 10 legionella particles per sample volume.
  • Highly specific for Legionella species: serogroups 1-14 and SG 16 of Legionella pneumophila, as well as other human pathogenic species of legionella like: L. longbeachae, L. dumoffii, L. bozemanii, L. gormanii, L. anisa, L. cherrii, L. parisiensis, L. tucsonensis, and L. wadsworthii or for Legionella pneumophila
  • Reliable The kit contains a positive control DNA, and a specific internal control probe for optional PCR quality check.
  • Ease of use Onar® allow convenient testing of clinical samples. The easy to follow step-by-step protocol does not require an experienced molecular biologist.
  • Convenient Reagents aliquoted for 25 reactions for convenient periodic or routine testing.
  • Validated Clinically and technically validated according to the European In Vitro Diagnostic Directive.
  • Results are easily determined
Last modified: 2008-05-14 16:46:46

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