Akzo Nobel N.v.

Roxanne Shurtliff

Joseph W Romano

Kimberly G Williams

Ranajit Pal

An isothermal transcription based amplification assay for the detection or quantification of chemokine RNA uses primers and probes for sequences within the gene for RANTES, MIP-1&agr; and MIP-1 &bgr;. The quantitative system uses an internal control Q of a mutant version of each gene. Target specific primers and probes are also disclosed.

Isothermal transcription based assay for the detection and quantification of chemokines rantes, MIP-1&agr; and MIP-1&bgr;

An isothermal transcription based amplification assay for the detection or quantification of chemokine RNA uses primers and probes for sequences within the gene for RANTES, MIP-l.alpha. and MIP-1 .beta.. The quantitative system uses an internal control Q of a mutant version of each gene. Target specific primers and probes are also disclosed.

Isothermal transcription based assay for the detection and

An isothermal transcription based amplification assay for MDC RNA uses primer combinations for sequences within the MDC gene. A quantitative control uses a mutant RNA for comparison.

Isothermal transcription based amplification assay for the detection and

An isothermal transcription based amplification assay for the detection of HTLV I RNA uses primers and probes for sequences within the tax gene, the pol gene, or the gag gene. An isothermal transcription based amplification assay for the detection of HTLV II uses primers and probes for sequences within the tax gene. Target specific primers and probes are also disclosed.

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Herndon, VA, United States of America

Roxanne Shurtliff