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The ELISA analytical biochemical technique of the MBS016993 kit is based on TRAP antibody-TRAP antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TRAP antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, TRAP.
The kit is approved for human In Vitro Diagnostic Use and was primarily intended for detecting TRAP positive cells in peripheral blood or bone marrow, particularly for the detection of TRAP positive cells associated with Hairy Cell Leukemia.
The TRAPeze® Telomerase Detection Kit is a highly sensitive in vitro assay system for detecting telomerase activity. The assay is a one-buffer, two-enzyme, system utilizing PCR to enhance the sensitivity of telomerase detection in small samples.
The TRAPEZE® XL Kit is a highly sensitive in vitro assay for the fluorometric detection of telomerase activity. It incorporates refinements to the original TRAP assay that were first introduced in the gel-based TRAPEZE® Telomerase Detection Kit (Cat #S7700).
TRAP assay is a popular method to determine telomerase activity. It includes extension, amplification, and detection of telomerase products. This technique is crucial for studying telomerase activity in various cells, tissues, and specimens, especially in the context of cancer research and aging.
perform the Telomeric Repeat Amplification Protocol (TRAP) and ELISA assay for non-quantitative detection of telomerase activity in cells and tissues. The novice user is advised to read the entire manual prior to using the
20 lis 2015 · In this detailed protocol we describe Telomere Repeat Amplification Protocol (TRAP). The TRAP assay is a popular method to determine telomerase activity in mammalian cells and tissue samples (Kim et al., 1994). The TRAP assay includes three steps: extension, amplification, and detection of telomerase products.
