Amplite® Tyramide (TSA) UV Channel Signal Scavenger *10X*
Tyramide signal amplification (TSA) is a technique used to enhance the signal of target molecules, such as antibodies or nucleic acid probes. This technique is particularly useful when working with samples that have low levels of target molecules or weak signals. TSA works by utilizing the enzymatic activity of horseradish peroxidase (HRP), which can catalyze the deposition of labeled tyramide molecules in close proximity to the target molecules. The tyramide molecules contain a reporter group, such as a fluorescent dye, which generates a detectable signal upon enzymatic reaction. This localized deposition of labeled tyramide molecules leads to signal amplification at the site of the target molecules, making them more easily detectable. Recently multicolor TSA detections are increasingly used for complicated detections, e.g., cancer diagnostics. There are a number of fluorescent tyramides available for TSA applications. However, some of the long wavelength tyramide conjugates tend to leak to UV (e.g., DAPI) and green (FITC) channel. This phenomenon is particularly severe with NIR or infrared tyramide or styramide conjugates. Amplite® Tyramide (TSA) UV Channel Signal Scavenger is used to quench the leaked fluorescence of UV (DAPI) and green (FITC) channel to eliminate or reduce the background resulted from the leakage of with NIR or infrared tyramide or styramide conjugates.
References
View all 5 references: Citation Explorer
Use of tyramide-fluorescence in situ hybridization and chromosome microdissection for ascertaining homology relationships and chromosome linkage group associations in oats.
Authors: Sanz, M J and Loarce, Y and Ferrer, E and Fominaya, A
Journal: Cytogenetic and genome research (2012): 145-56
Authors: Sanz, M J and Loarce, Y and Ferrer, E and Fominaya, A
Journal: Cytogenetic and genome research (2012): 145-56
Assignment of N-acetyl-D-glucosaminidase (Mgea5) to rat chromosome 1q5 by tyramide fluorescence in situ hybridization (T-FISH): synteny between rat, mouse and human with Insulin Degradation Enzyme (IDE).
Authors: Van Tine, B A and Patterson, A J and Kudlow, J E
Journal: Cytogenetic and genome research (2003): 202B
Authors: Van Tine, B A and Patterson, A J and Kudlow, J E
Journal: Cytogenetic and genome research (2003): 202B
Tissue distribution of products of the mouse decay-accelerating factor (DAF) genes. Exploitation of a Daf1 knock-out mouse and site-specific monoclonal antibodies.
Authors: Lin, F and Fukuoka, Y and Spicer, A and Ohta, R and Okada, N and Harris, C L and Emancipator, S N and Medof, M E
Journal: Immunology (2001): 215-25
Authors: Lin, F and Fukuoka, Y and Spicer, A and Ohta, R and Okada, N and Harris, C L and Emancipator, S N and Medof, M E
Journal: Immunology (2001): 215-25
Assignment of human MFNG, manic fringe Drosophila homolog, to 22q13.1 using tyramide fluorescence in situ hybridization (T-FISH).
Authors: Van Tine, B A and Knops, J and Shaw, G M and May, W A
Journal: Cytogenetics and cell genetics (1999): 132-3
Authors: Van Tine, B A and Knops, J and Shaw, G M and May, W A
Journal: Cytogenetics and cell genetics (1999): 132-3
Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique.
Authors: Van Tine, B A and Knops, J F and Butler, A and Deloukas, P and Shaw, G M and King, P H
Journal: Genomics (1998): 296-9
Authors: Van Tine, B A and Knops, J F and Butler, A and Deloukas, P and Shaw, G M and King, P H
Journal: Genomics (1998): 296-9
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