Produit
CAT:
CRG1082-01
Taille:
10 μl
Prix:
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Qty:
Disponibilité et expédition
- Articles en stock livrables sous 24 à 48 heures et articles hors stock livrables sous 2 à 6 semaines
- Glace carbonique: Non requis
Description du produit
Cy3 labled Tyramide for Multiplex IHC staining or enhanced fluorescent IHC staining
Propriétés du produit
Dangereuxnon
Glace carbonique requisenon
Marque déposéenon
Informations complémentaires
Applications: MIHC, IF
Form: Liquid in PBS
Conditions de stockage: Store at 4 °C in dark for 1 year, do not freeze.
Notes: For multiplex immunohistochemical (mIHC) applications, the traditional enzymatic amplification procedures are sufficient for achieving adequate antigen detection. However, several factors limit the sensitivity and utility of these procedures. Tyramide signal amplification (TSA) has proven to be a particularly versatile and powerful enzyme amplification technique with improved assay sensitivity. TSA is based on the ability of HRP, in the presence of low concentrations of hydrogen peroxide, to convert labeled tyramine-containing substrate into an oxidized, highly reactive free radical that can covalently bind to tyrosine residues at or near the HRP. To achieve maximal IHC detection, tyramine is prelabeled with a fluorophore. The signal amplification conferred by the turnover of multiple tyramide substrates per peroxidase label translates ultrasensitive detection of low-abundance targets and the use of smaller amounts of antibodies and hybridization probes. In immunohistochemical applications, sensitivity enhancements derived from TSA method allow primary antibody dilutions to be increased to reduce nonspecific background signals, and can overcome weak immunolabeling caused by suboptimal fixation procedures or low levels of target expression.
Platform: Ex/Em = 553/569 nm
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