Fluorescent in situ hybridization Reagents
Apexbio Technology LLC Fluorescein TSA Fluorescence System Kit, 200-600 slides
Tyramine Signal Amplification (TSA) from APExBIO technology increases sensitivity by a factor of 100 and enables detection of low-abundance targets in fluorescent immunocytochemistry (ICC), immunohistochemistry (IHC) and in situ hybridization (FISH) applications. The TSA Fluorescence Kit uses horseradish peroxidase (HRP) to directly catalyze the covalent deposition of the fluorophore adjacent to the immobilized enzyme. The labeling process is so fast (less than ten minutes) and the deposition label can be viewed directly under standard or confocal microscopy. TSA fluorescein can also be used in combination with anti-fluorescein. TSA technology is used for bright field microscopy of enzyme conjugates and suitable chromogenic substrates. Other sizes are also available. Please inqury us for quote.
Genscript Corporation FGFR1 alpha IIIcBiotin Hi
Fibroblast growth factors (FGFs) comprise a family of at least eighteen structurally related proteins that are involved in a multitude of physiological and pathological cellular processes including cell growth differentiation angiogenesis wound healing and tumorgenesis The biological activities of the FGFs are mediated by a family of type I transmembrane tyrosine kinases which undergo dimerization and autophosphorylation after ligand binding FGFR1 is tyrosine-protein kinase that acts as cell-surface receptor for fibroblast growth factors and plays an essential role in the regulation of embryonic development cell proliferation differentiation and migration Required for normal mesoderm patterning and correct axial organization during embryonic development normal skeletogenesis and normal development of the gonadotropin-releasing hormone (GnRH) neuronal system
Enzo Life Sciences DIGX HPV type 16 18 probe (1ml)
The DIGX HPV type 16/18 probe is a mixture of digoxigenin-labeled HPV type 16 and HPV type 18 specific probes in buffered formamide and hybridization enhancers. Long Term Storage: +4°C.
Apexbio Technology LLC Cy3 TSA Fluorescence System Kit, 100-300 slides
Tyramine Signal Amplification (TSA) from APExBIO technology increases sensitivity by a factor of 100 and enables detection of low-abundance targets in fluorescent immunocytochemistry (ICC), immunohistochemistry (IHC) and in situ hybridization (FISH) applications. The TSA Fluorescence Kit uses horseradish peroxidase (HRP) to directly catalyze the covalent deposition of the fluorophore adjacent to the immobilized enzyme. The labeling process is so fast (less than ten minutes) and the deposition label can be viewed directly under standard or confocal microscopy. TSA fluorescein can also be used in combination with anti-fluorescein. TSA technology is used for bright field microscopy of enzyme conjugates and suitable chromogenic substrates. The use of TSA reagents results in a significant increase in sensitivity compared to standard assays while maintaining stable specificity and resolution. Other sizes are also available. Please inqury us for quote.
Apexbio Technology LLC Fluorescein TSA Fluorescence System Kit, 100-300 slides
Tyramine Signal Amplification (TSA) from APExBIO technology increases sensitivity by a factor of 100 and enables detection of low-abundance targets in fluorescent immunocytochemistry (ICC), immunohistochemistry (IHC) and in situ hybridization (FISH) applications. The TSA Fluorescence Kit uses horseradish peroxidase (HRP) to directly catalyze the covalent deposition of the fluorophore adjacent to the immobilized enzyme. The labeling process is so fast (less than ten minutes) and the deposition label can be viewed directly under standard or confocal microscopy. TSA fluorescein can also be used in combination with anti-fluorescein. TSA technology is used for bright field microscopy of enzyme conjugates and suitable chromogenic substrates. Other sizes are also available. Please inqury us for quote.
Apexbio Technology LLC Cy5 TSA Fluorescence System Kit, 200-600 slides
Tyramine Signal Amplification (TSA) from APExBIO technology increases sensitivity by a factor of 100 and enables detection of low-abundance targets in fluorescent immunocytochemistry (ICC), immunohistochemistry (IHC) and in situ hybridization (FISH) applications. The TSA Fluorescence Kit uses horseradish peroxidase (HRP) to directly catalyze the covalent deposition of the fluorophore adjacent to the immobilized enzyme. The labeling process is so fast (less than ten minutes) and the deposition label can be viewed directly under standard or confocal microscopy. TSA fluorescein can also be used in combination with anti-fluorescein. TSA technology is used for bright field microscopy of enzyme conjugates and suitable chromogenic substrates. The use of TSA reagents results in a significant increase in sensitivity compared to standard assays while maintaining stable specificity and resolution. Other sizes are also available. Please inqury us for quote.
Advanced Cell Diagnostics RNAscope 2.5 LS Probe - HPV16, Chromogenic detection, FFPE tissues, Single-molecule sensitivity, 1-20 copies per cell
RNAscope 2.5 LS Probe - HPV16, Chromogenic detection, FFPE tissues, Single-molecule sensitivity, 1-20 copies per cell
American Research Products Inc Anti CD136 MST1R Aveo anti RON
Anti-Human CD136/MST1R Antibody (Aveo anti-RON) Research Grade
Apexbio Technology LLC HyperScribe™ T7 High Yield Fluorescein RNA Labeling Kit, 25 rxns
HyperScribe™ T7 High Yield Fluorescein RNA Labeling Kit is designed to generate randomly fluorescein-modified RNA probes by in vitro transcription. Such probes are ideally suited for in situ hybridization and Northern blot hybridization experiments. The principle of labeling is similar to the basic labeling principle of a mixture of fluorescein RNA labels. Fluorescein-12-UTP is efficiently incorporated into RNA using the optimized reaction buffer and T7 RNA polymerase mixture in place of its natural counterpart UTP. An appropriate Fluorescein-12-UTP substitution typically achieves an optimal balance between reaction and labeling efficiency. However, the individual optimization of the Fluorescein-12-UTP / UTP ratio can be easily achieved using a single nucleotide format. The resulting fluorescein-modified RNA probe can then be detected by fluorescence spectroscopy Other sizes are also available. Please inqury us for quote.