42250
Streptavidin-R-Phycoerythrin
≥1 mg/mL (active substance)
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form
liquid
Quality Level
concentration
≥1 mg/mL (active substance)
fluorescence
λex 566 nm; λem 576 nm in 0.1 M phosphate pH 7.0
storage temp.
2-8°C
1 of 4
This Item | 189732 | 11089153001 | GEPA45001 |
|---|---|---|---|
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level - |
| form liquid | form liquid | form liquid | form solid |
| concentration ≥1 mg/mL (active substance) | concentration - | concentration - | concentration - |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. -10 to -25°C | storage temp. 2-8°C |
| fluorescence λex 566 nm; λem 576 nm in 0.1 M phosphate pH 7.0 | fluorescence - | fluorescence - | fluorescence - |
General description
Streptavidin-R-Phycoerythrin is a fluorescent labeling agent comprised of a biotin-binding protein (streptavidin) covalently attached to a fluorescent label ((R-phycoerythrin). Streptavidin-R-phycoerythrin complexes provide the measurement method for the target phosphoprotein.[1] And, Streptavidin R-phycoerythrin extends the light tolerance of certain phycobiliproteins.[2]
Application
Streptavidin-R-Phycoerythrin (R-PE) is used to label biotin-conjugated (biotinylated) molecules and biotin derivatized surfaces in a wide variety of immunofluorescence applications such as immunochemistry and histochemistry. Streptavidin-R-Phycoerythrin may be used in the development of bioassay devices such as Lab-on-a-chip (LoC) systems and microarrays.
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Min Sun et al.
Steroids, 75(13-14), 1089-1096 (2010-07-27)
The small blood volumes available in rodent studies often limit adequate quantification of all hormones of interest. We report here the development of two new assays combining an extraction step with multiplex immunoassay (MIA) technology for the simultaneous determination of
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Point-of-care (PoC) testing followed by personalized efficient therapy of infectious diseases may result in a considerable reduction of associated health care costs. Lab-on-a-chip (LoC) systems represent a potentially high efficient class of PoC tools. Here, we present a LoC system
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Clinical chemistry, 52(6), 1033-1039 (2006-03-25)
Genotyping of N-acetyltransferase-2 (NAT2) is useful in predicting the risk for toxicity of NAT2 substrates. Current methods cannot detect the 7 most important single-nucleotide variations in NAT2 simultaneously in 1 tube. We developed an assay that uses allele-specific primer extension
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Malaria journal, 19(1), 188-188 (2020-05-26)
While sub-microscopic malarial infections are frequent and potentially deleterious during pregnancy, routine molecular detection is still not feasible. This study aimed to assess the performance of a Histidine Rich Protein 2 (HRP2)-based ultrasensitive rapid diagnostic test (uRDT, Alere Malaria Ag
Adam Stewart et al.
Methods in molecular biology (Clifton, N.J.), 1636, 119-131 (2017-07-22)
The study of protein phosphorylation is critical for the advancement of our understanding of cellular responses to external and internal stimuli. Phosphorylation, the addition of phosphate groups, most often occurs on serine, threonine, or tyrosine residues due to the action
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