S2438
Streptavidin−Peroxidase Polymer, Ultrasensitive
Synonyme(s) :
Highly sensitive Streptavidin−Peroxidase
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NACRES:
NA.32
UNSPSC Code:
12352202
Service technique
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Laissez-nous vous aiderGeneral description
Activated streptavidin (SA) and horseradish peroxidase (HRP) are covalently conjugated to a polymer backbone. Multiple active biomolecules on each polymer chain increase the biotin binding capacity and amplify the peroxidase enzyme signal.
Application
Detection of biotinylated proteins and nucleic acids and other biomolecules.
Suitable use in Western blotting and ELISA and for detecting surface antigens in immunohistochemistry and immunocytochemistry.
Suitable use in Western blotting and ELISA and for detecting surface antigens in immunohistochemistry and immunocytochemistry.
Biochem/physiol Actions
Biotinylated biomolecules.
Physical form
Supplied as an 1.0 mg/ml solution in 0.01 M sodium phosphate, 0.15 M sodium chloride, 50% glycerol, stabilizer and preservative, pH 7.4.
Classe de stockage
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Contenu apparenté
Datasheet
Natalia Gruba et al.
International journal of molecular sciences, 20(7) (2019-03-31)
Kallikrein 13 (KLK13) was first identified as an enzyme that is downregulated in a subset of breast tumors. This serine protease has since been implicated in a number of pathological processes including ovarian, lung and gastric cancers. Here we report
Stefan Kaluz et al.
Biochemical and biophysical research communications, 370(4), 613-618 (2008-04-12)
The hypoxia-inducible factor (HIF) activates transcription via binding to the highly variable hypoxia-responsive elements (HREs). All hypoxia-inducible constructs described to date utilize multimers of naturally occurring HREs. Here, we describe the rational design of minimal hypoxia-inducible enhancers, conceptually equivalent to
Jaclyn C Law et al.
Journal of immunology (Baltimore, Md. : 1950), 206(1), 37-50 (2020-11-20)
There is a pressing need for an in-depth understanding of immunity to SARS-CoV-2. In this study, we investigated human T cell recall responses to fully glycosylated spike trimer, recombinant N protein, as well as to S, N, M, and E