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Merck

S6940

Sigma-Aldrich

SigmaScreen Streptavidin High Capacity Coated Plates

96 well clear

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About This Item

Kod UNSPSC:
12352204
NACRES:
NA.83

Materiały

polystyrene

Poziom jakości

opis

flat bottom

temp. przechowywania

2-8°C

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Opis ogólny

SigmaScreen Streptavidin coated high capacity plates utilize a proprietary coating technology which provides substantially greater biotin binding capacity than standard Streptavidin or ExtrAvidin coated plates. This clear, 96-well plate has a format of breakable 8-well strips on a single-well holding frame, and has a binding capacity of ≥ 15 pmol/well. Streptavidin coated high capacity plates provide a platform which allows the captured protein to be eluted for post-capture analysis by various methods such as MALDI, ICAT or SDS-PAGE.

Informacje prawne

SigmaScreen is a trademark of Sigma-Aldrich Co. LLC
This page may contain text that has been machine translated.

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)


Certyfikaty analizy (CoA)

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Hong-Sheng Lim et al.
Journal of immunology (Baltimore, Md. : 1950), 195(11), 5432-5439 (2015-10-27)
Optimal T cell activation typically requires engagement of both the TCR and costimulatory receptors, such as CD28. Engagement of CD28 leads to tyrosine phosphorylation of its cytoplasmic region and recruitment of cytoplasmic signaling proteins. Although the exact mechanism of CD28
Lu Li et al.
Analytica chimica acta, 886, 123-132 (2015-09-01)
A method for fabrication of multiplexed optical coding nanobeads (MOCNBs) was developed by hybridizing three types of coding DNAs labeled with different dyes (Cy5, FAM and AMCA) at precisely controlled ratios with biotinylated reporter DNA modified to magnetic streptavidin-coated nanobeads
Román González-Prieto et al.
Cell reports, 34(4), 108691-108691 (2021-01-28)
In contrast to our extensive knowledge on covalent small ubiquitin-like modifier (SUMO) target proteins, we are limited in our understanding of non-covalent SUMO-binding proteins. We identify interactors of different SUMO isoforms-monomeric SUMO1, monomeric SUMO2, or linear trimeric SUMO2 chains-using a
Yasmin ElTahir et al.
BMC molecular and cell biology, 20(1), 55-55 (2019-12-01)
Brucella is a facultative intracellular pathogen responsible for zoonotic disease brucellosis. Little is known about the molecular basis of Brucella adherence to host cells. In the present study, the possible role of Bp26 protein as an adhesin was explored. The
Jie Wang et al.
Nature, 569(7757), 509-513 (2019-05-10)
A universal gain-of-function approach for selective and temporal control of protein activity in living systems is crucial to understanding dynamic cellular processes. Here we report development of a computationally aided and genetically encoded proximal decaging (hereafter, CAGE-prox) strategy that enables time-resolved

Produkty

Modyfikacje białek są kluczowe dla badania chorób. Metody analizy są kluczowe.

Protein modifications are crucial for disease study. Analysis methods are key.

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