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S6940

Sigma-Aldrich

SigmaScreen™ Streptavidin High Capacity Coated Plates

96 well clear

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About This Item

UNSPSC Code:
12352204
NACRES:
NA.83

material

polystyrene

Quality Level

200

description

flat bottom

storage temp.

2-8°C

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General description

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.

Legal Information

SigmaScreen is a trademark of Sigma-Aldrich Co. LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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

Articles

Post Translational Modification

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

Post Translational Modification

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

Post Translational Modification

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

Post Translational Modification

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

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