S6940
SigmaScreen™ Streptavidin High Capacity Coated Plates
96 well clear
Faça loginpara ver os preços organizacionais e de contrato
Selecione um tamanho
1 EA
R$ 695,00
5 X 1 EA
R$ 5.951,00
R$ 695,00
Check Cart for Availability
Selecione um tamanho
Alterar visualização
1 EA
R$ 695,00
5 X 1 EA
R$ 5.951,00
About This Item
Código UNSPSC:
12352204
NACRES:
NA.83
R$ 695,00
Check Cart for Availability
Produtos recomendados
![[Glu1]-Fibrinopeptide B human ≥90% (HPLC)](/deepweb/assets/sigmaaldrich/product/structures/122/537/7ead5c32-cb67-4325-9ce7-66c8dec24bdd/640/7ead5c32-cb67-4325-9ce7-66c8dec24bdd.png)
Materiais
polystyrene
Nível de qualidade
descrição
flat bottom
tamanho
96 wells
temperatura de armazenamento
2-8°C
Procurando produtos similares? Visita Guia de comparação de produtos
Categorias relacionadas
Descrição geral
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.
Informações legais
SigmaScreen is a trademark of Sigma-Aldrich Co. LLC
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
Escolha uma das versões mais recentes:
Já possui este produto?
Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
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
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
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
Artigos
Protein modifications are crucial for disease study. Analysis methods are key.
Active Filters
Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.
Entre em contato com a assistência técnica
