69449
BL21 Competent Cells - Novagen
BL21 host strain is the most widely used host background and has the advantage of being deficient in both lon and ompT proteases.
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About This Item
Produtos recomendados
fonte biológica
Escherichia coli
Nível de qualidade
fabricante/nome comercial
Novagen®
condição de armazenamento
OK to freeze
avoid repeated freeze/thaw cycles
modo de crescimento
adherent or suspension
morfologia
rod shaped
técnica(s)
microbiological culture: suitable
transformação celular
transformation efficiency: >2×107 cfu/μg
Condições de expedição
dry ice
temperatura de armazenamento
−70°C
Categorias relacionadas
Descrição geral
BL21 host strain is the most widely used host background and has the advantage of being deficient in both lon and ompT proteases.
BL21 is the most widely used host background and has the advantage of being deficient in both lon (1) and ompT proteases.
This product contains genetically modified organisms (GMO). Within the EU GMOs are regulated by Directives 2001/18/EC and 2009/41/EC of the European Parliament and of the Council and their national implementation in the member States respectively. This legislation obliges us to request certain information about you and the establishment where the GMOs are being handled. Click here for Enduser Declaration (EUD) Form.
Componentes
0.4 ml1 mlComponent
•2 × 0.2 ml5 × 0.2 mlBL21 Competent Cells
•2 × 2 ml4 × 2 mlSOC Medium
•10 µl10 µlTest Plasmid
•2 × 0.2 ml5 × 0.2 mlBL21 Competent Cells
•2 × 2 ml4 × 2 mlSOC Medium
•10 µl10 µlTest Plasmid
Advertência
Toxicity: Multiple Toxicity Values, refer to MSDS (O)
Outras notas
1. Phillips, T. A., Van Bogelen, R. A., and Neidhardt, F. C. (1984) J. Bacteriol.
159, 283–287.
159, 283–287.
Informações legais
NOVAGEN is a registered trademark of Merck KGaA, Darmstadt, Germany
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 2
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Developmental cell, 41(2), 143-156 (2017-04-26)
The spindle assembly checkpoint kinase Mps1 not only inhibits anaphase but also corrects erroneous attachments that could lead to missegregation and aneuploidy. However, Mps1's error correction-relevant substrates are unknown. Using a chemically tuned kinetochore-targeting assay, we show that Mps1 destabilizes microtubule attachments
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