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Agitateur magnétique

for use with For 3.0-5.0mL vessels, pkg of 6 ea, PTFE

Synonyme(s) :

AGITATEURS MAGNETIQUES 3,5 ML À 6 ML M.V. BOÎTE DE 6

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About This Item

Code UNSPSC :
41103806

Matériaux

PTFE
triangular PTFE-coated

Conditionnement

pkg of 6 ea

Compatibilité

for use with For 3.0-5.0mL vessels

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Informations légales

WHEATON is a registered trademark of Wheaton Industries, Inc.

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Shuo Liu et al.
Cell, 176(3), 491-504 (2019-01-08)
Increased protein synthesis plays an etiologic role in diverse cancers. Here, we demonstrate that METTL13 (methyltransferase-like 13) dimethylation of eEF1A (eukaryotic elongation factor 1A) lysine 55 (eEF1AK55me2) is utilized by Ras-driven cancers to increase translational output and promote tumorigenesis in vivo.
Ying Li et al.
Neural regeneration research, 16(7), 1308-1316 (2020-12-16)
Previous studies demonstrate an accumulation of transferrin and transferrin receptor 1 (TfR1) in regenerating peripheral nerves. However, the expression and function of transferrin and TfR1 in the denervated skeletal muscle remain poorly understood. In this study, a mouse model of
Ricardo Usategui-Martín et al.
Molecular therapy. Methods & clinical development, 17, 1155-1166 (2020-06-10)
Retinal photoreceptor degeneration occurs frequently in several neurodegenerative retinal diseases such as age-related macular degeneration, retinitis pigmentosa, or genetic retinal diseases related to the photoreceptors. Despite the impact on daily life and the social and economic consequences, there is no
Prerana Ramadurgum et al.
Cell chemical biology, 27(5), 622-634 (2020-04-25)
Destabilizing domains (DDs), such as a mutated form of Escherichia coli dihydrofolate reductase (ecDHFR), confer instability and promote protein degradation. However, when combined with small-molecule stabilizers (e.g., the antibiotic trimethoprim), DDs allow positive regulation of fusion protein abundance. Using a combinatorial screening
Jonathan Martinez-Fabregas et al.
Cell reports, 33(12), 108545-108545 (2020-12-29)
Cytokines are highly pleiotropic ligands that regulate the immune response. Here, using interleukin-6 (IL-6) as a model system, we perform detailed phosphoproteomic and transcriptomic studies in human CD4+ T helper 1 (Th-1) cells to address the molecular bases defining cytokine

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