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Documenti fondamentali

M0518

Sigma-Aldrich

Terreno essenziale minimo di Eagle

Joklik Modification, with L-glutamine, without calcium chloride and sodium bicarbonate, suitable for cell culture

Sinonimo/i:

Joklik Modified MEM, MEM

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About This Item

Codice UNSPSC:
12352207
NACRES:
NA.75

Livello qualitativo

Stato

powder

tecniche

cell culture | mammalian: suitable

Componenti

HEPES: no
sodium pyruvate: no
L-glutamine: yes
NaHCO3: no
phenol red: yes

Condizioni di spedizione

ambient

Temperatura di conservazione

2-8°C

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Applicazioni

Recommended for suspension cultures.

Quantità

Formulated to contain 11.0 grams of powder per liter of medium.

Ricostituzione

Supplement with 2.0 g/L sodium bicarbonate.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

Lot/Batch Number

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Chronic kidney disease (CKD) is accompanied by cardiac fibrosis, hypertrophy, and dysfunction, which are commonly referred to as uremic cardiomyopathy. Our previous studies found that Na/K-ATPase ligands or 5/6th partial nephrectomy (PNx) induces cardiac fibrosis in rats and mice. The
Francesca Rivello et al.
Science advances, 6(40) (2020-10-02)
Despite their important role in metastatic disease, no general method to detect circulating stromal cells (CStCs) exists. Here, we present the Metabolic Assay-Chip (MA-Chip) as a label-free, droplet-based microfluidic approach allowing single-cell extracellular pH measurement for the detection and isolation
Winston T Stauffer et al.
International journal of molecular sciences, 21(4) (2020-02-23)
Activating transcription factor-6 α (ATF6) is one of the three main sensors and effectors of the endoplasmic reticulum (ER) stress response and, as such, it is critical for protecting the heart and other tissues from a variety of environmental insults
Kevin T James et al.
Scientific reports, 6, 36826-36826 (2016-11-09)
Viruses are extensively studied as pathogens and exploited as molecular tools and therapeutic agents. Existing methods to purify viruses such as gradient ultracentrifugation or chromatography have limitations, for example demand for technical expertise or specialized equipment, high time consumption, and

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