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C5789

Sigma-Aldrich

Cell Dissociation Solution Non-enzymatic 1x

Prepared in Hanks′ Balanced Salt Solution without calcium and magnesium, sterile-filtered, BioReagent, suitable for cell culture

Sinonimo/i:

Cell Dissociation Reagent

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100 ML
CHF 103.00

CHF 103.00


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100 ML
CHF 103.00

About This Item

Numero MDL:
Codice UNSPSC:
12352204
NACRES:
NA.75

CHF 103.00


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Livello qualitativo

Sterilità

sterile-filtered

Nome Commerciale

BioReagent

Stato

solution

Concentrazione

1 ×

tecniche

cell culture | mammalian: suitable

pH

6.5-7.5

Condizioni di spedizione

wet ice

Temperatura di conservazione

room temp

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Descrizione generale

Cell Dissociation Solution Non-enzymatic buffer systems are alternative to the canonical trypsin based buffers for dissociation of adherent mesenchymal stem cell (MSC) monolayers.[1]

Applicazioni

Cell Dissociation Solution Non-enzymatic 1x has been used in the dissociation of murine macrophage (RAW2647) cells,[2] A549 pulmonary cells,[3] islets cells[4] and 2D cell and 3D mammospheres.[5]
Special non-enzymatic formulation for gently dislodging adherent cell types from plastic or glass surfaces.

Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1


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Differential effects of RU486 reveal distinct mechanisms for glucocorticoid repression of prostaglandin E2 release
Chivers JE, et al.
European Journal of Biochemistry, 271(20), 4042-4052 (2004)
Jiaoying Jia et al.
Frontiers in cell and developmental biology, 9, 621187-621187 (2021-08-07)
Dysfunctions of neural stem cells (NSCs) often lead to a variety of neurological diseases. Thus, therapies based on NSCs have gained increasing attention recently. It has been documented that microRNA (miR)-421 represses the autophagy and apoptosis of mouse hippocampal neurons
Rosa G M Lammerts et al.
Frontiers in immunology, 11, 1643-1643 (2020-08-28)
Introduction: Proteinuria contributes to progression of renal damage, partly by complement activation on proximal tubular epithelial cells. By pattern recognition, properdin has shown to bind to heparan sulfate proteoglycans on tubular epithelium and can initiate the alternative complement pathway (AP).
Impact of integrin-matrix matching and inhibition of apoptosis on the survival of purified human beta-cells in vitro
Ris F, et al.
Diabetologia, 45(6), 841-850 (2002)
Evidence for lipopolysaccharide induced differentiation of RAW264. 7 murine macrophage cell line into dendritic like cells
Saxena RK, et al.
Journal of Biosciences, 28(1), 129-134 (2003)

Questions

1–2 of 2 Questions  
  1. Hi, I am working with primary microglia and it very tricky to dissociate. I usually dissociate them with 0.5% Trypsin for 7 min at 37˚C and still hard to collect them. May I know whether this reagent would be a better alternative? Thank you!

    1 answer
    1. This product contains EDTA as the major active component, which acts as a chelating agent for divalent cations to loosen cell–cell contacts but does not break down the extracellular matrix as trypsin does. Empirical testing is needed to determine if this approach is more effective. It is highly recommended to review the literature to determine if an EDTA-only dissociation method has been successfully used with the particular primary microglia preparation protocol.

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  2. What is the concentration of EDTA in Cat#C5789? Thanks

    1 answer
    1. The concentration of EDTA in this formulation is proprietary. Additional components include Sodium Citrate, Nitrilotriacetic Acid, and Glycerol in Hank's Balanced Salt solution. Should the concentration of EDTA be required, product E8008, EDTA 0.2% in DPBS, may be of interest. Both items are tested for cell dissociation. Please see the link below to review this product option:
      https://www.sigmaaldrich.com/US/en/product/sigma/e8008

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