Cell Dissociation Solution Non-enzymatic 1x

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

MDL number:

Quality Level



product line





1 ×


cell culture | mammalian: suitable



shipped in

wet ice

storage temp.

room temp

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General description

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


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


100 mL in poly bottle


NONH for all modes of transport

WGK Germany


Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

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)
Comparison of enzymatic and non-enzymatic means of dissociating adherent monolayers of mesenchymal stem cells
Heng BC, et al.
Biological Procedures Online, 11(1), 161-161 (2009)
Antitumor efficacy of a bispecific antibody that targets HER2 and activates T cells.
Junttila TT, Li J, Johnston J, et al.
Cancer Research, 74(19), 5561-5571 (2014)
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)....
Combinatorial treatment of mammospheres with trastuzumab and salinomycin efficiently targets HER2-positive cancer cells and cancer stem cells
Oak PS, et al.
International Journal of Cancer. Journal International Du Cancer, 131(12), 2808-2819 (2012)

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