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MilliporeSigma

MR-004

EmbryoMax® Acidic Tyrode′s Solution

The EmbryoMax Acidic Tyrode′s Solution is available in a 50 mL format and has been optimized and validated for Embryo Culture.

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50 ML

$54.50

$54.50


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About This Item

UNSPSC Code:
12352207
NACRES:
NA.75
eCl@ss:
32160801
Form:
liquid

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form

liquid

manufacturer/tradename

Specialty Media, EmbryoMax®

technique(s)

cell culture | embryo: suitable, cell culture | stem cell: suitable

input

sample type: mouse embryo(s)

Quality Level

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TMS-002ES-003MR-024
Quality Level

300

Quality Level

200

Quality Level

200

Quality Level

300

form

liquid

form

liquid

form

liquid

form

liquid

manufacturer/tradename

Specialty Media

manufacturer/tradename

Specialty Media, EmbryoMax®

manufacturer/tradename

Specialty Media, EmbryoMax®

manufacturer/tradename

Specialty Media, EmbryoMax®

technique(s)

cell culture | embryo: suitable

technique(s)

cell culture | stem cell: suitable

technique(s)

cell culture | stem cell: suitable

technique(s)

cell culture | embryo: suitable, cell culture | stem cell: suitable

input

sample type: mouse embryo(s)

input

sample type: mouse embryonic stem cell(s)
sample type induced pluripotent stem cell(s)

input

sample type: mouse embryonic stem cell(s)
sample type induced pluripotent stem cell(s)

input

sample type: mouse embryo(s)

General description

This solution is designed for the removal of Zonae pellucidae from mouse oocytes.

Preparation Note

Store at -20°C upto 2 months & 1 day

Legal Information

EmbryoMax is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Hiroyuki Hirai et al.
Stem cells (Dayton, Ohio), 29(9), 1349-1361 (2011-07-07)
Induced pluripotent stem cells (iPSCs) can be created by reprogramming differentiated cells through introduction of defined genes, most commonly Oct4, Sox2, Klf4, and c-Myc (OSKM). However, this process is slow and extremely inefficient. Here, we demonstrate radical acceleration of iPSC

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