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MR-121

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EmbryoMax® KSOM Mouse Embryo Media

(1X), Liquid, with 1/2 Amino Acids & Phenol Red

Synonym(s):

K+ Simplex Optimised Medium (KSOM), KSOM Media

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About This Item

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

Quality Level

300

form

liquid

manufacturer/tradename

Specialty Media
EmbryoMax®

technique(s)

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

input

sample type: mouse embryo(s)

Application

EmbryoMax® KSOM Mouse Embryo Media has been used in the collection of mice embryos.

Storage and Stability

Can be stored at -20°C upto the expiration date on the bottle.
Once thawed it should be used within 2 weeks.

Note: Our EmbryoMax Liquid Mouse Embryo Media is produced on a bi-monthly basis. For regular users, we encourage standing orders to ensure that backorders do not occur.

Legal Information

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

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Chao-Lien Liu et al.
The Journal of biological chemistry, 282(2), 1109-1118 (2006-11-17)
l(2)dtl (lethal (2) denticleless), is an embryonic lethal homozygous mutation initially identified in Drosophila melanogaster that produces embryos that lack ventral denticle belts. In addition to nucleotide sequence, bioinformatic analysis has revealed a conservation of critical functional motifs among the
Christiana Kyvelidou et al.
Journal of structural biology, 176(3), 379-386 (2011-10-04)
Embryo patterning is subject to intense investigation. So far only large, microscopically obvious structures like polar body, cleavage furrow, pro-nucleus shape can be evaluated in the intact embryo. Using non-linear microscopic techniques, the present work describes new methodologies to evaluate
A potential use of embryonic stem cell medium for the in vitro culture of preimplantation embryos.
Gelber K. et al.
Journal of Assisted Reproduction and Genetics null
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
Dae-In Ha et al.
Experimental & molecular medicine, 52(11), 1823-1830 (2020-11-10)
The CRISPR-Cas12a system has been developed to harness highly specific genome editing in eukaryotic cells. Given the relatively small sizes of Cas12a genes, the system has been suggested to be most applicable to gene therapy using AAV vector delivery. Previously
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Articles

Development of a New Advanced KSOM Mouse Embryo Media that Enables Dual-Use Embryo Culture and Cell Handling Applications

Advanced KSOM mouse embryo media that can be used as a single medium for both harvest and culture of mouse embryos to facilitate creation of transgenic knockout mice.

Embryo Culture Media

Mouse embryo media and embryo validated reagents for transgenic mouse embryo culture

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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