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Merck

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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About This Item

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

form

liquid

manufacturer/tradename

Specialty Media, EmbryoMax®

technique(s)

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

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)

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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"As transgenic mouse core laboratories know well, mouse models are a powerful means of determining the function of mammalian genes in the context of whole organisms—especially since over 95% of the mouse genome is similar to the human genome. However, you may not know that: 1. Laboratory mouse strains are descended from ancestors in modern-day Pakistan. 2. The first inbred strain of lab mouse was created in 1909. It was named DBA for its coat color: dilute brown non-agouti. 3. There is a mutant mouse actually named“Bad Hair Day” (Bhrd). Someone get this little guy a stylist! 4. Male mice, when treated with anticancer drugs, have been shown to pass on DNA instability to their offspring. 5. The founder of Jackson Laboratories, C. C. Little, once had lunch with Walt Disney to request that an animated film be created linking Mickey Mouse and the laboratory mouse. The request was denied."


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



Global Trade Item Number

SKUGTIN
MR-004-D04053252504600