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Merck
CN

MR-121

Sigma-Aldrich

EmbryoMax® KSOM小鼠胚胎培养基

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

别名:

K+ Simplex Optimised Medium (KSOM), KSOM Media

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关于此项目

UNSPSC代码:
12352207
eCl@ss:
32160801
NACRES:
NA.75
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质量水平

表单

liquid

制造商/商品名称

Specialty Media
EmbryoMax®

技术

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

输入

sample type: mouse embryo(s)

应用

EmbryoMax® KSOM小鼠胚胎培养基已用于小鼠胚胎的采集。

制备说明

可以在-20°C下保存直至瓶上的有效期。


解冻后应在2周内使用。

法律信息

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

免责声明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

储存分类代码

12 - Non Combustible Liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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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
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
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

商品

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.

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

用于转基因小鼠胚胎培养的小鼠胚胎培养基及经过胚胎培养验证的试剂

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