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ES-101

COMPLETE ES CELL MEDIUM W/ 15% FBS AND LIF

Ready to use medium formulated with 15% fetal bovine serum (FBS) and mouse leukemia inhibitory factor (LIF). Each lot is qualified for mouse embryonic stem (ES) cell culture.

Synonyme(s) :

ES Cell Culture Medium

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A propos de cet article

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

400

form

liquid

manufacturer/tradename

Specialty Media

technique(s)

cell culture | mammalian: suitable

input

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

General description

Complete ES Cell medium W/ 15% FBS and LIF is suitable for use with mouse embryonic stem (ES) cells. It also works as a complete medium for the growth of primary mouse embryonic fibroblast (PMEF) feeder cells.

Application

Complete ES Cell medium W/ 15% FBS and LIF has been used to culture mouse cranial neural crest cell line (CNCCs). It has also been used to culture mouse embryonic stem cells.

Physical form

Ready to use medium for culture of mouse pluripotent stem (ES and iPS) cells and feeders

Preparation Note

Store at -20°C. After thaw, the medium may be stored at 2-8°C for up to 1 month. Protect from light.

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.

Classe de stockage

10 - Combustible liquids

wgk

WGK 1

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Contenu apparenté

STEMCCA Lentivirus Reprogramming Kits

Millipore’s new STEMCCA lentivirus reprogramming kits make it easier than ever to generate induced pluripotent stem (iPS) cells. Unlike traditional iPS generation which requires simultaneous co-infection by four separate expression vectors, the STEMCCA kits use a single polycistronic lentiviral vector to improve efficiency and reduce the number of viral integrations. The STEMCCA vector is comprised of the transcription factors Oct-4, Klf4, SOX-2, and c-Myc (OKSM), separated by the self-cleaving 2A peptide and IRES sequences 1,2. It is also available with flanking LoxP sites incorporated for Cre-mediated excision of the exogenous reprogramming transgenes. STEMCCA Vector Advantages: (1) Efficient: uses a single vector with four transcription factors rather than co-transducing four separate expression vectors (2) Minimizes viral integrations: single vector reduces the risks of insertional mutagenesis and viral reactivation and (3) Excisable: Cre/LoxP-regulated version enables removal of reprogramming transgenes.

Murine Embryonic Stem Cell Culture Procedures & Protocols

The cell culture protocols described in this instructional manual include the in vitro culture of murine ES cells using EmbryoMax products along with ESGRO® mLIF medium supplement, as well as feeder-free and serum-free ES cell culture using the ESGRO Complete™ line of products. Also included in this instructional manual are: methods for serum-free neuronal differentiation of mouse ES cells, iPS cell generation using STEMCCA™ lentivirus kits, cre-recombinase mediated excision of STEMCCA™ genes from iPS cells, derivation and rescue of new and existing ES cell lines using RESGRO™ Culture Medium and ESGRO Complete™ system.

Issei Saitoh et al.
Cell medicine, 3(1-3), 97-102 (2012-05-08)
Feeder cells are generally required for establishment and maintenance of embryonic stem (ES)/induced pluripotent stem (iPS) cells. Increased demands for generation of those cells carrying various types of vectors (i.e., KO vectors and transgenes) also require feeder cells that confer
Abijeet Singh Mehta et al.
Developmental biology, 471, 97-105 (2020-12-20)
During neurulation, cranial neural crest cells (CNCCs) migrate long distances from the neural tube to their terminal site of differentiation. The pathway traveled by the CNCCs defines the blueprint for craniofacial construction, abnormalities of which contribute to three-quarters of human
Akira Kinoshita et al.
Development (Cambridge, England), 148(16) (2021-08-03)
Mutations in ITPR1 cause ataxia and aniridia in individuals with Gillespie syndrome (GLSP). However, the pathogenic mechanisms underlying aniridia remain unclear. We identified a de novo GLSP mutation hotspot in the 3'-region of ITPR1 in five individuals with GLSP. Furthermore

Numéro d'article de commerce international

RéférenceGTIN
ES-101-B04053252329623