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M9274

Sigma-Aldrich

Milieu de base de Murashige et Skoog

suitable for plant cell culture, with sucrose and agar

Synonyme(s) :

Milieu de base MS

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About This Item

Numéro MDL:
MFCD00240976
Code UNSPSC :
12352207
Nomenclature NACRES :
NA.72

Niveau de qualité

200

Forme

powder

Technique(s)

cell culture | plant: suitable

Application(s)

agriculture

Conditions d'expédition

ambient

Température de stockage

2-8°C

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Application

Murashige and Skoog Basal Medium has been used for culturing Arabidopsis transgenic seeds for cotyledon development, pearl millet (Pennisetum glaucum), and Rosmarinus ofcinalis L. for callus induction

Variante de formule

With the macro- and micronutrients, vitamins, sucrose and agar as described by Murashige and Skoog (1962).

Media Formulation

Quantité

Formulated to contain 42.4 grams of powder per liter of medium.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

08168

Timestrip Plus™ 8 °C

Pictogrammes

Flame over circleExclamation mark
GHS03,GHS07

Mention d'avertissement

Warning

Mentions de danger

H272,H319

Classification des risques

Eye Irrit. 2 - Ox. Sol. 3

Code de la classe de stockage

5.1B - Oxidizing hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Antoine Fort et al.
The New phytologist, 209(2), 590-599 (2015-09-24)
Heterosis is the phenomenon whereby hybrid offspring of genetically divergent parents display superior characteristics compared with their parents. Although hybridity and polyploidy can influence heterosis in hybrid plants, the differential contributions of hybridity vs polyploidy to heterosis effects remain unknown.
Laure Audonnet et al.
Gene expression patterns : GEP, 25-26, 1-7 (2017-04-13)
Dimethylation of histone H3 lysine 9 (H3K9me2) is a heterochromatic mark linked to DNA methylation and gene repression. Removal of H3K9me2 from gene bodies by the jmjC histone demethylase IBM1/JMJ25 inhibits DNA methylation and derepresses gene expression. In this work
Iram Siddique et al.
Applied biochemistry and biotechnology, 162(7), 2067-2074 (2010-05-13)
An effective protocol was developed for in vitro regeneration of the Cassia angustifolia via indirect organogenesis from petiole explants excised from 21-day-old axenic seedlings. Organogenic callus were induced on Murashige and Skoog (MS) medium supplemented with 5.0 µM 2,4-dichlorophenoxy acetic acid
Smita P Chavan et al.
Applied microbiology and biotechnology, 89(6), 1701-1707 (2010-12-02)
The present study examined the effects of plant growth hormones, incubation period, biotic (Trametes versicolor, Mucor sp., Penicillium notatum, Rhizopus stolonifer, and Fusarium oxysporum) and abiotic (NaCl, MgSO(4), FeSO(4), ZnSO(4), and FeCl(3)) elicitors on cell growth and α-tocopherol and pigment
K Sopalun et al.
Cryo letters, 31(4), 347-357 (2010-09-08)
Three vitrification-based methods for the cryopreservation of Grammatophyllum speciosum protocorms were invesigated: droplet-vitrification, encapsulation-dehydration and encapsulation-vitrification. Protocorms, 0.1 cm in diameter, developed from 2-month-old germinating seeds were used. For droplet-vitrification, protocorms were precultured on filter paper soaked in half strength
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