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A4800

Sigma-Aldrich

Agar

Type M, suitable for plant cell culture

Synonym(e):

Agar-Agar

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About This Item

Lineare Formel:
(C12H18O9)n
CAS-Nummer:
9002-18-0
EG-Nummer:
232-658-1
MDL-Nummer:
MFCD00081288
UNSPSC-Code:
50405901
eCl@ss:
42040102
NACRES:
NA.21

Biologische Quelle

algae (Rhodophyceae)

Qualitätsniveau

200

Typ

Type M

Form

powder

Methode(n)

cell culture | plant: suitable

Übergangstemp.

transition temp 34-36 °C

Anwendung(en)

agriculture

Lagertemp.

room temp

InChI

1S/C14H24O9/c1-5-8(16)13-11(7(21-5)4-20-13)23-14-10(18)12(19-2)9(17)6(3-15)22-14/h5-18H,3-4H2,1-2H3/t5?,6-,7?,8-,9+,10-,11?,12+,13+,14?/m1/s1

InChIKey

GYYDPBCUIJTIBM-DYOGSRDZSA-N

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Allgemeine Beschreibung

Type M agar is predominantly used in plant tissue culture. It is similar to agar, a polysaccharide complex with a backbone of alternating agarose and agaropectin molecules and extracted from red algae.

Anwendung

Type M agar has been used as a component of Murashige and Skoog (MS) medium for culturing Arabidopsis thalania seeds. It has also been used in rooting media for tomato (Solanum lycopersicum) seeds.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

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Murashige-Skoog-Basalmedium powder, suitable for plant cell culture

Sigma-Aldrich

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Murashige-Skoog-Basalmedium

Sangeeta Negi et al.
The Plant journal : for cell and molecular biology, 61(1), 3-15 (2009-10-02)
In this study we investigated the role of ethylene in the formation of lateral and adventitious roots in tomato (Solanum lycopersicum) using mutants isolated for altered ethylene signaling and fruit ripening. Mutations that block ethylene responses and delay ripening -Nr
Xiaohua Wang et al.
Nature protocols, 10(12), 2054-2063 (2015-11-20)
Measuring the mobility and interactions of proteins is key to understanding cellular signaling mechanisms; however, quantitative analysis of protein dynamics in living plant cells remains a major challenge. Here we describe an automated, single-molecule protocol based on total internal reflection
Sanjaya B Ekanayake et al.
Methods in molecular biology (Clifton, N.J.), 1305, 223-240 (2015-04-26)
One of the most striking features of plant mitochondria when visualized in living tissue is their dynamism. The beauty of cytoplasmic streaming, driving, and being driven by the motility of mitochondria and other small organelles belies the complexity of the
Arnaud Dechesne et al.
Applied and environmental microbiology, 74(16), 5195-5200 (2008-07-01)
Water is arguably the most important constituent of microbial microhabitats due to its control of physical and physiological processes critical to microbial activity. In natural environments, bacteria often live on unsaturated surfaces, in thin (micrometric) liquid films. Nevertheless, no experimental
Queeny Wing-Han Yuen et al.
The open biomedical engineering journal, 5, 39-46 (2011-06-07)
Cervical lymph nodes are common sites of metastatic involvement in head and neck cancers. These lymph nodes are superficially located and palpation is a common practice for assessing nodal hardness and staging cancer which is, however, too subjective and with
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