A3301
Agargel™
suitable for plant cell culture, powder
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UNSPSC Code:
10171502
eCl@ss:
42040102
NACRES:
NA.72
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General description
Agargel™ is a proprietary blend of agar and phytagel. Phytagel is intended for use in place of agar and other gelling agents for plant tissue culture. Phytagel has been shown to be a superior substitute for tissue-culture-grade agar in the micropropagation of banana plantlets. The typical working concentration is 3.5-5.0 g/L.
Application
Agargel™ has been used:
- as a gelling agent for the solidification of B5 medium to study the effect of the gelling agent at different concentrations on the maturation of avocado somatic embryos
- as a component of the Murashige and Skoog basal medium (BM) to culture terminal and auxiliary buds from V. jatamansi
- for the solidification of the hydroponic solution to grow Arabidopsis thaliana
Other Notes
A proprietary blend of agar and Phytagel™
Legal Information
Agargel is a trademark of Sigma-Aldrich Co. LLC
Phytagel is a trademark of Sigma-Aldrich Co. LLC
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Shoot organogenesis and somatic embryogenesis from leaf explants of Valeriana jatamansi Jones
Chen R, et al.
Scientia Marina, 165, 392-397 (2014)
Water relations in culture media influence maturation of avocado somatic embryos
Belen M, et al.
Journal of Plant Physiology (2011)
Ethylene Response Factor109 Attunes Immunity, Photosynthesis, and Iron Homeostasis in Arabidopsis Leave
Chiu L Y, et al.
Frontiers in Plant Science (2022)
José A Caparrós-Martín et al.
Planta, 237(4), 943-954 (2012-11-28)
This work presents the isolation and the biochemical characterization of the Arabidopsis thaliana gene AtSgpp. This gene shows homology with the Arabidopsis low molecular weight phosphatases AtGpp1 and AtGpp2 and the yeast counterpart GPP1 and GPP2, which have a high
R Medina et al.
Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al, 28(1), 13-20 (2004-06-05)
An efficient clonal propagation procedure for six rice varieties cultivated in Argentina was developed by using shoot tip cultures, and the genetic stability of the micropropagated plants was verified by isozyme analysis. One week old seedlings obtained on MS medium
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