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Merck

K4003

Sigma-Aldrich

Knudson C 改良兰花培养基

powder, suitable for plant cell culture

别名:

改良 KC 兰花培养基

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About This Item

分類程式碼代碼:
12352207
NACRES:
NA.72

應用

Knudson C 改良兰花培养基是兰科植物种子萌发的营养液。这种培养基通常添加 100-150g 香蕉,或 100-200 mL 椰子汁,每升 2g 蔬菜炭。

公式變體

使用 Knudson (1946) 描述的宏量和微量营养素。含蔗糖。

培养基配方

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Philip J Kauth et al.
Annals of botany, 102(5), 783-793 (2008-09-02)
Ecotypic differentiation has been explored in numerous plant species, but has been largely ignored in the Orchidaceae. Applying a specific germination protocol for widespread seed sources may be unreliable due to inherent physiological or genetic differences in localized populations. It
Guek Eng Sim et al.
Plant cell reports, 26(4), 383-393 (2006-10-07)
We have successfully developed a method to induce early in vitro flowering of the self-pollinated seedlings of a tropical orchid hybrid, Dendrobium Madame Thong-In. Transition of vegetative shoot apical meristem to inflorescence meristem was observed when young protocorms were cultured
E Ouni et al.
Human reproduction (Oxford, England), 35(6), 1391-1410 (2020-06-17)
How do elastic matrisome components change during the lifetime of the human ovary? The deposition and remodeling of mechanical matrisome components (collagen, elastin, elastin microfibril interface-located protein 1 (EMILIN-1), fibrillin-1 and glycosaminoglycans (GAGs)) that play key roles in signaling pathways
Kate Lykke Lambertsen et al.
PloS one, 7(10), e47744-e47744 (2012-10-19)
The calmodulin/calcium-activated K(+) channel KCa3.1 is expressed in red and white blood cells, epithelia and endothelia, and possibly central and peripheral neurons. However, our knowledge about its contribution to neurological functions and behavior is incomplete. Here, we investigated whether genetic
Satotaka Omori et al.
Cell metabolism, 32(5), 814-828 (2020-09-20)
Cell senescence plays a key role in age-associated organ dysfunction, but the in vivo pathogenesis is largely unclear. Here, we generated a p16-CreERT2-tdTomato mouse model to analyze the in vivo characteristics of p16high cells at a single-cell level. We found tdTomato-positive p16high

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