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无菌性
sterile-filtered
表单
liquid
浓度
100 ×
技术
cell culture | plant: suitable
颜色
yellow
pH值（酸碱度）
4.0-6.5
应用
agriculture
运输
dry ice
储存温度
−20°C
相关类别
一般描述
Kao and Michayluk Vitamin Solution K3129是Kao & Michayluk培养基的100倍浓缩液。可与Kao& Michayluk盐一起用于配制Kao&Michayluk培养基。
应用
Kao and Michayluk Vitamin Solution 已被用于：
- 作为培养基补充剂
- 诱导液体海盐介质中的愈伤组织，测试 MOLA115培养物的需求量
- 作为LeMaster培养基的成分
重悬
以每升预制培养基 10mL 的浓度使用，以达到合适的最终浓度。
储存分类代码
12 - Non Combustible Liquids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
其他客户在看
Clémence Bonnot et al.
The New phytologist, 223(2), 993-1008 (2019-04-05)
ROOT HAIR DEFECTIVE SIX-LIKE (RSL) genes control the development of structures from single cells at the surface of embryophytes (land plants) such as rhizoids and root hairs. RSL proteins constitute a subclass (VIIIc) of the basic helix-loop-helix (bHLH) class VIII
Irnov Irnov et al.
PLoS genetics, 13(8), e1006978-e1006978 (2017-08-23)
To achieve robust replication, bacteria must integrate cellular metabolism and cell wall growth. While these two processes have been well characterized, the nature and extent of cross-regulation between them is not well understood. Here, using classical genetics, CRISPRi, metabolomics, transcriptomics
Pleionea mediterranea gen. nov., sp. nov., a gammaproteobacterium isolated from coastal seawater
Fagervold SK, et al.
International Journal of Systematic and Evolutionary Microbiology, 63(7), 2700-2705 (2013)
Michael R Davey et al.
Methods in molecular biology (Clifton, N.J.), 318, 201-210 (2006-05-06)
The family Passifloraceae contains many species exploited in the food, pharmaceutical, and ornamental plant industries. The routine culture of isolated protoplasts (naked cells) followed by reproducible plant regeneration, is crucial to the genetic improvement of Passiflora spp. by somatic cell
Likyelesh Gugsa et al.
Biotechnology research international, 2011, 309731-309731 (2011-10-27)
Tef (Eragrostis tef) provides a major source of human nutrition in the Horn of Africa, but biotechnology has had little impact on its improvement to date. Here, we report the elaboration of an in vitro regeneration protocol, based on the
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