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The effect of basal medium was modified MS> QL>WPM. 基本培养基的效果依次为改良MS> QL >WPM。
The optional inducing medium of adventitious buds is MS basal medium with 2mg/L 6-BA,30g/L sucrose and 9g/L agar. 最佳不定芽诱导培养基为：MS+2mg/L 6-BA+30g/L 蔗糖+9g/L琼脂。
KGF, however, required the presence of a basal medium containing CT, insulin, and serum for optimal proliferation. 然而，要求了包含CT的基本的媒介的出席，胰岛素，并且为最好的增殖的浆液。
Additionally, basal medium + KGF also allowed progression to a distal alveolar phenotype. 额外，基本的媒介+KGF也允许了前进到末梢的齿槽的表现型。
Umbilical cord blood stem cells in the group A were incubated in the endothelial basal medium. A组用内皮细胞基础培养液培养；
The proliferation ratewere 5.02 and 4.25.MS basal medium added 0.5mg/L GA3, 0.lmgIL IAA and O. lmg/L IBA made the shootselongation and better growth. 用MS+0.;1mg/L BA+0
In order to differentiate shoots the N_6 basal medium was added to zeatin(2mg/l), adenine(20mg/l)and lactalbumin hydrolysate(10mg/l). 分化培养基为 N_6附加玉米素(Ze)2.;0mg/l;腺嘌呤20
One-half MS basal medium added 0.1-0.2mg/lNAA or IAA can make the root long and strong. The activated charcoal is good to root formation and growth. 生根培养时，以1/2MS为基本培养基，附加0.;1-0
On the basal medium supplemented with 6-BA 1mg/1 and lactalbumin hydro-lysat 0.2%, the rate of growth and dry weight of mycelium were enhanced. 在基本培养基上添加0.;2%25水解乳蛋白和1毫克/升6-BA的结果;提高了菌丝体的生长速度和干重。
The optional subculture medium is MS basal medium with 2mg/L 2,4-D,40g/L sucrose and lOg/L agar. High sucrose and agar is apt to keep the tight close structure of callus. 最佳继代培养基为：MS+2mg/L 2,4-D+40g/L蔗糖+10g/L琼脂，提高蔗糖及琼脂浓度有利于愈伤组织保持结构紧密的状态。
The stem explants of Fortunella margarita were cultured on MS basal medium supplemented with 1.0 mg/1 BA and 0.1mg/1 IBA for induction of callus and bud formation. 用金桔茎段为外植体;培养在附加1.;0毫克/升BA和0
Adoption of MS basal medium and supplementation of 0.5g/L casamino acids and 0.5g/L glutamine in medium were found to help to facilitate callus induction. 采用MS基本培养基和在培养基中添加0.;5g/L的水解酪蛋白与谷氨酰胺也有助于提高出愈率；
Umbilical cord blood stem cells in the group C were incubated in the endothelial basal medium containing endothelial medium in a 6-well plate coated with fibronectin. C组用添加有内皮细胞培养基的内皮细胞基础培养液在纤维连接蛋白包被的6孔板上培养。
On 1/4 DKW basal medium supplemented no plant growth regulators, the rooting ratio of the top section was 100%, while the middle and basal had no rhizogenesis. 以核桃成熟或近成熟种实子叶为试材，在1/4DKW基本培养基上培养，近胚端的生根率达100%25，而中部和远胚端的生根率为0。
CONCLUSION: MSCs with well growth and rapid proliferation can be detected in the endothelial basal medium containing endothelial medium in an intact 6-well plate. 结论：在未经处理的6孔板上，用添加有内皮细胞培养基的内皮细胞基础培养液细胞培养液可以培养出生长良好、增殖旺盛的间充质干细胞。
In the six basal mediums, modified DCR was the best, WPM and SH were better than GD, MS and N6 were the worse. 供试的6 种基本培养基中,改良DCR最好,WPM、SH 次之,GD 较差,MS 和N6 则不适用。
The optional medium for adventitious shoot induction from callus were MS basal medium supplemented with 2.0 mg/L Naphthalene(NAA)and 5.0 mg/L 2-Isopentyladenine(2iP),or supplemented with 0.5 mg/L NAA and 5.0 mg/L 2iP. 海滨锦葵愈伤诱导不定芽的较好培养基组合为MS+NAA2.;0mg/L+2iP5
Immature zygotic embryos of Quercus variabilis Bl. were excised and cultured on MS basal medium containing 0.25 mg/L 2,4-dichlorophenoxyace-tic acid and 0.5 mg/L 6-benzyl aminopurine. Callus was initiated from these embryos within 6 weeks. 以栓皮栎未成熟合子胚为外植体;在添加0.;25mg/L 2;4-D和0
When the callus was transfer- red to the MS basal media added to NAA(0.1 ppm)and Ze(0.25 ppm), the differentiation of shoots or roots began to occur. 将愈伤组织转移到 MS基本培养基附加 Ze(0·25ppm)及 NAA(0·lppm)培养基上,分化茎或根。
In order to improve the tissue culture technology of Siraitia grosvenorii (Swingle), stem cutting with single nod was used as explants, MS as basal medium and supplied with LFS or CPPU respectively. 摘要为给罗汉果组培技术的改进提供实验证据，以罗汉果单芽茎段作外植体，以MS为基本培养基，分别添加LFS和CPPU等生长调节剂。