MS culture medium

MS culture medium was the optimum medium for multiple culture .

MS培养基是继代增殖培养的最适培养基；

Effects of Different High Temperature Treatments on pH Value of MS Culture Medium

高温不同处理对MS培养基pH值的影响

The transformants were selected on the MS culture medium containing Kanamycin .

叶片进行遗传转化。在含卡那霉素的MS分化培养基上选择转化体和植株再生，转化植株可在含卡那霉素的生根培养基中生根。

Append different concentration salicylic acid to MS culture medium , SA can enhance the total flavonoids content in culture Gynostemma .

在MS培养基中附加不同浓度的SA后，使用外源的SA能够提高绞股蓝组织培养苗的总黄酮含量。

Tests were made on current-growth branches of 5-year-old Taxus media on MS culture medium with different consistency of NAA or 6-BA .

以5a生曼地亚红豆杉当年生枝条的带芽茎段为外植体，用MS作基本培养基，进行NAA和6-BA的单因素浓度梯度组织培养试验。

When larva embryo segregation culture after hybridisations the addition of MS culture medium are 0.01mg/1 NAA . This culture medium is the best .

在杂交后幼胚离体培养时，以MS培养基加0.01mg／l的NAA为最佳。

The extracts of several Chinese medicinal herbs were separately added into the improved MS culture medium to study the effects on the growth of grape stem - apex in vitro .

在改良MS培养基中加入几种中草药剂处理，研究对葡萄茎尖组培苗生长势的影响。

The auxin of culture medium for inducing callus , bud , root ; inoculating method , transplanting were investigated through inoculating 3 kinds of Cyclamen into MS culture medium containing different auxin .

通过对仙客来3个品种接入到不同激素的MS培养基中，对诱导产生愈伤组织、芽、根的培养基的激素，接种方法，假植等进行了较深入地研究。

Methods The seedlings were tested as the explants and cultured on 1 / 2 MS culture medium with extract from banana at the concentration of 20 % and different portions of three kinds of rare earth elements .

方法通过正交试验，以石斛小苗为外植体，培养在附加了3种不同稀土元素组合的1/2MS+20%的香蕉提取物的培养基上进行培养。

Nine excellent Cunninghamia lanceolata clones with high genetic gains were selectively used to make the tissue culture and induction budding experiment and the results revealed that the MS culture medium was suitable for the tissue culture of C.

选用9个高遗传增益的杉木优良无性系进行组织培养、诱导发芽试验，结果表明：MS培养基适用于杉木组织培养；

Study the effect of hormone and their combination to callus continue culture , when the callus was cultured on MS culture medium with 6-BA 1.0 ~ 2.0mg/Land lower concentration of ZT 、 KT , then embryogenic callus appeared .

胚性愈伤组织诱导过程中，在MS培养基中添加1.0～2.0mg/L的6-BA能诱导出胚性愈伤组织，低浓度的ZT、KT可起到促进胚性愈伤组织形成的作用。

1 / 2 MS liquid culture medium is suited to be sonic solution ;

1/2MS液体培养基适宜作为超声溶液；

But Virginia Creeper are living in takes 1 / 2 MS as the fundamental culture medium to grow better .

而五叶爬山虎则在以1／2MS为基本培养基中生长较好。

This experiment is that MS is the capital culture medium adding different kinds and different concentration of CTK and IAA carrying through the experience .

MS附加不同种类、不同浓度的细胞分裂素和生长素，进行正交设计。

The effects of different plant hormones on the alfalfa callus induction were investigated with MS as the basic culture medium . Consequently , the best culture medium for callus induction was selected out .

以MS为基本培养基，研究不同激素对紫花苜蓿2号愈伤组织的诱导效果，筛选出最佳诱导愈伤组织培养基；

The results show that the basic culture medium is that of 1 / 2 MS , the second culture medium is that of 1 / 3 MS and the fitting inoculation time is March and April .

结果表明：基本培养基以1/2MS较好，继代培养基以1/3MS为佳，最佳接种时间为3月初至4月上旬。

The experiments were used the stem with growing point of double flower Hemerocallis fulva as test plant . The MS and 1 / 2 MS as culture medium were each added different concentration 2,4-D , 6-BA and NAA .

试验以重瓣大花萱草带生长点的茎段为试材，以MS与1/2MS为基本培养基，分别添加不同浓度的2,4-D，6-BA，NAA。