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naphthaleneacetic相关的网络例句

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The greatest efficiency in Agrobacterium-mediated transformation of lettuce cotyledons(2~3 days-old) was obtained by 10-time dilution of Agrobacterium cells, 15-min inoculation time,1-day pre-culture,4-day co-culture and without AS using the MS(Murashige and Skoog\'s,1962) medium supplemented with 0.2 mg/L 6-benzylaminopurine,0.1 mg/Lα-naphthaleneacetic acid,100 mg/L Kan and 500 mg/L Carb,.

在农杆菌介导的皱叶生菜子叶(2~3 day苗龄)转化试验中,采用含BA 0.2mg/L,NAA 0.1 mg/L,Kan 100 mg/L,Carb 500 mg/L的MS培养基,最优的转化条件为农杆菌稀释倍数为10倍,预培养时间为1 day,共培养时间为4 day,浸染时间为15 min,不添加乙酰丁香酮。

Pedicel axillary buds were cultured on Murashige and Skoog's basal medium with combi-nations of 6-benzylaminopurine (2-3 mgIL) and α-naphthaleneacetic acid (0.1-0.5 mg/L).

在不含其他有机添加物,只添加BA (3 mg/L)+ NAA (0.1 mg/L)的MS培养基中,原球茎诱导效率达80%。

When the protoplast-derived calli were transferred into the MS solid medium added with 2.0mg/L benzylamino-purine and 0.4mg/L naphthaleneacetic acid and cultivated in the codition of low illumination, after which the adventitious shoots were induced, then we could obtain numerous plantlets and could transplant them survival to pots in the greenhouse.

当将原生质体分裂形成的愈伤组织转移到附加2.0mg/L6-苄氨基嘌呤和0.4mg/L萘乙酸的MS固体培养基上,并在低光照条件下培养后,从愈伤组织上分化出了不定芽,进而发展成小植株,并移栽成活。

Effects of ABT rooting powder No.1 (ABT1),α-Naphthaleneacetic acid and Indolebutyric acid on the rooting rates, biomass and taxol contents of Taxus chinensis var. mairei cuttings were studied in this experiment.

以清水处理为对照,使用不同激素(ABT1号生根粉、NAA、IBA)处理南方红豆杉插穗,从而研究不同激素处理对南方红豆杉扦插苗生根率、生物量及紫杉醇含量的影响。

Calli were induced at a high frequency of 76.4±3.2% from petiole explants excised from two-month-old plants on Murashige and Skoog medium supplemented with 5.37 μMα-naphthaleneacetic acid and 4.44 μM 6-benzyladenine.

采用2个月苗龄植株的幼叶柄为外植体,接种於附加5.37μMNAA和4.44μMBAMS培养基,愈伤组织诱导频率高达76.4±3.2%。

No callus could be induced from leaf or petiole explants of varieties F30 and Ⅱ cultured on MS medium if supplemented alone with 6-bezyladenine (6-BA) or thidiazuron, or kinetin. However, the calli were induced on MS medium containing 2.0 mg L-1 6-BA and 0.5 mg L-1 NAA (α-naphthaleneacetic acid), and the calli derived from petioles of variety Ⅱ could produce redifferentiated shoots, but of variety F30 could not. The later could only produce shoots directly from the base of the petioles.

将品种F30和Ⅱ的叶片和带叶叶柄接种到含不同浓度单一细胞分裂素(6-BA、TDZ、KT)的MS培养基上培养,均未能诱导出愈伤组织,而在含2.0mgL-1 6-BA+0.5mgL-1 NAA的培养基上可以诱导出愈伤组织,且由品种Ⅱ叶柄诱导产生的愈伤组织可再分化出芽,品种F30诱导的愈伤组织却不能分化,但在其叶柄基部可直接出芽。

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