Any culture medium that USES AGAR as the gelling agent.
任何一种用琼脂作胶凝剂的培养基。
Mushroom broth is used to replace animal tissue extract to produce mushroom culture solution and mushroom blood agar medium.
研究以平菇汤为基础成分，代替动物组织提取物，制备平菇液体培养基，平菇血琼脂培养基。
The result shows that no apparent difference was ascertained between field collections and agar-culture fruiting.
结果表明，燕麦琼脂培养的子实体与野生型子实体无明显区别。
Methods Anchorage-independent adhesion among cells was examined in soft agar culture.
方法软琼脂培养观察非锚定状态下细胞间的粘附；
The results showed that static liquid culture stimulated axillary bud development and shoot growth, but AGAR media is beneficial to induction of callus and buds formation.
试验结果表明，液体静置培养有利于腋芽发育和幼苗生长，而固体培养有利于诱导愈伤组织和芽形成。
The thin liquid culture was compared with that of the AGAR plate.
对原生质体的浅层液体培养和固体培养进行了比较。
Conclusion The scaffold made of AGAR, embryo cattle serum and antibiotics could be used to culture parenchyma cells of animals.
结论以营养琼脂、胎牛血清、抗生素按一定比例制成固体支架，可以用来培养动物软组织细胞。
Results:The CFU counting efficacy of CFU counting culture medium for Clostridium sporogenes was apparently better than those of nutrient agar medium and anaerobic bacterial agar medium(P<0.01).
结果：生孢梭菌CFU计数培养基的CFU 计数结果明显优于营养琼脂培养基和厌氧琼脂培养基（P<0.01）；
Dry culture medium was favor of regenerating plantlet, optimum AGAR content was 1.2%.
较干燥的培养基更利于小孢子胚成苗，最适的琼脂含量是1.2%。
Rheological properties of simulated plant cell suspension culture systems are studied systematically through the experiment with granulated agar that replaces plant cells.
用颗粒状琼脂代替植物细胞从实验上系统研究了模拟植物细胞悬浮培养体系的流变特性。
B5 as basic medium appended with different concentrations of sucrose, AGAR and different hormone combinations was used to optimize the culture technique for DH line in Brassica napus l.
以B5培养基为基础培养基，添加不同浓度的蔗糖、琼脂及不同激素组合进行试验，对油菜DH系的组培技术进行优化。
Firstly marine PSB is separated and purified from sea mud around Qingdao Pier by specifically culture medium and means of agar dilution.
首先使用特定的培养基，以及富集和分离技术，从青岛栈桥海域的底泥中分离出海洋光合细菌菌株；
The effects of different carbon sources, nitrogen sources, agar, natural substance, culture time and volume of culture solution on liquid culture of Inonotus obliquus were studied.
试验研究了碳源、氮源、琼脂、天然物质在桦褐孔菌菌丝体液体培养基中的配比。
The carcinogenicity of nickel compounds on human epithelial cells was identified by transforming assay, assay for culture on soft AGAR and test of tumorigenicity in nude mice.
研究几种镍化合物对培养人支气管上皮细胞的恶性转化作用及转化细胞的致癌性。
The results indicated that for culture of P. domesticum on agar plate, elution by sand washing method (140-mesh fine sand was used to replace glass beads in conventional method) had good efficacy.
结果表明，对琼脂平板上砖火丝菌培养物，采用沙洗法（以140目细沙代替常规法中的玻璃珠）洗脱，效果较好。
METHODS Sabourand′s agar culture medium was used to culture fungi, ID identification strip was employed to identify the fungi and drug sensitive test was performed by disk diffusion test.
方法沙保弱培养基培养标本，用ID真菌鉴定板条进行鉴定分型，纸片扩散法进行药敏实验。
Results of AGAR culture and soil culture indicated that the amounts of plaque iron on rice cultivars with different oxidizing power of roots were different.
采用琼脂培养和土壤培养试验研究了根系氧化能力不同的水稻品种磷、锌的营养状况。
There are 5 types of cellular morphology of colonies in agar culture of mouse granulocyte macrophage progenitors(GM-CFC).
本文通过琼脂培养小鼠骨髓GM-CFC，经过原位染色，在高倍显微镜下动态观察了集落的细胞形态学。
Methods Compounded one kind of trisaccharide iron urea indol culture medium and the trisaccharide iron AGAR has carried on the contrast experiment with the national standard method in voluntarily.
方法自行配制了一种三糖铁尿素靛基质培养基，并与国家标准方法中三糖铁琼脂进行了对比试验。
Semisolid agar culture to observe the effects of different concentration of drug-containing serum and Rubus parvifolius saponins on K562 cell colony formation;
半固体琼脂培养观察不同浓度的含药血清和茅莓总皂苷对K562细胞株集落生长的影响；
When scientists are trying to grow a culture, AGAR is the growth medium of choice.
就在科学家们试图培植一种培养基时，琼脂成了他们的精选品。
The quick tubercle mycobacillus culture medium has tryptone, sodium gluconate, pyritinol hydrochloride, water solution of malachite green, glycerin, agar, calf blood and other components.
所述培养基的主要成分是胰蛋白胨、葡萄 酸钠、盐酸吡咯醇、孔雀绿水溶液、甘油、琼脂、小牛血清等。
It is showed that the cell clone-forming rat was 31. 2%. The immortalized human fetal hepatocytes had a normal karyotype and were not able to grow in soft AGAR culture.
结果显示永生化胚胎肝细胞克隆形成率为31.2%，染色体核型分析表明细胞核型无明显异常，软琼脂集落形成试验表明细胞在软琼脂中不能生长。
It is showed that the cell clone-forming rat was 31. 2%. The immortalized human fetal hepatocytes had a normal karyotype and were not able to grow in soft AGAR culture.
结果显示永生化胚胎肝细胞克隆形成率为31.2%，染色体核型分析表明细胞核型无明显异常，软琼脂集落形成试验表明细胞在软琼脂中不能生长。
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