增殖培养

  • 网络Proliferation culture;enrichment culture
增殖培养增殖培养
  1. MS培养基是继代增殖培养的最适培养基;

    MS culture medium was the optimum medium for multiple culture .

  2. VA菌根真菌纯系增殖培养方法研究初报

    Studies on the methods for proliferating vesicular - arbuscular mycorrhizal fungi

  3. 结果表明:石斛兰增殖培养适宜的BA和NAA浓度都为0.5mg/L;

    The results showed that the proper concentrations of both BA and NAA for Dendrobium nobile Lindl .

  4. 以虎舌红当年生的幼茎及芽为外植体,接种于不同激素配比的MS培养基上诱导不定芽,继代并进行伸长增殖培养。

    The steins and buds of Ardisia mamillata Hance were used as explants and incubated on three kinds of 1 / 2 MS media with different hormone combinations for inducing adventitious buds .

  5. 蕙兰(Cymbidiumfaberi)原球茎增殖培养条件的研究

    Study on the culture condition of the protocorm propagation in Cymbidium faberi

  6. 结果:①加入胶质细胞源神经营养因子、白细胞介素1α增殖培养48h可见细胞分裂相。

    RESULTS ① Cell division appeared when gliacyte-derived neurotrophic factor + interleukin 1 α were added for proliferative culture for 48 hours .

  7. 继代增殖培养时,选用MS为基本培养基效果优于MS-R、GS和H培养基。

    During the shoot proliferation , we found that MS basal medium was more suitable for growth and subculture of the shoots than MS-R , Gs and H basal mediums .

  8. 彩色马蹄莲‘Parfait’不定芽诱导增殖培养条件的优化和筛选

    Optimum on induction and proliferation of adventitious buds from Zantedeschia hybrida ' Parfait ' in vitro

  9. 最适增殖培养基为MS+0.2NAA,60d后增值率达到318%;

    The optimal propagation medium was MS + 0.2 NAA and its propagation rate reached 318 % after 60 days of culturing ;

  10. 马尾松共生真菌(P.t)增殖培养条件

    The Cultural Conditions for the Proliferation of a Symbiotic Fungus ( P.t ) with Masson Pine

  11. 以麻疯树幼嫩枝条腋芽为外植体,以MS为基本培养基,附加不同浓度的激素组合(6BA与IBA)进行芽诱导和增殖培养。

    The axillary bud on young shoot of Barbados nut was used as explants , adding different concentration of plant hormone combinations ( 6-BA and IBA ) on minimal medium ( MS ), to carry out buds inducing and multiplication culture .

  12. 结果表明,DMEM/F12是一种适合表皮干细胞体外增殖培养的培养基,在此培养体系中细胞可传代至11代。

    The results showed that DMEM / F12 was a good cell culture medium for the epidermal stem cells and the epidermal stem cells can survive to the11 subculture in vitro .

  13. 直接将愈伤组织从含有2,4-D的增殖培养基转移到含有BA和NAA的植株再生培养基上培养,只能得到少量的弱苗(第1种程序)。

    Only a small number of weak plants could be regenerated when the calluses were transferred and cultured directly from a proliferation medium containing 2 , 4 D to a plant regeneration medium containing BA and NAA ( procedure 1 ) .

  14. 使用稍加修改的BM诱导和增殖培养基、分化培养基及生根培养基,用低温、常温交替培养筛选法的愈伤组织株系的存活率、分化率高于持续低温培养筛选法的。

    By use of the slight-improved BM callus induction and subculture medium . differentiation medium and rooting medium , the callus had more higher survival rate and differentiation rate under the alternative low temperature and normal temperature culture than those under the continuous low temperature culture .

  15. 核桃试管微繁增殖培养基的筛选

    Selection on the Multiplication Medium of Tube Micropropagation gation of Walnut

  16. 不同野生草莓需要不同的增殖培养基。

    The multiplication medium for each wild strawberry was different .

  17. 油松胚培养芽增殖培养基的筛选

    Selection of Basic Medium for Bud Proliferation of Embryo of Chinese Pine

  18. 采用响应面方法对唾液链球菌嗜热亚种增殖培养基进行了优化。

    Response surface method was used to optimize the MRS-based enrichment medium of S.

  19. 苹果酒酵母增殖培养基的优化

    Optimization of Medium for the Biomass Enrichment of An Apple Wine Yeast Strain

  20. 优化筛选出适合工业化生产的廉价增殖培养基和冻干复合保护剂;

    The cheap enrichment medium suited for industrial processing and freeze-drying protectant were screened .

  21. 香石竹试管苗增殖培养的研究

    Study on multiplication of test-tube shoot of caryophyllus

  22. 美国红枫种胚愈伤组织诱导、增殖培养技术研究初报

    Primary Report of Study on Induces and Proliferation of Callus from Fetus of Maple

  23. 剑叶龙血树愈伤组织的诱导及其增殖培养研究

    The Callus Induction and Proliferation of Dracaena cochinchinensis

  24. 梨矮化中间砧S5离体增殖培养基的研究

    Study on the media for proliferation in vitro of pear dwarfing inter - stock S_5

  25. 增殖培养的最适蔗糖浓度范围为8.0%~12.0%;

    The optimal concentration range of sucrose for proliferation culture was 8.0 % ﹣ 12.0 % .

  26. 对采用人工辅助授粉所得的麻竹种子,经无菌发芽增殖培养而成的实生苗无性系进行组织培养繁殖试验及生长观察。

    Tissue culture trials of the seed clones obtained from artificial pollination of Dendrocalamus latiflorus were conducted .

  27. 工艺要点有:醋酸菌的增殖培养与驯化;

    The technical points cov-ered the following aspects : the proliferation and culture and acclimatization of acetic acid bacteria ;

  28. 对香肠乳杆菌的增殖培养基及培养条件进行优化研究。

    Based on nutritional requirement for the growth of Lactobacillus farciminus , the enrichment medium of Lactobacillus farciminus was optimized .

  29. 对多花白澳山龙眼组织培养中的无菌发芽、增殖培养、幼芽伸长生长、根诱导等进行了研究。

    This paper deals with aseptic germination , proliferation culture , plumule elongation and root inducing in tissue culture of Leucadendron floridum .

  30. 增殖培养和分化培养过程中,光照培养条件较黑暗培养条件更易于愈伤组织分化,且可不同程度地缩短植株再生周期。

    During enrichment and differentiation culture , lighting culture is better than dark , and lighting culture condition can shorten the period of shoot regeneration .