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Merck
CN

Y1251

Millipore

酵母氮源基础,不含氨基酸和硫酸铵

NutriSelect® Basic, suitable for microbiology

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UNSPSC代码:
41171606
NACRES:
NA.85

无菌性

non-sterile

质量水平

形式

powder

包装

poly bottle of 1 kg
poly bottle of 500 g

制造商/商品名称

NutriSelect® Basic

溶解性

water: soluble 67 mg/mL

应用

clinical testing
food and beverages
life science and biopharma

microbiology

适用性

Candida spp.
Pichia spp.
Saccharomyces spp.
Zygosaccharomyces spp.
molds
yeasts

一般描述

酵母氮源基础/Yeast Nitrogen Base(不含氨基酸和硫酸铵)推荐用于根据酵母的碳源和氮源需求进行菌种分类。培养基包含酵母生长必需的所有营养素,但不含氨基酸、组氨酸、甲硫氨酸和色氨酸,以及硫酸铵。根据《临床微生物学手册》所述,培养时还需要添加氮源和碳源。

应用

酵母氮源基础/YNB(不含氨基酸和硫酸铵)用于通过碳源和氮源利用对酵母进行分类。除氨基酸、氮源和碳水化合物之外,包含酵母生长的所有必需营养素。需要添加氮源和碳源。

组分

成分
生物素,2 μg/L
泛酸钙,400 μg/L
叶酸,2 μg/L
烟酸, 400 μg/L
对氨基苯甲酸,200 μg/L
盐酸吡哆醇,400 μg/L
核黄素,200 μg/L
盐酸硫胺素,400 μg/L
肌醇,2 mg/L
硼酸,500 μg/L
硫酸铜,40 μg/L
碘化钾,100 μg/L
氯化铁,200 μg/L
硫酸锰,400 μg/L
钼酸钠,200 μg/L
硫酸锌,400 μg/L
磷酸二氢钾,1 g/L
硫酸镁,0.5 g/L
氯化钠,0.1 g/L
氯化钙,0.1 g/L

制备说明

  • 将1.7 g不含氨基酸和硫酸铵的酵母氮源混悬于冷却的100 mL蒸馏水中,制得10×储备溶液。包含所需的氮和碳源。
  • 必要时可加温溶解,然后过滤灭菌。
  • 将10×储备溶液储存于2-8°C。使用时,在无菌条件下用无菌蒸馏水1:10稀释。

附注

我们现提供两种类型的培养基:GranuCult®优质颗粒状培养基和NutriSelect®高性价比粉末状培养基,满足用户不同层次的需求。
商标后的品级称号basic(基础)、plus(加强)或prime(特级)代表产品的不同质控水平,从基础的质控到标准质控加强版到全面合规的特级质控水平。

法律信息

GRANUCULT is a registered trademark of Merck KGaA, Darmstadt, Germany
NutriSelect is a registered trademark of Merck KGaA, Darmstadt, Germany

仅试剂盒组分

产品编号
说明

  • KH2PO4 1 g/L

  • MgSO4 .5 g/L

  • NaCl .1 g/L

  • CaCl2 .1 g/L

  • Inositol 2 mg/L

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

动植物来源培养基

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

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在文件库中查找您最近购买产品的文档。

访问文档库

Michael Mülleder et al.
Cell, 167(2), 553-565 (2016-10-04)
Genome-metabolism interactions enable cell growth. To probe the extent of these interactions and delineate their functional contributions, we quantified the Saccharomyces amino acid metabolome and its response to systematic gene deletion. Over one-third of coding genes, in particular those important for chromatin dynamics
Sviatlana Shashkova et al.
Bio-protocol, 8(2), e2710-e2710 (2018-02-13)
Single-molecule fluorescence microscopy enables unrivaled sub-cellular quantitation of genomically encoded fusions of native proteins with fluorescent protein reporters. Fluorescent proteins must undergo in vivo maturation after expression before they become photoactive. Maturation effects must be quantified during single-molecule analysis. Here
Yuping Lin et al.
Biotechnology for biofuels, 7(1), 126-126 (2014-12-02)
Saccharomyces cerevisiae, a key organism used for the manufacture of renewable fuels and chemicals, has been engineered to utilize non-native sugars derived from plant cell walls, such as cellobiose and xylose. However, the rates and efficiencies of these non-native sugar
Ligia Acosta-Sampson et al.
The Journal of biological chemistry, 292(48), 19610-19627 (2017-10-04)
Targeting of most integral membrane proteins to the endoplasmic reticulum is controlled by the signal recognition particle, which recognizes a hydrophobic signal sequence near the protein N terminus. Proper folding of these proteins is monitored by the unfolded protein response
Xin Li et al.
eLife, 4 (2015-02-04)
Sustainable biofuel production from renewable biomass will require the efficient and complete use of all abundant sugars in the plant cell wall. Using the cellulolytic fungus Neurospora crassa as a model, we identified a xylodextrin transport and consumption pathway required

商品

Traditional methods are based morphology, staining methods, enzyme reactions (metabolism) and diverse media.

实验方案

Yeast culture techniques: Model systems for eukaryotic studies with liquid media or agar plate growth.

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