Merck
CN

L3522

Sigma-Aldrich

LB肉汤(Miller)

Highly-referenced nutrient-rich microbial growth powder medium, suitable for regular E.coli culture

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别名:
Luria肉汤, Miller LB肉汤
NACRES:
NA.85

等级

for molecular biology

质量水平

描述

Miller′s Modification, 10 g/L NaCl

无菌性

non-sterile

形式

powder

组成

NaCl, 10 g/L
Tryptone, 10 g/L
Yeast Extract, 5 g/L

pH值(酸碱度)

6.8-7.2(2.5% solution)

application(s)

food and beverages

储存温度

room temp

适用性

nonselective for Escherichia coli
nonselective for coliforms

一般描述

Miller LB是一种高被引用的微生物生长培养基,用于培养 大肠杆菌。 这种营养丰富的微生物肉汤含有多肽、氨基酸、水溶性维生素和碳水化合物。

应用

LB液体培养基(Miller)用作大肠杆菌恶臭假单胞菌KT2440、副溶血性弧菌,以及用于分离芽孢杆菌的土壤样本的培养基。
适用于大肠杆菌菌株的非选择性培养,用于克隆、DNA质粒生产和重组蛋白生产。当加入适当的抗生素时,也适合选择性培养。

生化/生理作用

Luria肉汤被用于大肠杆菌(Escherichia coli)的维持和繁殖。 大肠杆菌在Luria肉汤中生长得更快,因为胰蛋白胨和酵母为其提供了必需的生长因子,从而无需大肠杆菌自身进行合成。 由于含有NaCl成分,Luria肉汤还含有转运和渗透平衡所必需的电解质

特点和优势

Miller LB粉末:
  • 包装尺寸更大,易于扩大规模
  • 液体的廉价替代品
  • 标准配方

制备说明

1.取25 g溶于1L蒸馏水中。
2.121 °C下高压灭菌15分钟。
制备Luria、Adams和Ting培养基(也称为LC液体培养基):高压灭菌后,无菌加入25 mL无菌0.1M氯化钙。

重悬

搅拌,使25g粉末悬浮于1L水中。 在121℃高压灭菌15分钟。 先冷却再添加其他成分,如抗生素(如果需要)。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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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示例

T1503
货号
-
25G
包装规格/数量

其它示例:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

输入内容 1.000309185)

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索取COA

  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What are the differences among the Luria, Lennox and Miller LB formulations?

    LB, (originally termed lysogeny broth) was initially composed of tryptone, yeast extract, NaCl and glucose.  Soon after, the glucose was omitted (Miller's version), and later the NaCl content lowered by half (Lennox's version).  For some applications, even lower salt is required (Luria's low salt version). 

  6. What is the difference among the LB - Miller products?

    LB - Miller is available in many types to suit your needs.  The different product formats include powder and liquid form.  The powder form is also available with agar for easy LB-agar plate preparation.L2542 (LB Miller liquid)L3522 (LB Miller powder)L3147 (LB Miller powder with agar)

  7. Which bacterial culture medium is the best choice for my application?

    Each of the broths will likely grow E. coli very well, but there are still general guidelines for choosing a broth when you are working without a protocol. Generally:LB - Miller and LB - Lennox are used for E. coli growth and maintanence, DNA plasmid production and protein production.  The Lennox formulation has a lower salt content required for some salt-sensitive selection antibiotics.LB - Luria low salt is used for special applications where the E. coli growth or other constraints require the lowest possible salt content.Terrific Broth is used for higher yield protein production and high yield DNA plasmid production, because of the faster growth of the E. coli in this medium.SOB is used for protein production, DNA plasmid production and the generation of high-efficiency competent cells.SOC is used for initial growth of competent cells and the transformation procedure.

  8. Will adding magnesium to the culture medium increase cell density?

    In microbial broth formulations that do not already contain magnesium, the addition of 10-20 mM MgCl2 or MgSO4 may increase cell densities.  You may need to also increase the shaking speed of the incubator. 

  9. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Transcriptional profiling of Vibrio parahaemolyticus exsA reveals a complex activation network for type III secretion
Liu AC and Thomas NA
Frontiers in Microbiology, 6, 1089-1089 (2015)
Atlas, R. M., L.C. Parks
Handbook of Microbiological Media (1993)
Single-cell bacteria growth monitoring by automated DEP-facilitated image analysis
Peitz I and van Leeuwen R
Lab on a chip, 10(21), 2944-2951 (2010)
Selecting lipopeptide-producing, Fusarium-suppressing Bacillus spp.: Metabolomic and genomic probing of Bacillus velezensis NWUMFkBS10. 5
Adeniji A, et al.
MicrobiologyOpen, e742-e742 (2018)
Demeng Tan et al.
Microorganisms, 8(3) (2020-03-12)
Phage therapy is a potential and promising avenue for controlling the emergence and spread of multidrug-resistant (MDR) Klebsiella pneumoniae, however, the rapid development of anti-phage resistance has been identified as an obstacle to the development of phage therapy. Little is

商品

The development of genetic engineering and cloning has opened many possibilities of expression and isolation of heterologous proteins for research purposes. Considerable advances in technology have enabled expression and isolation of recombinant proteins in large scale.

Whole transcriptome amplification (WTA) is a method often used to amplify small quantities of reverse transcribed RNA, or degraded RNA for direct use in Next-Generation Sequencing (NGS) workflows. Discover our SeqPlex™-I WTA library preparation kit for producing libraries that are ready for direct input onto Illumina® NGS flow cells.

基因工程和克隆的发展为研究领域开辟了表达和分离异源蛋白质的许多可能性。技术上巨大进步使得能够大规模表达和分离重组蛋白。

实验方案

General protocols for growth of competent cells in microbial medium.

在从小型培养到发酵级的不同规模下培养大肠杆菌。包括了用于启动起始培养物、悬浮细胞、单一培养物和平板噬菌体M13的实验方案。

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