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主营:分子类,蛋白类,抗体类,生化类试剂
℡ 4000-520-616
℡ 4000-520-616
Omega Bio-Tek/E.Z.N.A.® Soil DNA Kit/5-preps/D5625-00
产品编号:D5625-00
市  场 价:¥396.00
场      地:美国(厂家直采)
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:$19.80
品      牌: Omega Bio-Tek
公      司:OmegaBioTek
公司分类:
Omega Bio-Tek/E.Z.N.A.® Soil DNA Kit/5-preps/D5625-00
商品介绍

Overview

The E.Z.N.A.® Soil DNA Kit is formulated to isolate high purity cellular DNA from soil samples typically containing humic acid and other inhibitors of PCR. This kit uses a novel and proprietary method to isolate genomic DNA from a variety of environmental samples without organic extractions.

This kit has been successfully used to isolate DNA from Gram-positive and -negative bacteria, fungi, yeast, and algae that inhabit a range of samples including clay, sandy, peaty, chalky, or loamy soil samples. Isolated DNA can be used for most downstream applications, including PCR, Southern blot, and NGS analysis.

  • Reliable – Reproducible DNA purification from a variety of sample sources
  • High quality – Ready-to-use DNA eliminating PCR inhibitors using proprietary inhibitor removal technology
  • Yield – Efficient purification of DNA from even specialized samples
  • Ease of use – Contains glass beads pre-filled in 2 mL vials

Specifications

For Research Use Only. Not for use in diagnostic procedures.

FeaturesSpecifications
Starting AmountUp to 1 g
Starting MaterialSoil
YieldDependent upon sample
Elution Volume 50-100 μL
Technology HiBind® DNA Mini Column
Processing ModeManual
Throughput1-24

Kit Components

ItemAvailable Separately
HiBind® DNA Mini ColumnsView Product
2 mL Collection TubesView Product
Disruptor TubesView Product
SLX-Mlus BufferView Product
DS BufferCall for Pricing
P2 BufferView Product
cHTR ReagentView Product
XP1 Buffer---
HBC BufferView Product
DNA Wash BufferView Product
Elution BufferView Product

Protocol and Resources

Product Documentation & Literature

PROTOCOL

D5625 Soil DNA Kit

SDS

D5625 SDS

QUICK GUIDE

D5625 Quick Guide

SALES SHEET

APPLICATION NOTE

Superior Performance of Omega Bio-tek’s E.Z.N.A.® Soil DNA Kit Over CompanyM’s Soil DNA Isolation Kit for DNA Extraction from Soil Samples

Product Data

DNA purified from soil samples using E.Z.N.A.® Soil DNA Kit has higher and more consistent yield than using a leading competing product.

Figure 1. Comparison of DNA extraction method from soil samples. DNA yield determined with fluorescence-based dye quantification. 50 µL ZymoBIOMICS™ Microbial Community Standard was added to 200 mg soil samples and DNA was extracted using manufacturer’s recommended protocols. DNA was eluted in 100 µL for both manufacturers.

DNA purified from soil samples using E.Z.N.A.® Soil DNA Kit has better PCR performance than using a leading competing product.

Figure 2. Comparison of Ct values. 20 µL SYBR Green qPCR reaction. 50 µL ZymoBIOMICS™ Microbial Community Standard was added to 200 mg soil samples and DNA was extracted using manufacturer’s recommended protocols. DNA was eluted in 100 µL for both manufacturers.

E.Z.N.A.® Soil DNA Kit performs especially better for gram-positive bacteria than a leading competing product.

Figure 3. DNA yield by bacterial classes. DNA yield determined with fluorescence-based dye quantification. 0.5 mL cultured Gram-positive and Gram-negative bacteria were added to corresponding 200 mg soil samples and DNA was extracted using manufacturer’s recommended protocols. DNA was eluted in 100 µL for both manufacturers.

Publications

View Publications
  • Bao, Yun-Juan, et al. “High-Throughput Metagenomic Analysis of Petroleum-Contaminated Soil Microbiome Reveals the Versatility in Xenobiotic Aromatics Metabolism.” Journal of Environmental Sciences, vol. 56, 1 June 2017, pp. 25–35, www.sciencedirect.com/science/article/pii/S1001074216306155?casa_token=QXfnahukMoEAAAAA:H6xUoAHyfOBFs6fE1a0KcdKtiPZ53A_6EwwHMyW2uqsNhyydq52wc2CqS_UZCLFTCMB3hrpJ4yk, 10.1016/j.jes.2016.08.022. Accessed 1 June 2020.
  • Bin, Zhang, et al. “Dynamic and Distribution of Ammonia-Oxidizing Bacteria Communities during Sludge Granulation in an Anaerobic–Aerobic Sequencing Batch Reactor.” Water Research, vol. 45, no. 18, 15 Nov. 2011, pp. 6207–6216, www.sciencedirect.com/science/article/pii/S0043135411005458?casa_token=-Dxbvqho-9QAAAAA:yjdHqmoRGVk32viDMqj0l1K-hpelh9RhpMa2Z8PdTweLReQ7xB138QTS4LTnaUJIoLa_BBtHgno, 10.1016/j.watres.2011.09.026. Accessed 1 June 2020.
  • Chen, Hong, et al. “Effects of ammonia on anaerobic digestion of food waste: process performance and microbial community.” Energy & Fuels 30.7 (2016): 5749-5757.
  • Huang, Lu, et al. “Antibiotic Resistance Genes (ARGs) in Duck and Fish Production Ponds with Integrated or Non-Integrated Mode.” Chemosphere, vol. 168, Feb. 2017, pp. 1107–1114, 10.1016/j.chemosphere.2016.10.096. Accessed 9 Apr. 2020.
  • Liu, Chao, et al. “The Effects of PH and Temperature on the Acetate Production and Microbial Community Compositions by Syngas Fermentation.” Fuel, vol. 224, 15 July 2018, pp. 537–544, www.sciencedirect.com/science/article/pii/S0016236118305337?casa_token=G8sFg1-lAY8AAAAA:vc4RvQIHqKFWs7GV4IYgsFbE19hHKG64wJa-VxHX2i4bWFeht1IvIjU2sKH_DqSD7k-vhD60_yE, 10.1016/j.fuel.2018.03.125. Accessed 1 June 2020.
  • Liu, Shuang Ping, et al. “Bacterial Succession and the Dynamics of Volatile Compounds during the Fermentation of Chinese Rice Wine from Shaoxing Region.” World Journal of Microbiology and Biotechnology, vol. 31, no. 12, 22 Oct. 2015, pp. 1907–1921, 10.1007/s11274-015-1931-1. Accessed 19 May 2020.
  • Luo, Haiping, et al. “Sulfate Reduction and Microbial Community of Autotrophic Biocathode in Response to Acidity.” Process Biochemistry, vol. 54, 1 Mar. 2017, pp. 120–127, www.sciencedirect.com/science/article/pii/S1359511316304482?casa_token=UsEoVQm9jdgAAAAA:K3y18r9pkFNEGbVXRhH9NYO2kn92gUTagQO4W9ne_7__4cREpqqMoMgpy3GTE4TGCsY2GmAOpUc, 10.1016/j.procbio.2016.12.025. Accessed 1 June 2020.
  • Qin, Sijun, et al. “Forage Crops Alter Soil Bacterial and Fungal Communities in an Apple Orchard.” Acta Agriculturae Scandinavica, Section B — Soil & Plant Science, vol. 66, no. 3, Oct. 2015, pp. 229–236, 10.1080/09064710.2015.1088569. Accessed 1 June 2020.
  • Sun, Zhenli, et al. “Effects of BmCPV Infection on Silkworm Bombyx Mori Intestinal Bacteria.” PLOS ONE, vol. 11, no. 1, 8 Jan. 2016, p. e0146313, 10.1371/journal.pone.0146313. Accessed 1 June 2020.
  • Wang, Honglei, et al. “Distribution Patterns of Nitrogen Micro-Cycle Functional Genes and Their Quantitative Coupling Relationships with Nitrogen Transformation Rates in a Biotrickling Filter.” Bioresource Technology, vol. 209, 1 June 2016, pp. 100–107, www.sciencedirect.com/science/article/pii/S0960852416302656?casa_token=cLS57Ina4g8AAAAA:JNbvH3JnbxWoT94kv786jXpCfJCgxl6uJBxSB3lvU4fyXMw4NUfFrn8wCpB6M-PtoKIRRIZqzKc, 10.1016/j.biortech.2016.02.119. Accessed 1 June 2020.
  • Wang, Wen, et al. “Enhanced Fermentative Hydrogen Production from Cassava Stillage by Co-Digestion: The Effects of Different Co-Substrates.” International Journal of Hydrogen Energy, vol. 38, no. 17, 10 June 2013, pp. 6980–6988, www.sciencedirect.com/science/article/pii/S0360319913008525?casa_token=Yp5RO0rqkckAAAAA:TQ7GNvTa5EwFEgQpDmocPa28hj0Eq3LeR6esG9BZujRWKeb9Pl8UZnzwX4c64PKz2wRwp5I902E, 10.1016/j.ijhydene.2013.04.004. Accessed 1 June 2020.
  • Zhang, Bin, et al. “Microbial Population Dynamics during Sludge Granulation in an Anaerobic–Aerobic Biological Phosphorus Removal System.” Bioresource Technology, vol. 102, no. 3, 1 Feb. 2011, pp. 2474–2480, www.sciencedirect.com/science/article/pii/S0960852410018195?casa_token=xABqGAsRc00AAAAA:3-gK60wIYoio7fBqwmlb8OM2y3fRILBwWlBaemc0pz6_fZFumW9c9gC0xMmpg_gXkfTJspCIl6o, 10.1016/j.biortech.2010.11.017. Accessed 1 June 2020.
  • Zhi, Wei, et al. “Enhanced long-term nitrogen removal and its quantitative molecular mechanism in tidal flow constructed wetlands.” Environmental science & technology 49.7 (2015): 4575-4583.
  • Zhou, Min, et al. “Evolution and Distribution of Resistance Genes and Bacterial Community in Water and Biofilm of a Simulated Fish-Duck Integrated Pond with Stress.” Chemosphere, vol. 245, 1 Apr. 2020, p. 125549, www.sciencedirect.com/science/article/pii/S0045653519327894?casa_token=fHNPjCLuBx0AAAAA:AgLxYXp1gUk5K-1Y2pEEZAU8BKUOB8t_P2NU_ZgPs7QGg70yoGzdaxrL-SvewC0Wsf7VBeflGec, 10.1016/j.chemosphere.2019.125549. Accessed 1 June 2020.
  • —. “Spread of Resistance Genes from Duck Manure to Fish Intestine in Simulated Fish-Duck Pond and the Promotion of Cefotaxime and As.” Science of The Total Environment, vol. 731, 20 Aug. 2020, p. 138693, www.sciencedirect.com/science/article/pii/S0048969720322105, 10.1016/j.scitotenv.2020.138693. Accessed 1 June 2020.
Format

Miniprep

品牌介绍

欧米茄Bio-Tek


自1998年成立以来,Omega Biotek就一直在核酸纯化的前列。


自1998年成立以来,Omega Bio-tek通过提供用于临床和基础研究,生物技术和农业应用的产品,一直处于核酸纯化的最前沿。DNA和RNA提取是众多下游分析的第一步,有效而干净的核酸分离至关重要。我们的目标是提供高质量的产品,以帮助您改善工作流程。


为了满足您所有提取需求的最佳选择,我们提供了多种核酸提取化学方法,包括磁珠,硅胶膜和盐析法。这三种不同的方法可用于各种不同的套件和配置中,总共用于900多种产品。我们的第二代HiBind®二氧化硅基质具有极大的灵活性,并提供了从多种来源分离核酸的解决方案。我们的EZ核酸(EZNA®)系统采用旋转柱形式,利用了HiBind®硅胶膜,可从组织,培养的细胞,凝胶和溶液中纯化和回收DNA和RNA。我们的Mag-Bind®技术为使用磁珠分离核酸提供了灵活而可靠的方法。我们的磁珠是针对每种应用定制的,提供最佳的磁化响应时间,凝固和粘结能力。我们的产品种类繁多,从植物的RNA纯化到干血斑的DNA提取。


产品列表:



没有。

品牌

货号

名称

规格

1个

欧米茄Bio-Tek

D6922-00

EZNA®质粒最大试剂盒

2次准备

2

欧米茄Bio-Tek

M1258-00

Mag-Bind®超纯质粒DNA试剂盒

1×96

3

欧米茄Bio-Tek

D1097-00

EZ96®FastFilter质粒DNA试剂盒

1×96

4

欧米茄Bio-Tek

D2500-00

EZNA®凝胶提取试剂盒

5次准备

5

欧米茄Bio-Tek

D6538-02

EZNA®DNA探针纯化

200次准备

6

欧米茄Bio-Tek

D2500-00

EZNA®凝胶提取试剂盒

5次准备

7

欧米茄Bio-Tek

D3396-00

EZNA®组织DNA试剂盒

5次准备

8

欧米茄Bio-Tek

D1411-00

EZ96®植物DNA DS试剂盒

1×96

9

欧米茄Bio-Tek

R6950-00

EZNA®细菌RNA试剂盒

5次准备

10

欧米茄Bio-Tek

R0527-00

EZNA®RNA转运

5次准备

11

欧米茄Bio-Tek

TQ2100-00

Taq DNA聚合酶

500伙

12

欧米茄Bio-Tek

TQ2310-00

组织直接PCR试剂盒

20次准备

13

欧米茄Bio-Tek

AC10098

10 x DNA上样缓冲液

250 µL×5准备

14

欧米茄Bio-Tek

E1091

无RNase的DNase组I

50次准备

15

欧米茄Bio-Tek

AC122

糖原(20mg / mL)

500微升


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