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Merck
CN
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主要文件

W1754

Sigma-Aldrich

PCR Reagent, suitable for PCR

别名:

H2O

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10 G
¥1,590.46
100 G
¥9,752.37

¥1,590.46


国内现货,预计发货时间2025年4月07日详情



选择尺寸

变更视图
10 G
¥1,590.46
100 G
¥9,752.37

About This Item

线性分子式:
H2O
CAS号:
分子量:
18.02
Beilstein:
2050024
EC 号:
MDL编号:
UNSPSC代码:
12191602
PubChem化学物质编号:
NACRES:
NA.25

¥1,590.46


国内现货,预计发货时间2025年4月07日详情


产品名称

水, PCR Reagent

蒸汽密度

<1 (vs air)

蒸汽压

3 mmHg

无菌性

sterile-filtered

表单

liquid

包装

vial of 1.5 mL

技术

PCR: suitable

折射率

n20/D 1.34 (lit.)

pH值(酸碱度)

5-7

沸点

100 °C (lit.)

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D-(+)-Glucose suitable for mouse embryo cell culture, &#8805;99.5% (GC)

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D-(+)-Glucose powder, BioReagent, suitable for cell culture, suitable for insect cell culture, suitable for plant cell culture, &#8805;99.5%

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D-(+)-Glucose Hybri-Max&#8482;, powder, BioReagent, suitable for hybridoma

G5146

D-(+)-Glucose

D-(+)-Glucose &#8805;99.5% (GC), BioXtra

G7528

D-(+)-Glucose

technique(s)

cell culture | embryo: suitable

technique(s)

cell culture | insect: suitable, cell culture | mammalian: suitable, cell culture | plant: suitable

technique(s)

cell culture | hybridoma: suitable

technique(s)

gas chromatography (GC): suitable

solubility

H2O: 2g + 15 mL, clear, colorless

solubility

H2O: 2g + 15 mL (Tested)

solubility

H2O: 2g + 15 mL (Tested)

solubility

H2O: 1 M

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

form

powder

form

powder

form

powder

form

powder

mp

150-152 °C (lit.)

mp

150-152 °C (lit.)

mp

150-152 °C (lit.)

mp

150-152 °C (lit.)

一般描述

对 PCR 级水进行无菌过滤。它不含核酸外切酶(dna 酶、rna 酶)和核酸内切酶(切口酶),也不含核酸污染。

应用

水已用于:

  • 作为反应混合物的组分和微流控RT-qPCR的稀释剂[1]
  • 作为反应混合物的组分,以扩增真菌(杂色云芝)DNA的产物[2]
  • 作为稀释剂和反应混合物的组分,以扩增cDNA[3]
  • 水已用于在聚合酶链式反应 (PCR) 中补充样品的最终体积[3]

适用性

适用于聚合酶链式反应 (PCR)

其他说明

便于将水产品规格与 水规格表进行比较

储存分类代码

12 - Non Combustible Liquids

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

  • 技术规格说明书

  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

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    访问文档库

    J Loeffler et al.
    Journal of clinical microbiology, 37(4), 1200-1202 (1999-03-13)
    Successful in vitro amplification of fungal DNA in clinical specimens has been reported recently. In a collaboration among five European centers, the frequency and risk of contamination due to airborne spore inoculation or carryover contamination in fungal PCR were analyzed.
    Francine Marciano-Cabral et al.
    Applied and environmental microbiology, 69(10), 5864-5869 (2003-10-09)
    The free-living amoeboflagellate Naegleria fowleri is the causative agent of primary amoebic meningoencephalitis (PAM), a rapidly fatal disease of the central nervous system. In the United States, the disease is generally acquired while swimming and diving in freshwater lakes and
    N Wellinghausen et al.
    Applied and environmental microbiology, 67(9), 3985-3993 (2001-08-30)
    Contamination of hospital water systems with legionellae is a well-known cause of nosocomial legionellosis. We describe a new real-time LightCycler PCR assay for quantitative determination of legionellae in potable water samples. Primers that amplify both a 386-bp fragment of the
    Multiplex PCR for rapid detection of genes encoding acquired metallo-beta-lactamases.
    Matthew J Ellington et al.
    The Journal of antimicrobial chemotherapy, 59(2), 321-322 (2006-12-23)
    Incidence and survival of non-O157 verocytotoxigenic Escherichia coli in soil
    Bolton DJ, et al.
    Journal of Applied Microbiology, 111(2), 484-490 (2011)

    商品

    Small interfering RNAs (siRNAs) are powerful tools for gene expression knockdown, widely used in molecular biology.

    实验方案

    Hot start dNTP protocol enhances specificity in PCR by blocking DNA polymerase nucleotide incorporation during PCR.

    Protocol describes amplification of DNA through quantitative PCR with SYBR Green. Consistent batch-to-batch performance can be achieved with large numbers of PCR reactions.

    Protocol for high fidelity amplification of long PCR fragments up to 22kb from complex DNA mixtures and up to 40kb from simple DNA mixtures. AccuTaq LA.

    Reverse transcription (RT) is the process of converting RNA to cDNA using a reverse transcriptase enzyme and dNTPs.

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