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Merck
CN

Q1126

Sigma-Aldrich

Q Sepharose 快速流动

preswollen, 45-165 μm (wet), exclusion limit ~4,000,000 Da

别名:

Q Sepharose

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MDL编号:
UNSPSC代码:
47101511
NACRES:
NA.56
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表单

preswollen

质量水平

技术

RNA extraction: suitable

粒径

45-165 μm (wet)

孔径

~4,000,000 Da exclusion limit

容量

0.18-0.24 mmol Cl-/mL, packed gel

储存温度

2-8°C

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一般描述

−Ο−CH2CHOHCH2OCH2CHOHCH2N+(CH3)3

应用

Q Sepharose 用于蛋白质色谱、离子交换色谱和阴离子交换介质。Q Sepharose 已被用于研究用于植物致病真菌的自然控制的植物防御化合物。Q Sepharosehas 也被用于开发一种从土壤中提取高质量 mRNA 的有效方法,并研究大蒜(Allium sativum)的免疫调节蛋白。

外形

Preswollen 溶于 20% 乙醇

法律信息

Sepharose is a trademark of Cytiva

象形图

Flame

警示用语:

Warning

危险声明

危险分类

Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 1

闪点(°F)

100.4 - 109.4 °F - closed cup

闪点(°C)

38 - 43 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Shikimate dehydrogenase from pepper (<I>Capsicum annuum</I>) seedlings. Purification and properties.
Diaz, J., and Merino, F.
Physiologia Plantarum, 100(1), 147-152 (1997)
B Oster et al.
The Journal of general virology, 89(Pt 1), 87-96 (2007-12-20)
Here, we demonstrate that human herpesvirus 6B (HHV-6B) infection upregulates the tumour suppressor p53 and induces phosphorylation of p53 at Ser392. Interestingly, phosphorylation at the equivalent site has previously been shown to correlate with p53 tumour suppression in murine models.
Suzana M Ribeiro et al.
Peptides, 32(5), 868-874 (2010-10-20)
Antifungal proteins and peptides, essential compounds for plant defense, have been isolated from several tissues of various plants. These proteins could be used as a natural alternative to control phytopathogenic fungi. In this report a heterodimeric antifungal protein named Pa-AFP1
E G Campos et al.
International journal for parasitology, 29(5), 655-662 (1999-07-15)
Cytochrome c peroxidase oxidises hydrogen peroxide using cytochrome c as the electron donor. This enzyme is found in yeast and bacteria and has been also described in the trematodes Fasciola hepatica and Schistosoma mansoni. Using partially purified cytochrome c peroxidase
Carsten Mettel et al.
Applied and environmental microbiology, 76(17), 5995-6000 (2010-07-14)
Here, we report an efficient method for extracting high-quality mRNA from soil. Key steps in the isolation of total RNA were low-pH extraction (pH 5.0) and Q-Sepharose chromatography. The removal efficiency of humic acids was 94 to 98% for all

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