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Merck
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重要文件

M8032

Sigma-Aldrich

混合床树脂

BioReagent, for molecular biology

同義詞:

混合床树脂 氢和氢氧型

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About This Item

CAS號碼:
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.52

等級

DNA grade
for molecular biology

品質等級

產品線

BioReagent

形狀

beads

pH值

<5

異物活動

DNase, RNase, none detected

儲存溫度

room temp

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一般說明

一种自行指示混合床树脂,适用于甲酰胺、丙烯酰胺、乙二醛、PEG和尿素的去离子化。当达到交换容量时,珠子颜色从蓝色变为金色。此外,颜色指示剂接触甲酰胺后,会立即转化为金色,因此,必须通过测量电导率来检查甲酰胺的去离子化。

應用

混合床树脂适用于色谱柱或分批工艺中甲酰胺、丙烯酰胺、乙二醛、PEG和尿素的去离子化。

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

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E G Vilela et al.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 41(12), 1105-1109 (2009-01-17)
The gut barrier monitors and protects the gastrointestinal tract from challenges such as microorganisms, toxins and proteins that could act as antigens. There is evidence that gut barrier dysfunction may act as a primary disease mechanism in intestinal disorders. The
Sambrook, J., et al.
Molecular Cloning: A Laboratory Manual, 1-1 (1989)
Chih-Hsiu Lin et al.
Langmuir : the ACS journal of surfaces and colloids, 29(25), 7793-7801 (2013-05-25)
Zeta potentials of several polar protic (water, ethylene glycol, and formamide) as well as polar aprotic (dimethyl sulfoxide) liquids were measured in contact with three nonpolar surfaces using closed-cell electroosmosis. The test surfaces were chemisorbed monolayers of alkyl siloxanes, fluoroalkyl
A I Alayash
Free radical biology & medicine, 18(2), 295-301 (1995-02-01)
Chemical modifications of human or bovine hemoglobins are designed to produce proteins that can act as oxygen-carrying blood substitutes. Concerns about the redox reactivity of cell-free hemoglobin and its contribution to tissue-damaging oxygen free radicals has not been fully established.
Sina Manger et al.
Communications biology, 4(1), 234-234 (2021-02-21)
The direct study of transcription or DNA-protein-binding events, requires imaging of individual genes at molecular resolution. Electron microscopy (EM) can show local detail of the genome. However, direct visualization and analysis of specific individual genes is currently not feasible as

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