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Merck
CN

A8312

Sigma-Aldrich

m-氨基苯基硼酸-琼脂糖

aqueous suspension

别名:

(3-aminophenyl)boronic acid-Agarose, 3-Aminophenylboronic acid–Agarose, m-APBA-Agarose, m-Aminophenylboronic acid resin

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About This Item

MDL编号:
UNSPSC代码:
12161501
PubChem化学物质编号:
NACRES:
NA.32

表单

aqueous suspension

质量水平

标记范围

40-80 μmol per mL

基质

6% beaded agarose

基质活化

epichlorohydrin

基质附着

through amino to carboxyls of EDTA

基质隔离区

9 atoms

容量

≥8 mg/mL binding capacity (peroxidase Type VI)

储存温度

2-8°C

SMILES字符串

[X]Nc1cc(ccc1)B(O)O

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相关类别

一般描述

固定在琼脂糖凝胶上的m-氨基苯硼酸(m-APBA)可用于捕获免疫球蛋白,但也适用于非特异性作用分子。m-APBA是一种硼酸亲和基质,主要用于高效亲和纯化单克隆抗体。

应用

m-氨基苯硼酸琼脂糖已用于:
  • 作为色谱柱成分,用于纯化大肠杆菌TOP10F细胞
  • 与各种细胞的裂解液混合,用于检测聚ADP核糖基化(PARylated)蛋白。
  • 辣根过氧化物酶(HRPO)的亲和纯化
  • 糖化人血清白蛋白(gHSA)纯化

外形

悬浮于含0.002%醋酸氯己定的水中。

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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T A Myöhänen et al.
The Biochemical journal, 197(3), 683-688 (1981-09-01)
The synthesis of 3-nitro-4-(6-aminohexylamido)phenylboronic acid is described. The properties of two novel forms of immobilized phenylboronate agarose adsorbents [m-aminophenylboronic acid-Matrex Gel and 3-nitro-4-(6-aminohexylamido)phenylboronic acid-Sepharose CL-6B] were investigated. Both gels bind and selectively retard the glycoprotein alpha-glucosidase from yeast. The retardation
Monika Kijewska et al.
Molecules (Basel, Switzerland), 25(3) (2020-02-14)
We report herein a novel ChemMatrix® Rink resin functionalised with two phenylboronate (PhB) moieties linked on the N-α and N-ε amino functions of a lysine residue to specifically capture deoxyfructosylated peptides, compared to differently glycosylated peptides in complex mixtures. The
RUNX poly (ADP-ribosyl) ation and BLM interaction facilitate the Fanconi anemia pathway of DNA repair
Tay L S, et al.
Testing, 24(7), 1747-1755 (2018)
Construction and optimization of a CC49-Based scFv-beta-lactamase fusion protein for ADEPT
Roberge M, et al.
Protein engineering, design & selection : PEDS, 19(4), 141-145 (2006)
Qian Chen et al.
The EMBO journal, 40(2), e104542-e104542 (2020-12-03)
Optimal DNA damage response is associated with ADP-ribosylation of histones. However, the underlying molecular mechanism of DNA damage-induced histone ADP-ribosylation remains elusive. Herein, using unbiased mass spectrometry, we identify that glutamate residue 141 (E141) of variant histone H2AX is ADP-ribosylated

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