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Merck
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A8312

Sigma-Aldrich

m-Aminophenylboronic acid–Agarose

aqueous suspension

동의어(들):

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

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크기 선택

5 ML
₩376,362

₩376,362

예상 입고일2025년 4월 07일세부사항

모든 사진(1)

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5 ML
₩376,362

About This Item

MDL number:
MFCD00801303
UNSPSC 코드:
12161501
PubChem Substance ID:
329770955
NACRES:
NA.32

₩376,362

예상 입고일2025년 4월 07일세부사항

양식

aqueous suspension

라벨링 범위

40-80 μmol per mL

Matrix

6% beaded agarose

기질 활성

epichlorohydrin

기질 부착

through amino to carboxyls of EDTA

기질 스페이서

9 atoms

용량

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

저장 온도

2-8°C

SMILES string

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

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관련 카테고리

일반 설명

m-Aminophenylboronic acid (m-APBA) immobilized on an agarose gel is useful in immunoglobulins capture, but also leads to non-specific interactions.[1] m-APBA is a boronate affinity matrix that is effectively used for affinity purification of monoclonal antibodies.[2]

애플리케이션

m-Aminophenylboronic acid-Agarose has been used:
  • as a component of the column for the purification of Escherichia coli TOP10F cells[3]
  • with cell lysates of various cells for detection of PARylated (Poly(ADP-ribos)ylation) proteins.[4]
  • in the affinity purification of horseradish peroxidase (HRPO)[2]
  • in the glycated human serum albumin (gHSA) purification[5]

물리적 형태

Suspension in water containing 0.002% chlorhexidine diacetate.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

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시험 성적서(COA)

Lot/Batch Number
0000269923
SLCQ0049
SLCL5912
SLCL2787
SLCJ1360

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문서 라이브러리 방문

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)
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
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
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)
Pravin K Bhatnagar et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 863(2), 235-241 (2008-02-09)
Hybrid hybridomas (quadromas) are derived by fusing at least two hybridomas, each producing a different antibody of predefined specificity. The resulting cell secretes not only the immunoglobulins of both parents but also hybrid molecules manifesting the binding characteristics of the
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