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- 文献和实验
- 技术资料
- 库存:
大量
- 供应商:
北京百奥创新科技有限公司
- 规格:
5mL;50mL;1L
乙醛活化琼脂糖凝胶4HF
产品名称:乙醛活化琼脂糖凝胶4HF英文名称:Aldehyde-activated SepFast
Product Introduction:
Aldehyde-activated agarose beads have a well-proven track record for the preparation and use of custom affinity chromatography media. Coupling biospecific ligands to aldehyde-activated agarose is a successful and well-documented technique. Aldehyde-activated SepFast media forms chemically stable secondary amine linkages with ligands containing primary amine groups through reductive amination reaction. This pre-activated agarose base matrix can be readily employed to make various custom affinity chromatography media for both small scale and large scale purification applications.

Product Properties:
There is a choice of 2 different base matrices that suit various molecules to be coupled or purified. •
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Aldehyde-activated SepFast 4 High Flow (4HF) is made of highly cross-linked 4% beaded agarose. Its large pore size is suitable for coupling or purifying large molecules. It also shows high mechanical rigidity allowing high flow throughput with reduced back pressure.
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Aldehyde-activated SepFast 6 High Flow (6HF) is made of highly cross-linked 6% beaded agarose. Its moderate pore size is suitable for coupling smaller molecules. It also shows high mechanical rigidity allowing high flow throughput with reduced back pressure.
Agarose has long been used for chromatographic separations due to its excellent hydrophilic and low non-specific-binding nature. The particles have an open pore structure with excellent mass transfer properties to various molecules. The base matrix is activated through oxidation to generate aldehyde groups. It reacts directly with the primary amine groups in molecules to be immobilized in the presence of reducing agents. Aldehyde-activated SepFast media is supplied as an aqueous suspension in 20% ethanol.
Product Series:
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文献和实验S.L. Lim, H.W. Ng, M.A. Akwiditya, C.W. Ooi, E.S. Chan, K.L. Ho, W.S. Tan, G.K. Chua, B.T. Tey, Single-step purification of recombinant hepatitis B core antigen Y132A dimer from clarified Escherichia coli feedstock using a packed bed anion exchange chromatography, Process Biochemistry, 2018, 69:208-215.
CH3 COOH,具有刺激性的液体状酸。经醋酸发酵得到食醋。在化学上,是通过乙醇的氧化,或从乙炔经由乙醛而合成。由活化酶的作用成为乙酰辅酶 A而被代谢。
(blotting);二是固定于膜上的核酸同位素标记的探针在一定的温度和离子强度下退火,即分子杂交过程。该技术是1975年英国爱丁堡大学的E.M.Southern首创的,Southern印迹杂交故因此而得名。 早期的Southern印迹是将凝胶中的DNA变性后,经毛细管的虹吸作用,转移到硝酸纤维膜上。近年来印迹方法和固定支持滤膜都有了很大的改进,印迹方法如电转法、真空转移法;滤膜则发展了尼龙膜、化学活化膜(如APT、ABM纤维素膜)等。利用Southern印迹法可进行克隆基因的酶切、图谱分析、基因
,蛋白A 琼脂糖凝胶FF 有很好的稳定性,能耐受37 度3-5 天而对柱子的性能没有影响,是分离抗体的最佳选择。疏水色谱色谱填料苯基琼脂糖凝胶FF 以及DEAE 琼脂糖凝胶FF 也场用于抗体的分离,只是特异性不如重组蛋白A 琼脂糖凝胶FF 好。纯化IgG 抗原最有效的办法是免疫亲和,具体的方法是把抗抗原的IgG 直接偶联到环氧活化琼脂糖凝胶FF 上,然后直接高pH 吸附,低pH 洗脱就可以得到需要的抗原。对于高亲和力的抗体筛选,特别是小分子的半抗原,我们建议可以把半抗原偶联到环氧活化琼脂糖凝胶FF






