Protein L resin in HiScreen™ columns for affinity capture of antibody Fabs, bispecifics, and other variants containing a kappa light chain From1,410.00 USD HiScreen™ MabSelect™ VL 17542015 1,410.00 USD Min qty: 1 Selling fast
本品Protein L 4FF Chromatography Column,1mL是一种装填了Protein L Agarose Resin 4FF的中压预装柱,规格5mL,预装柱具有标准接口,可以适配商品化的各类中压色谱系统,如?KTA 等,方便客户操作。 产品性质 基质(Matrix) 高度交联的4%琼脂糖微球 配体(Ligand) ...
本品rProtein L 4FF Chromatography Column,5 mL是一种装填了rProtein L Agarose Resin 4FF的中压预装柱,规格5 mL,预装柱具有标准接口,可以适配商品化的各类中压色谱系统,如ÄKTA 等,方便客户操作。 产品信息 货号 36416ES08 / 36416ES25 规格 5 mL /5×5 mL 产品性质 基质(Matrix) 高度交联的4%琼...
Protein A、G、L 4FF Chromatography Column Protein A/G MagBeads (IP Grade) 平均粒径d50V 45-165µm 45-165µm 45-165µm 1μm 配基 重组蛋白 重组耐碱蛋白 重组耐碱蛋白 重组Protein A/G 载量 Protein A > 40mg人IgG/mL Protein G > 30mg人IgG/mL Protein A/G > 20...
Protein A Sepharose Column;蛋白A琼脂糖凝胶柱 Columns with Reusable Protein A conjugated Sepharose beads with ≥16 mg/ml binding capacity & 2.07 ml/min flow rate for antibody purification from multiple sources Protein A-Sepharose Columns are prepared by covalently coupling recombinant Protein A to 6%...
In detail, the TMT-labeled peptide samples were resuspended in 100 μl of 20 mM ammonium formate pH 10 (Buffer A). The total volume of each sample was injected onto an Acquity UPLC BEH C18 column (2.1-mm inner diameter × 150 mm; 1.7-μm particle size) on an Acquity ...
The filtered solution was loaded onto a cobalt affinity resin column (Takara). His tagged proteins were eluted with 150 mM imidazole and concentrated in storage buffer (25 mM HEPES pH 7.4, 300 mM NaCl, 5 mM DTT, and 10% glycerol) using Amicon 10 kDa cutoff filters (Merck). Produced ...
Pass the supernatant (clarified cytosol containing the RhoA/GST-GDI complex) through a 1 -ml column of glutathione-Sepharose at 4° at a rate of <1 ml/min to allow time for binding. Wash the resin with 20 ml of solution I containing 10 μM GDP and elute the RhoA with ten 1-ml ali...
Mouse organ samples were loaded onto a 15-cm reverse-phase column packed with 3-μm resin, separated over 320 min of gradient time, and analyzed on an LTQ Orbitrap mass spectrometer using collision-induced dissociation fragmentation. MS data were analyzed using the MaxQuant software environment (...
When their multiplication reached the logarithmic growth stage, the parasites were purified from blood by chromatography on a DEAE (diethylaminoethyl) cellulose column, as previously described [75]. After elution, the parasites were washed three times in sterile phosphate-buffered saline (PBS) solution...