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EnzymoPure™,suitable for mass spectrometry (MS),Recombinant,≥99%(HPLC),≥50 U/μg protein Recombinant,질량 분석법(MS)에 적합함,EnzymoPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Avoid repeated freezing and thawing Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
IdeS (IgG-specific degrading enzyme) is an engineered protease recombinantly expressed in Escherichia coli. It specifically cleaves immunoglobulin G at a single recognition site below the hinge region to generate homogeneous F(ab´)₂ and Fc fragments. Both IdeS and IdeZ proteases efficiently cleave human IgG1, IgG2, IgG3, IgG4, monkey, sheep, rabbit, humanized and chimeric IgG antibodies, as well as Fc fusion proteins. However, only IdeZ protease cleaves mouse IgG2a and IgG3. Reconstitution: Reconstitute with 40 μL of ultrapure water. Digestion Buffer: 10× buffer containing 50 mM PBS, 150 mM NaCl (pH 6.6). pH Range: Optimal activity at pH 6–8. Application: · IdeS protease is an IgG-specific protease that generates homogeneous F(ab´)₂ and Fc fragments. · Recommended Digestion SOP: · Take 10 μL of mAb sample at 10 μg/μL; · Add 5 μL of 10× digestion buffer and 31 μL of ultrapure water, mix to a total reaction volume of 50 μL; · Add 4 μL of rIdeS protease at 0.5 μg/μL; · Incubate at 37 °C for 30 minutes.
Comprehensive hazard, handling, storage, and regulatory compliance document.
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