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关键词:'369-34-6'
显示 1-10 #N/A 1355 条结果 关于 "369-34-6" 范围 网站内容
Purification of Histidine-Tagged Recombinant Proteins Using Ni Sepharose® High Performance
Ni Sepharose High Performance consists of highly cross-linked 6% agarose beads (34 µm) to which a chelating group has been immobilized and subsequently charged with Ni2+ ions.
Performing a Separation with IgG Sepharose 6 Fast Flow
Perform a separation with IgG Sepharose 6 Fast Flow from Cytiva, an Affinity Chromatography product for purification of recombinant fusion proteins containing a protein A tail.
Ni Sepharose 6 Fast Flow for Protein Purification
Ni Sepharose 6 Fast Flow purifies histidine-tagged proteins efficiently, offering high cross-linked agarose beads with Ni2+ ions.
Oligonucleotide Standard 6 Mix LC-UV Analysis
Chromolith® RP-18e columns optimize Oligo Standard 6 separation with varied flow rates and ion-pairing reagent evaluation.
Enzymatic Activity of Glucose-6-Phosphatase [EC 3.1.3.9]
To measure glucose-6-phosphatase activity, the Taussky-Shorr method is used. This method is a spectrophotometric stop-rate determination assay that is measured at 660 nm.
Top 6 "Things to Do" for the Use of Pure Water Machines
Top 6 "Things to Do" for the Use of Pure Water Machines
Enzymatic Assay of Glucose-6-Phosphate Dehydrogenase (EC 1.1.1.49)
To measure glucose-6-phosphate dehydrogenase activity, beta-nicotinamide adenine dinucleotide phosphate is used in a spectrophotometric rate determination assay at 340 nm.
Analysis of PFAS in Food Packaging
PFAS analysis in food contact materials for 25 compounds using Supelclean™ ENVI-WAX™ SPE and Ascentis® Express PFAS columns by LC-MS/MS.
6-磷酸葡萄糖脱氢酶（EC 1.1.1.49）的酶学测定
在测定6-磷酸葡萄糖脱氢酶活性时，使用β-烟酰胺腺嘌呤二核苷酸磷酸在340 nm处通过分光光度法进行测定。
Pharmaceutical Secondary Standards
Convenient and cost-effective alternative to primary reference standards, with traceability to USP, BP, EP standards; manufactured to ISO/IEC 17025 and ISO Guide 34.
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