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Reaction buffers for use in experiments involving modifying enzymes. Different buffer solutions create optimal reaction conditions for specific modifying enzymes, or facilitate multiple enzymatic reactions.
Thermo Scientific enzymes for in vitro transcription are designed for efficient and reliable RNA synthesis. These enzymes cover the entire synthesis workflow from template preparation to post-transcriptional modifications, ensuring optimal performance and high yields of synthesized RNA.
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GSA/VA Contract Available on GSA/VA contract for Federal Government customers. Learn More
Specifically digests the agarose polysaccharide core, which allows for gentle yet efficient recovery of DNA or RNA fragments from low melting point agarose.
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Pyruvate Kinase (PK) is a glycolysis enzyme and has four isozymes L R M1 and M2. The L isozyme is localized in gluconeogenic tissues particularly in the liver. Whereas the R and M1 are localized in the adult skeletal muscles heart brain and erythrocytes respectively. M2 is localized in the nucleus of the cells.
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Proteinase K (PK) from fungi Tritirachium album encodes a 40 kDa protein. The N-terminal propeptide region shows homology with bacterial subtilisin. PK crystallizes even under microgravity conditions on the space shuttle mission. PK is an effective protein system for studying protein engineering process.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Pyruvate Kinase, Microorganism (PK) is a glycolytic enzyme that catalyzes the conversion of phosphoenolpyruvate and ADP to pyruvate and ATP. This product is for research use only.
Catalyzes conversion of phosphoenolpyruvate and ADP to pyruvate and ATP
Theoretical molecular weight: 237 kDa
Optimum pH: 7.0-7.5
Appears as a white to off-white solid
For research use only
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More