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GE Healthcare
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Cytiva Europe
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AMRAD Corporation
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Biotech AB
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Image Search Results
Journal:
Article Title: Engineering a nicking endonuclease N. Alw I by domain swapping
doi: 10.1073/pnas.241215698
Figure Lengend Snippet: Measurement of the molecular mass of AlwI and N.AlwI by gel filtration. (A) HiPrep 26/60 Sephacryl-100 (with a total bed volume Vt = 318 ml) was used to determine the molecular mass of N.AlwI under native conditions. The elution volume of blue Dextran 2000 (2,000 kDa) was used to determine the void volume (Vo). The elution volumes (Ve) of protein standards BSA (67 kDa), ovalbumin (43 kDa), chymotrypsinogen A (25 kDa), and ribonuclease A (13.7 kDa) were measured. The partition coefficient (Kav) is calculated as (Ve − Vo)/(Vt − Vo). The standard curve was obtained by plotting Kav against the log of the molecular mass (logMr). The Kav of N.AlwI was obtained (0.11), and its molecular weight was determined by using the standard curve. (B) HiPrep 26/60 Sephacryl-300 was used to determine the molecular weight of AlwI following the same procedure as N.AlwI. Protein standards used were catalase (232 kDa), aldolase (158 kDa), BSA (67 kDa), and ovalbumin (43 kDa). The Kav of AlwI was 0.28.
Article Snippet:
Techniques: Filtration, Molecular Weight