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Mixing was carried out with wheat flour alone or supplemented with different ingredients (alone or in combination) such as Y, G and HB (1%) or SB (0.5%) flour.
Representative John M. Zerwas, Republican of Simonton and the chairman of a budget subcommittee on health and human services, said HB 1 should be viewed as a proposal, not as a finished document.
On Romney: "The one percent!" And Gingrich: "The lobbyist for the one percent!" On his first legislative priorities as president: "HB 1 campaign reform, HB 2 fair trade, HB 3 energy independence, HB 4 tax reform!" On his cabinet: "It'd be white and black, man and woman.
Transferase activity is given as U/gm Hb (1 unit = 1 μmol UDPG /hr).
With increasing concentrations of total NF-κB (Fig. 2A, from right to left), the dynamics of active NF-κB change from a monotone increase and damped oscillations to sustained oscillations at the Hopf bifurcation point (Fig. 2A, HB 1).
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The primary endpoint was Hb response (defined as Hb reaching ≥10 g/dL, an increase of Hb ≥1 g/dL since inclusion visit or reaching physician-defined target Hb, with no blood transfusions in the 3 weeks prior to measurement).
Copolymers containing (R -3-hydroxybutyric acid (HB), 1,4-butanediol (B), and adipic acid (A) weR -3-hydroxybutyricicR -3-hydroxybutyricnsesterificacidn of biodegradable poly(R-3-HBdroxybutyrate) (PHB) and poly(1,4-butanediolipate) (PBandin solution adipicferent reacidon times, composition of the stArting mixture, and amount of 4-toluenesulfonic acid, used as a catalyst.
Unstable hemoglobin (Hb) variants, such as HbC, sickle HbS, and unpaired beta globin chains present in α-thalassemic states, impart a greatly increased level of oxidative stress on erythrocytes that enhances the oxidative denaturation of Hb [1] [5].
Finally the nuclei pellet was resuspended in 1 mL of filtered HB 1× and embedded in 1.2% low-melting-point agarose plugs (InCert Agarose, Cambrex-Bioscience, Rockland, Inc).
Fifty grams of young leaves were ground in liquid nitrogen and nuclei were liberated by incubating the cell extract at 4°C for 20 min in HB 1× extraction buffer, plus 0.2% of polyvinylpyrrolidone (PVP 40).
The nuclei was washed in 20 mL of HB 1× extraction buffer without β-mercaptoethanol and Triton-100×, and then centrifuged at 850 × g for 8 min at 4°C.
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