Figure 7From: OpenFLUX2: 13C-MFA modeling software package adjusted for the comprehensive analysis of single and parallel labeling experiments The values of the normalized flux precision function in the different parts of the assumed metabolic network depend significantly on the applied tracer(s). The results of flux estimation: (A) SLE using 100% [1-13C]-glucose as the tracer; and from PLEs consisting of: (B) 5 LEs using different mixtures of [U-13C]/[U-12C]-glucose in each LE, with 20%, 35%, 50%, 65%, or 80% [U-13C]-glucose; (C) 5 LEs using partially optimized mixtures of [1-13C]/[U-12C]/[U-13C] glucose for the separate minimization of the approximated variances of the θ 10, θ 12, θ 14, θ 22, θ 31 free fluxes in each LE; (D) 3 LEs using 100% [1-13C]-, [3-13C]-, or [4-13C]-glucose as a tracer; (E) 6 LEs, where 3 of the LEs used in (D) corresponded to partial optimization for θ 4andθ 12, θ 14, θ 22andθ 31, respectively, and 3 other LEs used the partially optimized mixture of [1-13C]/[3-13C]/[4-13C]-glucose to minimize the approximated variances of the θ 8, θ 10, θ 26 free fluxes. The values of the normalized flux precision function for all fluxes are indicated by the color-scored grade.Back to article page