Binding affinity of Lili-Mip1, 2 and 3 with different fatty acids.
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Intrinsic Tryptophan fluorescence intensity change is employed to measure the binding affinities of Lili-Mip1, 2 and 3 for different fatty acids. All values are in μM. The protein is in 50mM sodium acetate buffer pH 4.8, 100mM NaCl. The experiments are repeated with three biological replicates, n = 3 and are drawn as mean ± S.D.
创建时间：
2023-06-29
