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文献和实验Fluorescence-Based Technique for Analyzing Retinoic Acid
retinoic acid-binding protein I (CRABP-I), a protein that binds RA with high affinity and specificity, as a “read-out” for its ligand. Replacing 28 Leu of CRABP-I with a Cys residue allows for covalently attaching an environmentally sensitive
Antisense methodologies have been used extensively to inhibit the expression of specific genes with a view to elucidating their role in particular cellular processes ( 1 ). The technique is based on the ability of mRNA to bind
Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR) for Cellular Retinoid-Binding Proteins
Cellular retinoid-binding proteins were first identified in the mid-1970s (1 ). Subsequent studies established the existence of two forms of cellular retinoic acid-binding proteins (CRABPI and II) (2 , 3 ) and two forms of cellular retinol
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