Retinol Binding Protein RBP Antibody

Western Blot: Retinol Binding Protein RBP Antibody [NBP2-20132] - Elevation of retinal tissue induction of visual cycle enzymes stimulated by retinoic acid 6 (STRA6, C) in chrysin-treated mice. The db/db mice were orally supplemented with 10 mg/kg of chrysin daily for 10 weeks. The db/m mice were introduced as control animals. Mouse retinal tissue extracts were subject to Western blot analysis with a primary antibody against each target protein of LRAT, RDH5, cellular retinol binding protein (CRBP), CRALBP, IRBP, or STRA6. beta-actin protein was used as an internal control. Bar graphs (mean +- SEM, n = nine independent experiments) in the bottom or right panels represent densitometric results of upper blot bands. * Values in bar graphs indicate a significant difference at p<0.05.

Western Blot: Retinol Binding Protein RBP Antibody [NBP2-20132] - Elevation of retinal tissue induction of visual cycle enzymes stimulated by retinoic acid 6 (STRA6, C) in chrysin-treated mice. The db/db mice were orally supplemented with 10 mg/kg of chrysin daily for 10 weeks. The db/m mice were introduced as control animals. Mouse retinal tissue extracts were subject to Western blot analysis with a primary antibody against each target protein of LRAT, RDH5, cellular retinol binding protein (CRBP), CRALBP, IRBP, or STRA6. beta-actin protein was used as an internal control. Bar graphs (mean +- SEM, n = nine independent experiments) in the bottom or right panels represent densitometric results of upper blot bands. * Values in bar graphs indicate a significant difference at p<0.05.

Western Blot: Retinol Binding Protein RBP Antibody [NBP2-20132] - Elevation of retinal tissue induction of visual cycle enzymes stimulated by retinoic acid 6 (STRA6, C) in chrysin-treated mice. The db/db mice were orally supplemented with 10 mg/kg of chrysin daily for 10 weeks. The db/m mice were introduced as control animals. Mouse retinal tissue extracts were subject to Western blot analysis with a primary antibody against each target protein of LRAT, RDH5, cellular retinol binding protein (CRBP), CRALBP, IRBP, or STRA6. beta-actin protein was used as an internal control. Bar graphs (mean +- SEM, n = nine independent experiments) in the bottom or right panels represent densitometric results of upper blot bands. * Values in bar graphs indicate a significant difference at p<0.05.