DescriptionPCP4 Western blot with knock-down and control H295R adrenocortical cells.jpg
English: Western blotting of PCP4 (down, 7.6kDa) and beta-actin (control marker, up, 42kDa) in two samples of H295R human adrenocortical carcinoma cells. Sample number 1 was submitted to PCP4 transient knockdown using a MISSION® esiRNA (SIGMA-ALDRICH), while sample number 2 was transfected with a universal negative-control siRNA. H295R cells were transfected using a Nucleofector-4D (LONZA). All methods were carried out as published by Felizola SJA et al 2014 Journal of Molecular Endocrinology 52(2):159-67. doi: 10.1530/JME-13-0248.[1]
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Western blotting of PCP4 and beta-actin (control marker) in two samples of H295R human adrenal cortex carcinoma cell line according to published methods.
English: Western blotting of PCP4 (down, 7.6kDa) and beta-actin (control marker, up, 42kDa) in two samples of H295R human adrenal carcinoma cells. Sample number 1 was submitted to PCP4 transient knockdown using a MISSION® esiRNA (SIGMA-ALDRICH), while sample number 2 was transfected with a universal negative-control siRNA. H295R cells were transfected using a Nucleofector-4D (LONZA). PCP4 antibody (rabbit anti-human, polyclonal) was purchased from SIGMA-ALDRICH and used at 1:400 concentration. All methods were carried out as published by Felizola SJA et al 2014 Journal of Molecular Endocrinology 52(2):159-67. doi: 10.1530/JME-13-0248.[1]
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