<p>The EcR panel represents EcR levels in accessory glands from EcR control (+ lane, EcR), EcR knockdown (-lane, EcR), USP control (+ lane, USP) and USP knockdown (- lane, USP). Similarly, the USP panel represents the USP levels observed in accessory glands from above groups. Blots probed with α-tubulin antibodies (α-tubulin panels) served as controls for protein loading. Knockdowns were specific to the targeted hormone receptor. Further, the deficiency of EcR did not affect USP levels and vice-versa.</p
The same samples in Fig 2 were used to examine collagen 1, collagen 3, and fibronectin as ECM protei...
<p>A. Representative western blots of target proteins and β-actin, the standard. At least two gels w...
<p>(A) Representative western blot showing the levels of the proteins Nanog, Klf4 and c-Myc in MDA-M...
<p>Immunofluorescence panels shown here are the overlay images of accessory glands immunostained wit...
<p>To assess the effect of depletion of EcR or USP, accessory glands were analyzed either at the ult...
<p>Protein extracts were prepared from salivary glands of three different crosses at the wandering-L...
<p>Protein extracts were prepared from salivary glands of seven different crosses at the wandering-L...
<p>(A) The MCF7 cells were cultured under hormone starvation conditions for 3–4 days and then treate...
<p>H1R protein expression levels were quantified for males (n = 5), OVX females (oil injected contro...
<p>Actin was used as a control for loading protein. <b>B</b>) Histograms representing the quantifica...
<p>(A) EcR and USP genes were quickly up-regulated when entering the wandering stage. The transcript...
<p>Immunoblots for total and/or phosphorylated AKT, 4E-BP1, 4E-BP2, and S6K1 are presented for both ...
<p><b>A.</b> Western blot analysis was used to detect the protein level of ET<sub>B</sub> receptor i...
<p><b>Copyright information:</b></p><p>Taken from "Cytochrome P450arom, androgen and estrogen recept...
<p>(Panel A) Western blot analysis of ERα S118 phosphorylation in MCF-7 cells treated with vehicle (...
The same samples in Fig 2 were used to examine collagen 1, collagen 3, and fibronectin as ECM protei...
<p>A. Representative western blots of target proteins and β-actin, the standard. At least two gels w...
<p>(A) Representative western blot showing the levels of the proteins Nanog, Klf4 and c-Myc in MDA-M...
<p>Immunofluorescence panels shown here are the overlay images of accessory glands immunostained wit...
<p>To assess the effect of depletion of EcR or USP, accessory glands were analyzed either at the ult...
<p>Protein extracts were prepared from salivary glands of three different crosses at the wandering-L...
<p>Protein extracts were prepared from salivary glands of seven different crosses at the wandering-L...
<p>(A) The MCF7 cells were cultured under hormone starvation conditions for 3–4 days and then treate...
<p>H1R protein expression levels were quantified for males (n = 5), OVX females (oil injected contro...
<p>Actin was used as a control for loading protein. <b>B</b>) Histograms representing the quantifica...
<p>(A) EcR and USP genes were quickly up-regulated when entering the wandering stage. The transcript...
<p>Immunoblots for total and/or phosphorylated AKT, 4E-BP1, 4E-BP2, and S6K1 are presented for both ...
<p><b>A.</b> Western blot analysis was used to detect the protein level of ET<sub>B</sub> receptor i...
<p><b>Copyright information:</b></p><p>Taken from "Cytochrome P450arom, androgen and estrogen recept...
<p>(Panel A) Western blot analysis of ERα S118 phosphorylation in MCF-7 cells treated with vehicle (...
The same samples in Fig 2 were used to examine collagen 1, collagen 3, and fibronectin as ECM protei...
<p>A. Representative western blots of target proteins and β-actin, the standard. At least two gels w...
<p>(A) Representative western blot showing the levels of the proteins Nanog, Klf4 and c-Myc in MDA-M...