rabbit polyclonal 3025s Search Results


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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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Millipore phdac5 s259
(A) Western blotting of <t>PGES2</t> protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.
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Image Search Results


(A) Western blotting of PGES2 protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.

Journal: PLoS Biology

Article Title: Ablating astrocyte insulin receptors leads to delayed puberty and hypogonadism in mice

doi: 10.1371/journal.pbio.3000189

Figure Lengend Snippet: (A) Western blotting of PGES2 protein expression from FACS-isolated astrocytes were imaged and quantified for IR loxp and IRKO GFAP mice. IR loxp (black bar) and IRKO GFAP (white bar), ( n = 4 per group, 2 brains pooled per lane). Values are expressed as means ± SEM. * P < 0.05 IRKO GFAP versus IR loxp group. The underlying data can be found in . (B–C) Schematic diagram representing the mechanism of astrocyte modulation of HPG axis. FACS, fluorescence-activated cell sorting; HPG, hypothalamic pituitary gonadotropin; IR, insulin receptor; IRKO GFAP , astrocyte-specific insulin receptor deletion; PGES2, prostaglandin E synthase 2.

Article Snippet: The primary antibodies used were as follows: IRβ (Cat. #3025S, Cell signaling); PGES2 (Cat. #bs-2639R, Bioss) [ , ]; and GADPH (Cat.# SC-32233, Santa Cruz Biotechnology).

Techniques: Western Blot, Expressing, Isolation, Fluorescence, FACS