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anti phospho m csf receptor tyr723 rabbit mab  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti phospho m csf receptor tyr723 rabbit mab
    Anti Phospho M Csf Receptor Tyr723 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 47 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/m+csf+receptor/Phospho-CSF-1R%2FM-CSF-R+(Tyr723)+Rabbit+mAb/pmc12765947-29-0-8
    Average 93 stars, based on 47 article reviews
    anti phospho m csf receptor tyr723 rabbit mab - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    FACS:

    Article Title: The RUNX1/IL-34/CSF-1R axis is an autocrinally regulated modulator of resistance to BRAF-V600E inhibition in melanoma
    Article Snippet: Primary antibodies were followed by incubation with horseradish peroxidase-conjugated anti-mouse (Santa Cruz Biotechnologies Inc., catalog sc-358914) or anti-rabbit secondary antibodies (Cell Signalling Technologies, catalog7074), and the blots were developed with the Western Lightning Plus-ECL system (Perkin-Elmer). .. For FACS-analysis, the M-CSF Receptor (PE Conjugate) antibody (Cell Signalling Technologies, 65396) was used. ..

    Article Title: The RUNX1/IL-34/CSF-1R axis is an autocrinally regulated modulator of resistance to BRAF-V600E inhibition in melanoma.
    Article Snippet: Primary antibodies were followed by incubation with horseradish peroxidase-conjugated anti-mouse (Santa Cruz Biotechnologies Inc., catalog sc-358914) or anti-rabbit secondary antibodies (Cell Signalling Technologies, catalog7074), and the blots were developed with the Western Lightning Plus-ECL system (Perkin-Elmer). .. For FACS-analysis, the M-CSF Receptor (PE Conjugate) antibody (Cell Signalling Technologies, 65396) was used. ..

    other:

    Article Title: STING regulates peripheral nerve regeneration and colony stimulating factor 1 receptor (CSF1R) processing in microglia
    Article Snippet: M-CSF Receptor, Rabbit, pAbs , Cell Signaling Technology , Cat# 3152, RRID: AB_2085233.

    Article Title: THE MAPK ERK5, BUT NOT ERK1/2, INHIBITS THE PROGRESSION OF MONOCYTIC PHENOTYPE TO THE FUNCTIONING MACROPHAGE
    Article Snippet: Phospho-Erk1/2 (Thr202/Tyr204, #9101), Erk1/2 (#9102), phospho-ERK5 (Thr187/Tyr220, #3371), Erk5 (#3372), M-CSF Receptor (#3152), anti-rabbit (#7074) and anti-mouse (#7076) antibodies linked to HRP were purchased from Cell Signaling Technologies.



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    Image Search Results


    Aldosterone activates the MR/M-CSF/M-CSFR pathway. ( A ) The expression of NR3C2 in VSMC nuclei. Scale bar = 50 μm. n = 3. ( B ) Immunofluorescence analysis of M-CSF in the aortas of aldosterone-infused rats. Scale bars = 100 μm. n = 3. ( C ) The co-expression of F4/80 and p-MCSFR were detected by immunofluorescence staining; F4/80 is shown in green, p-MCSFR is shown in red, and DAPI is shown in blue. Scale bars = 20 μm. n = 3. ( D ) Western blot analysis of the expression of NR3C2 (total and nuclear), SGK1, M-CSF, p-MCSFR, and M-CSFR in VSMCs. n = 6. ( E ) The concentration of M-CSF in the VSMCs culture medium was detected via ELISA. n = 6. ( F ) Flow cytometry analysis of VSMCs after different treatments (ALD, ESA, M-CSF, M-CSF+PLX3397, ALD+PLX3397, and M-CSF+ESA). # p < 0.05 compared with CON; * p < 0.05 compared with ALD. ALD: aldosterone stimulation; ESA: esaxerenone treatment; SGK1: serum- and glucocorticoid-inducible kinase 1; NR3C2: nuclear receptor subfamily 3, group C, member 2; and MR: mineralocorticoid receptor.

    Journal: International Journal of Molecular Sciences

    Article Title: Aldosterone-Induced Transformation of Vascular Smooth Muscle Cells into Macrophage-like Cells Participates in Inflammatory Vascular Lesions

    doi: 10.3390/ijms26073345

    Figure Lengend Snippet: Aldosterone activates the MR/M-CSF/M-CSFR pathway. ( A ) The expression of NR3C2 in VSMC nuclei. Scale bar = 50 μm. n = 3. ( B ) Immunofluorescence analysis of M-CSF in the aortas of aldosterone-infused rats. Scale bars = 100 μm. n = 3. ( C ) The co-expression of F4/80 and p-MCSFR were detected by immunofluorescence staining; F4/80 is shown in green, p-MCSFR is shown in red, and DAPI is shown in blue. Scale bars = 20 μm. n = 3. ( D ) Western blot analysis of the expression of NR3C2 (total and nuclear), SGK1, M-CSF, p-MCSFR, and M-CSFR in VSMCs. n = 6. ( E ) The concentration of M-CSF in the VSMCs culture medium was detected via ELISA. n = 6. ( F ) Flow cytometry analysis of VSMCs after different treatments (ALD, ESA, M-CSF, M-CSF+PLX3397, ALD+PLX3397, and M-CSF+ESA). # p < 0.05 compared with CON; * p < 0.05 compared with ALD. ALD: aldosterone stimulation; ESA: esaxerenone treatment; SGK1: serum- and glucocorticoid-inducible kinase 1; NR3C2: nuclear receptor subfamily 3, group C, member 2; and MR: mineralocorticoid receptor.

    Article Snippet: The VSMCs were treated with M-CSF (MCE, Shanghai, China, cat. no. Hy-p7085) at a dose of 10 −7 mol/L in the subsequent experiments with or without the M-CSF receptor inhibitor PLX3397 (MCE, Shanghai, China, cat. no. Hy-16749) at a dose of 10 −7 mol/L.

    Techniques: Expressing, Immunofluorescence, Staining, Western Blot, Concentration Assay, Enzyme-linked Immunosorbent Assay, Flow Cytometry