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phosphoret tyr 905  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc phosphoret tyr 905
    Phosphoret Tyr 905, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+ret/Ret+Rabbit+mAb/pm41792117-354-34-37
    Average 94 stars, based on 17 article reviews
    phosphoret tyr 905 - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    other:

    Article Title: FAT4 fine-tunes kidney development by regulating RET signaling
    Article Snippet: Rabbit anti-RET , Cell Signaling , #3223.

    Incubation:

    Article Title: Hedgehog-dependent and Hedgehog-independent roles for Growth Arrest Specific 1 in mammalian kidney morphogenesis
    Article Snippet: Duolink® Proximity Ligation Assay (PLA; Sigma; DUO92007) was performed according to the manufacturer’s instructions. .. Sections were blocked (1X PBS+ 10% Donkey serum + 0.3% Triton) for 1 h at 37°C, then incubated with rabbit anti-RET (1:200, Cell Signaling, Cat3223) and goat anti-GAS1 (1:900, R&D Systems; Cat#AF2544) or goat anti- GFRA1 (1:500, R&D Systems, Cat# AF560) overnight at 4°C. .. The next day, slides were incubated with PLA Probe Anti-Rabbit PLUS (Sigma; DUO92002) and PLA Probe Anti-Goat Minus (Sigma; DUO92006).



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    Pz-1-based PROTACs activity on CCDC6-RET. TPC1 cells were treated with the indicated PROTACs or Pz-1 for 12 h at the indicated concentrations. Cells were harvested, and extracts were subjected to Western blotting with anti-RET antibody. Tubulin was used as a loading control.

    Journal: Scientific Reports

    Article Title: Discovery of a Proteolysis Targeting Chimera for TRKA and RET-derived oncoproteins

    doi: 10.1038/s41598-025-25687-w

    Figure Lengend Snippet: Pz-1-based PROTACs activity on CCDC6-RET. TPC1 cells were treated with the indicated PROTACs or Pz-1 for 12 h at the indicated concentrations. Cells were harvested, and extracts were subjected to Western blotting with anti-RET antibody. Tubulin was used as a loading control.

    Article Snippet: Antibodies for VEGFR2 (2479), phospho-TRKA (Tyr490) (9141), phospho-TRKA (Tyr674/675) (4621), panTRK (A7H6R) (92991) and RET (14698) were from Cell Signaling Technology (Beverly, MA, USA).

    Techniques: Activity Assay, Western Blot, Control

    Compound 9 activity on RET- and TRKA-driven cell proliferation. The indicated cell lines were incubated with vehicle (NT: not treated) or increasing concentrations of compound 9 and counted at the indicated time points. Data are the mean ± SD of a single experiment performed in triplicate. Number of cells plated at Day 0: KM12 (10,000/well); TT (200,000/well); TPC-1 (5000/well); MZ-CRC-1 and Lc-2/ad (100,000/well). IC 50 dose was calculated using PRIZM software (GraphPad Software Inc). Confidence intervals are indicated in brackets.

    Journal: Scientific Reports

    Article Title: Discovery of a Proteolysis Targeting Chimera for TRKA and RET-derived oncoproteins

    doi: 10.1038/s41598-025-25687-w

    Figure Lengend Snippet: Compound 9 activity on RET- and TRKA-driven cell proliferation. The indicated cell lines were incubated with vehicle (NT: not treated) or increasing concentrations of compound 9 and counted at the indicated time points. Data are the mean ± SD of a single experiment performed in triplicate. Number of cells plated at Day 0: KM12 (10,000/well); TT (200,000/well); TPC-1 (5000/well); MZ-CRC-1 and Lc-2/ad (100,000/well). IC 50 dose was calculated using PRIZM software (GraphPad Software Inc). Confidence intervals are indicated in brackets.

    Article Snippet: Antibodies for VEGFR2 (2479), phospho-TRKA (Tyr490) (9141), phospho-TRKA (Tyr674/675) (4621), panTRK (A7H6R) (92991) and RET (14698) were from Cell Signaling Technology (Beverly, MA, USA).

    Techniques: Activity Assay, Incubation, Software