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oas1  (Proteintech)


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    Proteintech oas1
    Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of <t>OAS1</t> mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group
    Oas1, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 42 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/14955+1+ap/OAS1+Antibody/pmc12745338-271-12-38
    Average 93 stars, based on 42 article reviews
    oas1 - by Bioz Stars, 2026-09
    93/100 stars

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    1) Product Images from "Activated oligoadenylate synthetase-ribonuclease L pathway promotes endothelial pyroptosis and impairs diabetic wound healing via thioredoxin-interacting protein m 6 A methylation"

    Article Title: Activated oligoadenylate synthetase-ribonuclease L pathway promotes endothelial pyroptosis and impairs diabetic wound healing via thioredoxin-interacting protein m 6 A methylation

    Journal: Molecular Biomedicine

    doi: 10.1186/s43556-025-00399-9

    Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of OAS1 mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group
    Figure Legend Snippet: Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of OAS1 mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group

    Techniques Used: Expressing, Immunofluorescence, Dot Blot, Quantitative RT-PCR, Western Blot

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    Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of <t>OAS1</t> mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group
    Oas1, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    oas1 14 955 1 ap antibody  (Proteintech)
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    Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of <t>OAS1</t> mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group
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    Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of <t>OAS1</t> mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group
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    Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of <t>OAS1</t> mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group
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    Image Search Results


    Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of OAS1 mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group

    Journal: Molecular Biomedicine

    Article Title: Activated oligoadenylate synthetase-ribonuclease L pathway promotes endothelial pyroptosis and impairs diabetic wound healing via thioredoxin-interacting protein m 6 A methylation

    doi: 10.1186/s43556-025-00399-9

    Figure Lengend Snippet: Elevated expression of OSA-RNase L in the HUVECs stimulated by high glucose. Immunofluorescence assay and semi-quantitative analysis of dsRNA ( a - b ). dot blot assay of dsRNA in the diabetic mouse skin ( c ). RT-qPCR assay of OAS1 mRNA ( d ), OAS2 mRNA ( e ), OAS3 mRNA ( f ), RNase L mRNA ( g ) expression in HUVECs stimulated by high glucose. Western blot assay of OAS1, OAS2, OAS3 and RNase L protein ( h ), and immunofluorescence assay and semi-quantitative analysis of OAS1, OAS2, OAS3 and RNase L (i-p). The results are presented as the mean ± SEM, * p < 0.05, ** p < 0.01, **** p < 0.0001. Each experiment was replicated for thrice. The number of mice used in this experiment was four per group

    Article Snippet: The membranes were incubated overnight at 4 °C with specific primary antibodies: OAS1 (14955-1-AP), OAS2 (19279-1-AP), OAS3 (21915-1-AP), RNase L (22577-1-AP), NLRP3 (19771-1-AP), GSDMD (20770-1-AP), IL-1β (16806-1-AP), IL-18 (10663-1-AP), METTL3 (15073-1-AP), TXNIP (18243-1-AP), and Tubulin (10094-1-AP), all from Proteintech (Wuhan, China).

    Techniques: Expressing, Immunofluorescence, Dot Blot, Quantitative RT-PCR, Western Blot