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rabbit anti rad18 polyclonal antibody  (Proteintech)


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    Structured Review

    Proteintech rabbit anti rad18 polyclonal antibody
    <t>RAD18</t> expression in CSCC with different genetic polymorphisms as determined by immunohistochemistry (40× objective, magnified). (A) rs250403-AA; (B) rs250403-AG; (C) rs250403-GG; (D) rs615967-AA; (E) rs615967-AG; (F) rs615967-GG. The distinct brown coloration is mainly located in the nucleus of the positive cells.
    Rabbit Anti Rad18 Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti rad18 polyclonal antibody/product/Proteintech
    Average 93 stars, based on 20 article reviews
    rabbit anti rad18 polyclonal antibody - by Bioz Stars, 2026-03
    93/100 stars

    Images

    1) Product Images from "Risk of cervical squamous cell carcinoma associated with a single nucleotide polymorphism in the RAD18 gene in the Chinese population and its significance as a predictive biomarker"

    Article Title: Risk of cervical squamous cell carcinoma associated with a single nucleotide polymorphism in the RAD18 gene in the Chinese population and its significance as a predictive biomarker

    Journal: Medicine

    doi: 10.1097/MD.0000000000044017

    RAD18 expression in CSCC with different genetic polymorphisms as determined by immunohistochemistry (40× objective, magnified). (A) rs250403-AA; (B) rs250403-AG; (C) rs250403-GG; (D) rs615967-AA; (E) rs615967-AG; (F) rs615967-GG. The distinct brown coloration is mainly located in the nucleus of the positive cells.
    Figure Legend Snippet: RAD18 expression in CSCC with different genetic polymorphisms as determined by immunohistochemistry (40× objective, magnified). (A) rs250403-AA; (B) rs250403-AG; (C) rs250403-GG; (D) rs615967-AA; (E) rs615967-AG; (F) rs615967-GG. The distinct brown coloration is mainly located in the nucleus of the positive cells.

    Techniques Used: Expressing, Immunohistochemistry



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    <t>RAD18</t> expression in CSCC with different genetic polymorphisms as determined by immunohistochemistry (40× objective, magnified). (A) rs250403-AA; (B) rs250403-AG; (C) rs250403-GG; (D) rs615967-AA; (E) rs615967-AG; (F) rs615967-GG. The distinct brown coloration is mainly located in the nucleus of the positive cells.
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    RFWD3 ubiquitin ligase activity regulates PCNA ubiquitylation in human cells (A) U2OS cells or U2OS cells expressing Strep-HA-PCNA were transfected with siCtrl or 4 different siRNAs against RFWD3 and either left untreated or treated with UV (30 J/m 2 ). PCNA was recovered under denaturing conditions via Strep-Tactin pull-down and analyzed by immunoblotting with the indicated antibodies. (B) U2OS cells or U2OS/FRT GFP-RFWD3 WT or catalytic inactive (C315A) cells were treated with the indicated siRNAs, transfected with either empty vector (EV) or Strep-HA-PCNA plasmids, and treated with doxycycline to induce expression of RFWD3. UV treatment and protein pull-down were performed as in (A). (C) U2OS cells were transfected with the indicated plasmids and then subjected to Strep-Tactin pull-down as in (A). (D) U2OS/FRT GFP-RFWD3 WT cells were treated with doxycycline and transfected with EV or Strep-HA-PCNA 24 h before lysis in denaturing buffer. Lysates were subjected to Strep-Tactin pull-down in denaturing conditions, washed, and incubated with USP2 (ubiquitin protease) and/or UPL1 (SUMO protease), as indicated. (E) U2OS cells or U2OS/FRT GFP-RFWD3 WT cells were transfected with either control (siCtrl) or <t>RAD18</t> siRNAs. After 48 h, cells were transfected with either EV or Strep-HA-PCNA plasmids and treated with doxycycline to induce the expression RFWD3 WT. Then, cells were treated with UV for 4 h and processed for Strep-Tactin pull-down as described in (A). The asterisk denotes a non-specific band.
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    RFWD3 ubiquitin ligase activity regulates PCNA ubiquitylation in human cells (A) U2OS cells or U2OS cells expressing Strep-HA-PCNA were transfected with siCtrl or 4 different siRNAs against RFWD3 and either left untreated or treated with UV (30 J/m 2 ). PCNA was recovered under denaturing conditions via Strep-Tactin pull-down and analyzed by immunoblotting with the indicated antibodies. (B) U2OS cells or U2OS/FRT GFP-RFWD3 WT or catalytic inactive (C315A) cells were treated with the indicated siRNAs, transfected with either empty vector (EV) or Strep-HA-PCNA plasmids, and treated with doxycycline to induce expression of RFWD3. UV treatment and protein pull-down were performed as in (A). (C) U2OS cells were transfected with the indicated plasmids and then subjected to Strep-Tactin pull-down as in (A). (D) U2OS/FRT GFP-RFWD3 WT cells were treated with doxycycline and transfected with EV or Strep-HA-PCNA 24 h before lysis in denaturing buffer. Lysates were subjected to Strep-Tactin pull-down in denaturing conditions, washed, and incubated with USP2 (ubiquitin protease) and/or UPL1 (SUMO protease), as indicated. (E) U2OS cells or U2OS/FRT GFP-RFWD3 WT cells were transfected with either control (siCtrl) or <t>RAD18</t> siRNAs. After 48 h, cells were transfected with either EV or Strep-HA-PCNA plasmids and treated with doxycycline to induce the expression RFWD3 WT. Then, cells were treated with UV for 4 h and processed for Strep-Tactin pull-down as described in (A). The asterisk denotes a non-specific band.
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    Image Search Results


    RAD18 expression in CSCC with different genetic polymorphisms as determined by immunohistochemistry (40× objective, magnified). (A) rs250403-AA; (B) rs250403-AG; (C) rs250403-GG; (D) rs615967-AA; (E) rs615967-AG; (F) rs615967-GG. The distinct brown coloration is mainly located in the nucleus of the positive cells.

    Journal: Medicine

    Article Title: Risk of cervical squamous cell carcinoma associated with a single nucleotide polymorphism in the RAD18 gene in the Chinese population and its significance as a predictive biomarker

    doi: 10.1097/MD.0000000000044017

    Figure Lengend Snippet: RAD18 expression in CSCC with different genetic polymorphisms as determined by immunohistochemistry (40× objective, magnified). (A) rs250403-AA; (B) rs250403-AG; (C) rs250403-GG; (D) rs615967-AA; (E) rs615967-AG; (F) rs615967-GG. The distinct brown coloration is mainly located in the nucleus of the positive cells.

    Article Snippet: The sections were firstly incubated with Rabbit anti-RAD18 Polyclonal antibody (1:200, 18333-1-AP, Proteintech), and then incubated with Dako Envision TM Peroxidase (Dako Diagnostica, Hamburg, Germany), and visualized with 3,3’-diaminobenzidine tetrahydrochloride (Dako).

    Techniques: Expressing, Immunohistochemistry

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: Fanconi anemia-associated chromosomal radial formation is dependent on POLθ-mediated alternative end joining

    doi: 10.1016/j.celrep.2023.112428

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit polyclonal anti-RAD18 , Bethyl Laboratories , Cat # A301–340A; RRID: AB_937974.

    Techniques: Recombinant, Membrane, Plasmid Preparation, Staining, Transfection, Reverse Transcription, Software, Real-time Polymerase Chain Reaction, Microscopy, Cell Counting

    RFWD3 ubiquitin ligase activity regulates PCNA ubiquitylation in human cells (A) U2OS cells or U2OS cells expressing Strep-HA-PCNA were transfected with siCtrl or 4 different siRNAs against RFWD3 and either left untreated or treated with UV (30 J/m 2 ). PCNA was recovered under denaturing conditions via Strep-Tactin pull-down and analyzed by immunoblotting with the indicated antibodies. (B) U2OS cells or U2OS/FRT GFP-RFWD3 WT or catalytic inactive (C315A) cells were treated with the indicated siRNAs, transfected with either empty vector (EV) or Strep-HA-PCNA plasmids, and treated with doxycycline to induce expression of RFWD3. UV treatment and protein pull-down were performed as in (A). (C) U2OS cells were transfected with the indicated plasmids and then subjected to Strep-Tactin pull-down as in (A). (D) U2OS/FRT GFP-RFWD3 WT cells were treated with doxycycline and transfected with EV or Strep-HA-PCNA 24 h before lysis in denaturing buffer. Lysates were subjected to Strep-Tactin pull-down in denaturing conditions, washed, and incubated with USP2 (ubiquitin protease) and/or UPL1 (SUMO protease), as indicated. (E) U2OS cells or U2OS/FRT GFP-RFWD3 WT cells were transfected with either control (siCtrl) or RAD18 siRNAs. After 48 h, cells were transfected with either EV or Strep-HA-PCNA plasmids and treated with doxycycline to induce the expression RFWD3 WT. Then, cells were treated with UV for 4 h and processed for Strep-Tactin pull-down as described in (A). The asterisk denotes a non-specific band.

    Journal: Molecular Cell

    Article Title: The ubiquitin ligase RFWD3 is required for translesion DNA synthesis

    doi: 10.1016/j.molcel.2020.11.029

    Figure Lengend Snippet: RFWD3 ubiquitin ligase activity regulates PCNA ubiquitylation in human cells (A) U2OS cells or U2OS cells expressing Strep-HA-PCNA were transfected with siCtrl or 4 different siRNAs against RFWD3 and either left untreated or treated with UV (30 J/m 2 ). PCNA was recovered under denaturing conditions via Strep-Tactin pull-down and analyzed by immunoblotting with the indicated antibodies. (B) U2OS cells or U2OS/FRT GFP-RFWD3 WT or catalytic inactive (C315A) cells were treated with the indicated siRNAs, transfected with either empty vector (EV) or Strep-HA-PCNA plasmids, and treated with doxycycline to induce expression of RFWD3. UV treatment and protein pull-down were performed as in (A). (C) U2OS cells were transfected with the indicated plasmids and then subjected to Strep-Tactin pull-down as in (A). (D) U2OS/FRT GFP-RFWD3 WT cells were treated with doxycycline and transfected with EV or Strep-HA-PCNA 24 h before lysis in denaturing buffer. Lysates were subjected to Strep-Tactin pull-down in denaturing conditions, washed, and incubated with USP2 (ubiquitin protease) and/or UPL1 (SUMO protease), as indicated. (E) U2OS cells or U2OS/FRT GFP-RFWD3 WT cells were transfected with either control (siCtrl) or RAD18 siRNAs. After 48 h, cells were transfected with either EV or Strep-HA-PCNA plasmids and treated with doxycycline to induce the expression RFWD3 WT. Then, cells were treated with UV for 4 h and processed for Strep-Tactin pull-down as described in (A). The asterisk denotes a non-specific band.

    Article Snippet: Rabbit polyclonal antibody anti RAD18 , Bethyl Laboratories , Cat#A301-340A; RRID: AB_937974.

    Techniques: Ubiquitin Proteomics, Activity Assay, Expressing, Transfection, Western Blot, Plasmid Preparation, Lysis, Incubation, Control

    Journal: Molecular Cell

    Article Title: The ubiquitin ligase RFWD3 is required for translesion DNA synthesis

    doi: 10.1016/j.molcel.2020.11.029

    Figure Lengend Snippet:

    Article Snippet: Rabbit polyclonal antibody anti RAD18 , Bethyl Laboratories , Cat#A301-340A; RRID: AB_937974.

    Techniques: Ubiquitin Proteomics, Recombinant, Mutagenesis, Staining, Magnetic Beads, Transfection, Sequencing, Software