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rabbit polyclonal pp4-19c  (Proteintech)


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    Structured Review

    Proteintech rabbit polyclonal pp4-19c
    (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) <t>PP4-19c</t> staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).
    Rabbit Polyclonal Pp4 19c, supplied by Proteintech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal pp4-19c/product/Proteintech
    Average 90 stars, based on 1 article reviews
    rabbit polyclonal pp4-19c - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression"

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    Journal: Cell reports

    doi: 10.1016/j.celrep.2024.113823

    (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) PP4-19c staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).
    Figure Legend Snippet: (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) PP4-19c staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).

    Techniques Used: Mutagenesis, Staining, Quantitative RT-PCR, Immunoprecipitation, Reverse Transcription Polymerase Chain Reaction, Generated

    (A,B) Relative Flfl levels in ctrl, Kin17 RNAi, and Kin17 rescue NBs. Dotted lines, NBs [identified by size and CD8-GFP expression (not shown)]; Scale bar, 5 μm; n = 3 biological replicates. (C,D) PP4-19c localization in Kin17 RNAi and flfln42 NBs. Dashed circles, NBs. Ase staining indicates nucleus. Scale bar, 5 μm; n ≥ 51 NBs. Data are presented as the mean ± 1 SD. *, p<0.05; ***, p<0.001, paired student’s t-test with the Bonferroni correction for (B) and unpaired student’s t-test with the Bonferroni correction for (D).
    Figure Legend Snippet: (A,B) Relative Flfl levels in ctrl, Kin17 RNAi, and Kin17 rescue NBs. Dotted lines, NBs [identified by size and CD8-GFP expression (not shown)]; Scale bar, 5 μm; n = 3 biological replicates. (C,D) PP4-19c localization in Kin17 RNAi and flfln42 NBs. Dashed circles, NBs. Ase staining indicates nucleus. Scale bar, 5 μm; n ≥ 51 NBs. Data are presented as the mean ± 1 SD. *, p<0.05; ***, p<0.001, paired student’s t-test with the Bonferroni correction for (B) and unpaired student’s t-test with the Bonferroni correction for (D).

    Techniques Used: Expressing, Staining

    (A,B) Localization of Mira in PP4-19c and Flfl RNAi NBs throughout the cell cycle. Inset, Mira localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 27 NBs. (C) IP of PP4-19c (left) and quantification of dephosphorylation of Mira phosho-Serine96 peptide by PP4 precipitates (right). n = 4 biological replicates. (D) Localization of RFP-Flfl in NBs. Arrowheads, mitotic spindle; Arrows, centrosome; Scale bar, 5 μm. (E,F) Localization of PP4-19c in ctrl and PP4-19c RNAi NBs. Inset, PP4-19c localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 61 NBs. (G,H) Localization of Mira in prophase NBs expressing V5-PACT or V5-Flfl-PACT. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 25 NBs. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, paired student’s t-test for (C), unpaired student’s t-test for (H), and unpaired Student’s t-test with the Bonferroni correction for (B, F). See also Figure S4.
    Figure Legend Snippet: (A,B) Localization of Mira in PP4-19c and Flfl RNAi NBs throughout the cell cycle. Inset, Mira localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 27 NBs. (C) IP of PP4-19c (left) and quantification of dephosphorylation of Mira phosho-Serine96 peptide by PP4 precipitates (right). n = 4 biological replicates. (D) Localization of RFP-Flfl in NBs. Arrowheads, mitotic spindle; Arrows, centrosome; Scale bar, 5 μm. (E,F) Localization of PP4-19c in ctrl and PP4-19c RNAi NBs. Inset, PP4-19c localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 61 NBs. (G,H) Localization of Mira in prophase NBs expressing V5-PACT or V5-Flfl-PACT. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 25 NBs. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, paired student’s t-test for (C), unpaired student’s t-test for (H), and unpaired Student’s t-test with the Bonferroni correction for (B, F). See also Figure S4.

    Techniques Used: De-Phosphorylation Assay, Expressing

    Key resources table
    Figure Legend Snippet: Key resources table

    Techniques Used: Binding Assay, Virus, Recombinant, Protease Inhibitor, Phosphatase Assay, SYBR Green Assay, Reverse Transcription Polymerase Chain Reaction, Plasmid Preparation, Software, Microscopy, Membrane, PCR Cloning



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    Proteintech rabbit polyclonal pp4-19c
    (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) <t>PP4-19c</t> staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).
    Rabbit Polyclonal Pp4 19c, supplied by Proteintech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal pp4-19c/product/Proteintech
    Average 90 stars, based on 1 article reviews
    rabbit polyclonal pp4-19c - by Bioz Stars, 2026-05
    90/100 stars
      Buy from Supplier

    93
    Proteintech rabbit polyclonal pp4 19c
    (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) <t>PP4-19c</t> staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).
    Rabbit Polyclonal Pp4 19c, 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
    https://www.bioz.com/result/rabbit polyclonal pp4 19c/product/Proteintech
    Average 93 stars, based on 1 article reviews
    rabbit polyclonal pp4 19c - by Bioz Stars, 2026-05
    93/100 stars
      Buy from Supplier

    Image Search Results


    (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) PP4-19c staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) PP4-19c staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).

    Article Snippet: ​ REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) Proteintech #10262-1-AP Rabbit monoclonal HA (IP: 1μg/mg; IF: 1:500; IB: 1:1000) Invitrogen #3724 Guinea Pig Ase (IF: 1:5000) Y.N.

    Techniques: Mutagenesis, Staining, Quantitative RT-PCR, Immunoprecipitation, Reverse Transcription Polymerase Chain Reaction, Generated

    (A,B) Relative Flfl levels in ctrl, Kin17 RNAi, and Kin17 rescue NBs. Dotted lines, NBs [identified by size and CD8-GFP expression (not shown)]; Scale bar, 5 μm; n = 3 biological replicates. (C,D) PP4-19c localization in Kin17 RNAi and flfln42 NBs. Dashed circles, NBs. Ase staining indicates nucleus. Scale bar, 5 μm; n ≥ 51 NBs. Data are presented as the mean ± 1 SD. *, p<0.05; ***, p<0.001, paired student’s t-test with the Bonferroni correction for (B) and unpaired student’s t-test with the Bonferroni correction for (D).

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: (A,B) Relative Flfl levels in ctrl, Kin17 RNAi, and Kin17 rescue NBs. Dotted lines, NBs [identified by size and CD8-GFP expression (not shown)]; Scale bar, 5 μm; n = 3 biological replicates. (C,D) PP4-19c localization in Kin17 RNAi and flfln42 NBs. Dashed circles, NBs. Ase staining indicates nucleus. Scale bar, 5 μm; n ≥ 51 NBs. Data are presented as the mean ± 1 SD. *, p<0.05; ***, p<0.001, paired student’s t-test with the Bonferroni correction for (B) and unpaired student’s t-test with the Bonferroni correction for (D).

    Article Snippet: ​ REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) Proteintech #10262-1-AP Rabbit monoclonal HA (IP: 1μg/mg; IF: 1:500; IB: 1:1000) Invitrogen #3724 Guinea Pig Ase (IF: 1:5000) Y.N.

    Techniques: Expressing, Staining

    (A,B) Localization of Mira in PP4-19c and Flfl RNAi NBs throughout the cell cycle. Inset, Mira localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 27 NBs. (C) IP of PP4-19c (left) and quantification of dephosphorylation of Mira phosho-Serine96 peptide by PP4 precipitates (right). n = 4 biological replicates. (D) Localization of RFP-Flfl in NBs. Arrowheads, mitotic spindle; Arrows, centrosome; Scale bar, 5 μm. (E,F) Localization of PP4-19c in ctrl and PP4-19c RNAi NBs. Inset, PP4-19c localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 61 NBs. (G,H) Localization of Mira in prophase NBs expressing V5-PACT or V5-Flfl-PACT. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 25 NBs. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, paired student’s t-test for (C), unpaired student’s t-test for (H), and unpaired Student’s t-test with the Bonferroni correction for (B, F). See also Figure S4.

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: (A,B) Localization of Mira in PP4-19c and Flfl RNAi NBs throughout the cell cycle. Inset, Mira localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 27 NBs. (C) IP of PP4-19c (left) and quantification of dephosphorylation of Mira phosho-Serine96 peptide by PP4 precipitates (right). n = 4 biological replicates. (D) Localization of RFP-Flfl in NBs. Arrowheads, mitotic spindle; Arrows, centrosome; Scale bar, 5 μm. (E,F) Localization of PP4-19c in ctrl and PP4-19c RNAi NBs. Inset, PP4-19c localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 61 NBs. (G,H) Localization of Mira in prophase NBs expressing V5-PACT or V5-Flfl-PACT. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 25 NBs. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, paired student’s t-test for (C), unpaired student’s t-test for (H), and unpaired Student’s t-test with the Bonferroni correction for (B, F). See also Figure S4.

    Article Snippet: ​ REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) Proteintech #10262-1-AP Rabbit monoclonal HA (IP: 1μg/mg; IF: 1:500; IB: 1:1000) Invitrogen #3724 Guinea Pig Ase (IF: 1:5000) Y.N.

    Techniques: De-Phosphorylation Assay, Expressing

    Key resources table

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: Key resources table

    Article Snippet: ​ REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) Proteintech #10262-1-AP Rabbit monoclonal HA (IP: 1μg/mg; IF: 1:500; IB: 1:1000) Invitrogen #3724 Guinea Pig Ase (IF: 1:5000) Y.N.

    Techniques: Binding Assay, Virus, Recombinant, Protease Inhibitor, Phosphatase Assay, SYBR Green Assay, Reverse Transcription Polymerase Chain Reaction, Plasmid Preparation, Software, Microscopy, Membrane, PCR Cloning

    (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) PP4-19c staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: (A,B) Localization of Mira throughout the cell cycle in u6atacK01105 (u6atac−/−) mutant and U2A RNAi NBs. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 19 NBs. (C,D) Cortical localization of Mira in metaphase u6atac−/− NBs. Arrows, basal cortex. Scale bar, 5 μm; n ≥ 19 NBs. (E,F) Pros nuclear localization in u6atac−/−mutant NBs. Dashed circles outline NBs. Scale bar, 5 μm; n ≥ 6 brains. (G,H) Mitotic Index in u6atac−/− mutant brains. Yellow circles, mitotic NBs; Grey circles, non-mitotic NBs; Scale bar, 20 μm; n ≥ 7 brains. (I,J) Flfl staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar, 10 μm; n = 3 biological replicates. (K) PP4-19c staining in u6atac−/− mutant NBs. Dashed circles, NBs; Scale bar. (L) Localization of Kin17-HA in NBs during interphase and mitosis. Scale bar, 5 μm. (M) Quantitative RT-PCR results for Flfl transcript. Left panel, position of primers. n = 8 biological replicates (N) RNA immunoprecipitation of flfl mRNA by Kin17-HA in Drosophila embryos. Top panel, IP of Kin17-HA proteins; Bottom panels, flfl RT-PCR products obtained from cDNA libraries generated from RIP immunoprecipitates. Lysate and IP samples were run on the same blot but images were taken from different exposures. (O) aPKC and Pros RT-PCR results obtained from cDNA libraries generated from RIP immunoprecipitates. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, unpaired student’s t-test with Bonferroni correction (B). unpaired Student’s t-test for (F, H), and paired Student’s t-test for (J).

    Article Snippet: Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) , Proteintech , #10262-1-AP.

    Techniques: Mutagenesis, Staining, Quantitative RT-PCR, RNA Immunoprecipitation, Reverse Transcription Polymerase Chain Reaction, Generated

    (A,B) Relative Flfl levels in ctrl, Kin17 RNAi, and Kin17 rescue NBs. Dotted lines, NBs [identified by size and CD8-GFP expression (not shown)]; Scale bar, 5 μm; n = 3 biological replicates. (C,D) PP4-19c localization in Kin17 RNAi and flfln42 NBs. Dashed circles, NBs. Ase staining indicates nucleus. Scale bar, 5 μm; n ≥ 51 NBs. Data are presented as the mean ± 1 SD. *, p<0.05; ***, p<0.001, paired student’s t-test with the Bonferroni correction for (B) and unpaired student’s t-test with the Bonferroni correction for (D).

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: (A,B) Relative Flfl levels in ctrl, Kin17 RNAi, and Kin17 rescue NBs. Dotted lines, NBs [identified by size and CD8-GFP expression (not shown)]; Scale bar, 5 μm; n = 3 biological replicates. (C,D) PP4-19c localization in Kin17 RNAi and flfln42 NBs. Dashed circles, NBs. Ase staining indicates nucleus. Scale bar, 5 μm; n ≥ 51 NBs. Data are presented as the mean ± 1 SD. *, p<0.05; ***, p<0.001, paired student’s t-test with the Bonferroni correction for (B) and unpaired student’s t-test with the Bonferroni correction for (D).

    Article Snippet: Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) , Proteintech , #10262-1-AP.

    Techniques: Expressing, Staining

    (A,B) Localization of Mira in PP4-19c and Flfl RNAi NBs throughout the cell cycle. Inset, Mira localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 27 NBs. (C) IP of PP4-19c (left) and quantification of dephosphorylation of Mira phosho-Serine96 peptide by PP4 precipitates (right). n = 4 biological replicates. (D) Localization of RFP-Flfl in NBs. Arrowheads, mitotic spindle; Arrows, centrosome; Scale bar, 5 μm. (E,F) Localization of PP4-19c in ctrl and PP4-19c RNAi NBs. Inset, PP4-19c localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 61 NBs. (G,H) Localization of Mira in prophase NBs expressing V5-PACT or V5-Flfl-PACT. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 25 NBs. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, paired student’s t-test for (C), unpaired student’s t-test for (H), and unpaired Student’s t-test with the Bonferroni correction for (B, F). See also Figure S4.

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: (A,B) Localization of Mira in PP4-19c and Flfl RNAi NBs throughout the cell cycle. Inset, Mira localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 27 NBs. (C) IP of PP4-19c (left) and quantification of dephosphorylation of Mira phosho-Serine96 peptide by PP4 precipitates (right). n = 4 biological replicates. (D) Localization of RFP-Flfl in NBs. Arrowheads, mitotic spindle; Arrows, centrosome; Scale bar, 5 μm. (E,F) Localization of PP4-19c in ctrl and PP4-19c RNAi NBs. Inset, PP4-19c localization at apical (yellow) and basal (grey) centrosomes; Scale bar, 5 μm; n ≥ 61 NBs. (G,H) Localization of Mira in prophase NBs expressing V5-PACT or V5-Flfl-PACT. Inset, Mira localization at apical (yellow boxes) and basal (grey boxes) centrosomes; Scale bar, 5 μm; n ≥ 25 NBs. Data are presented as the mean ± 1 SD. n.s., not significant; *, p<0.05; **, p<0.01; ***, p<0.001, paired student’s t-test for (C), unpaired student’s t-test for (H), and unpaired Student’s t-test with the Bonferroni correction for (B, F). See also Figure S4.

    Article Snippet: Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) , Proteintech , #10262-1-AP.

    Techniques: De-Phosphorylation Assay, Expressing

    Key resources table

    Journal: Cell reports

    Article Title: Kin17 regulates proper cortical localization of Miranda in Drosophila neuroblasts by regulating Flfl expression

    doi: 10.1016/j.celrep.2024.113823

    Figure Lengend Snippet: Key resources table

    Article Snippet: Rabbit polyclonal PP4-19c (IP: 4 μg/mg; IF: 1:1000; IB: 1:1000) , Proteintech , #10262-1-AP.

    Techniques: Binding Assay, Virus, Recombinant, Protease Inhibitor, Phosphatase Assay, SYBR Green Assay, One Step RT-PCR, Plasmid Preparation, Software, Microscopy, Membrane, Reverse Transcription, PCR Cloning