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ran activation assay sta-409  (Cell Biolabs Inc)

 
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    Structured Review

    Cell Biolabs Inc ran activation assay sta-409
    a Western blot analysis of HDAC8 in 32D-CM cells with NS or Hdac8 shRNA (#1, #2) (left). Relative expression of pre-miR-126 and mature miR-126 in 32D-CM cells with NS (red) vs. Hdac8 shRNA#1 (light blue), Hdac8 shRNA#2 (dark blue) (right). b Relative expression in 32D-CM cells treated with vehicle (red) vs. HDAC8i (22d 2.5 μM or 5 μM; purple) for pre-miR-126 (left; 2.5 μM p < 0.0001; 5 μM p < 0.0001) and miR-126 (right; 2.5 μM p = 0.012; 5 μM p = 0.0055). c Representative image of IF co-staining of <t>RAN</t> (green) and HDAC8 (red) in 32D cells (left; scale bar 10 μm). IP with anti-IgG control or anti-HDAC8 followed by immunoblotting (IB) with anti-RAN antibodies (right). Representative results of two independent experiments with similar results are shown. d IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN in 32D-CM cells not-treated (NT) or treated with DMSO vehicle or 22d (2 µM) (left). The levels of RAN-GTP determined by <t>RAN</t> <t>activation</t> assay (right). The densitometry of RAN-GTP levels measured from three assays are shown on the bottom. e IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) in 32D-CM cells not-treated (NT) or transduced with shCtrl control or shCM for 24 h. f IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) of BM cells isolated from Ctrl or CM mice. g Schematic model of the mechanism by which CM regulates miR-126/EGFL7 transcription as well as miR-126 biogenesis through enhancing HDAC8 activity which in turn promotes RAN-XPO5 mediated transportation. Pre-miR-126 was normalized to B2m and mature miR-126 was normalized to snoRNA234 . Data are presented as the mean ± SD and statistical significance shown was determined using two-tailed Student’s T tests (* p < 0.05; ** p < 0.01; *** p < 0.001).
    Ran Activation Assay Sta 409, supplied by Cell Biolabs Inc, 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/ran activation assay sta-409/product/Cell Biolabs Inc
    Average 90 stars, based on 1 article reviews
    ran activation assay sta-409 - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Targeting miR-126 in inv(16) acute myeloid leukemia inhibits leukemia development and leukemia stem cell maintenance"

    Article Title: Targeting miR-126 in inv(16) acute myeloid leukemia inhibits leukemia development and leukemia stem cell maintenance

    Journal: Nature Communications

    doi: 10.1038/s41467-021-26420-7

    a Western blot analysis of HDAC8 in 32D-CM cells with NS or Hdac8 shRNA (#1, #2) (left). Relative expression of pre-miR-126 and mature miR-126 in 32D-CM cells with NS (red) vs. Hdac8 shRNA#1 (light blue), Hdac8 shRNA#2 (dark blue) (right). b Relative expression in 32D-CM cells treated with vehicle (red) vs. HDAC8i (22d 2.5 μM or 5 μM; purple) for pre-miR-126 (left; 2.5 μM p < 0.0001; 5 μM p < 0.0001) and miR-126 (right; 2.5 μM p = 0.012; 5 μM p = 0.0055). c Representative image of IF co-staining of RAN (green) and HDAC8 (red) in 32D cells (left; scale bar 10 μm). IP with anti-IgG control or anti-HDAC8 followed by immunoblotting (IB) with anti-RAN antibodies (right). Representative results of two independent experiments with similar results are shown. d IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN in 32D-CM cells not-treated (NT) or treated with DMSO vehicle or 22d (2 µM) (left). The levels of RAN-GTP determined by RAN activation assay (right). The densitometry of RAN-GTP levels measured from three assays are shown on the bottom. e IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) in 32D-CM cells not-treated (NT) or transduced with shCtrl control or shCM for 24 h. f IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) of BM cells isolated from Ctrl or CM mice. g Schematic model of the mechanism by which CM regulates miR-126/EGFL7 transcription as well as miR-126 biogenesis through enhancing HDAC8 activity which in turn promotes RAN-XPO5 mediated transportation. Pre-miR-126 was normalized to B2m and mature miR-126 was normalized to snoRNA234 . Data are presented as the mean ± SD and statistical significance shown was determined using two-tailed Student’s T tests (* p < 0.05; ** p < 0.01; *** p < 0.001).
    Figure Legend Snippet: a Western blot analysis of HDAC8 in 32D-CM cells with NS or Hdac8 shRNA (#1, #2) (left). Relative expression of pre-miR-126 and mature miR-126 in 32D-CM cells with NS (red) vs. Hdac8 shRNA#1 (light blue), Hdac8 shRNA#2 (dark blue) (right). b Relative expression in 32D-CM cells treated with vehicle (red) vs. HDAC8i (22d 2.5 μM or 5 μM; purple) for pre-miR-126 (left; 2.5 μM p < 0.0001; 5 μM p < 0.0001) and miR-126 (right; 2.5 μM p = 0.012; 5 μM p = 0.0055). c Representative image of IF co-staining of RAN (green) and HDAC8 (red) in 32D cells (left; scale bar 10 μm). IP with anti-IgG control or anti-HDAC8 followed by immunoblotting (IB) with anti-RAN antibodies (right). Representative results of two independent experiments with similar results are shown. d IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN in 32D-CM cells not-treated (NT) or treated with DMSO vehicle or 22d (2 µM) (left). The levels of RAN-GTP determined by RAN activation assay (right). The densitometry of RAN-GTP levels measured from three assays are shown on the bottom. e IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) in 32D-CM cells not-treated (NT) or transduced with shCtrl control or shCM for 24 h. f IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) of BM cells isolated from Ctrl or CM mice. g Schematic model of the mechanism by which CM regulates miR-126/EGFL7 transcription as well as miR-126 biogenesis through enhancing HDAC8 activity which in turn promotes RAN-XPO5 mediated transportation. Pre-miR-126 was normalized to B2m and mature miR-126 was normalized to snoRNA234 . Data are presented as the mean ± SD and statistical significance shown was determined using two-tailed Student’s T tests (* p < 0.05; ** p < 0.01; *** p < 0.001).

    Techniques Used: Western Blot, shRNA, Expressing, Staining, Control, Activation Assay, Transduction, Isolation, Activity Assay, Two Tailed Test



    Similar Products

    ran activation assay sta-409  (Cell Biolabs Inc)
    90
    Cell Biolabs Inc ran activation assay sta-409
    a Western blot analysis of HDAC8 in 32D-CM cells with NS or Hdac8 shRNA (#1, #2) (left). Relative expression of pre-miR-126 and mature miR-126 in 32D-CM cells with NS (red) vs. Hdac8 shRNA#1 (light blue), Hdac8 shRNA#2 (dark blue) (right). b Relative expression in 32D-CM cells treated with vehicle (red) vs. HDAC8i (22d 2.5 μM or 5 μM; purple) for pre-miR-126 (left; 2.5 μM p < 0.0001; 5 μM p < 0.0001) and miR-126 (right; 2.5 μM p = 0.012; 5 μM p = 0.0055). c Representative image of IF co-staining of <t>RAN</t> (green) and HDAC8 (red) in 32D cells (left; scale bar 10 μm). IP with anti-IgG control or anti-HDAC8 followed by immunoblotting (IB) with anti-RAN antibodies (right). Representative results of two independent experiments with similar results are shown. d IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN in 32D-CM cells not-treated (NT) or treated with DMSO vehicle or 22d (2 µM) (left). The levels of RAN-GTP determined by <t>RAN</t> <t>activation</t> assay (right). The densitometry of RAN-GTP levels measured from three assays are shown on the bottom. e IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) in 32D-CM cells not-treated (NT) or transduced with shCtrl control or shCM for 24 h. f IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) of BM cells isolated from Ctrl or CM mice. g Schematic model of the mechanism by which CM regulates miR-126/EGFL7 transcription as well as miR-126 biogenesis through enhancing HDAC8 activity which in turn promotes RAN-XPO5 mediated transportation. Pre-miR-126 was normalized to B2m and mature miR-126 was normalized to snoRNA234 . Data are presented as the mean ± SD and statistical significance shown was determined using two-tailed Student’s T tests (* p < 0.05; ** p < 0.01; *** p < 0.001).
    Ran Activation Assay Sta 409, supplied by Cell Biolabs Inc, 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/ran activation assay sta-409/product/Cell Biolabs Inc
    Average 90 stars, based on 1 article reviews
    ran activation assay sta-409 - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier
    ran activation assay kit sta-409  (Cell Biolabs Inc)
    90
    Cell Biolabs Inc ran activation assay kit sta-409
    a Western blot analysis of HDAC8 in 32D-CM cells with NS or Hdac8 shRNA (#1, #2) (left). Relative expression of pre-miR-126 and mature miR-126 in 32D-CM cells with NS (red) vs. Hdac8 shRNA#1 (light blue), Hdac8 shRNA#2 (dark blue) (right). b Relative expression in 32D-CM cells treated with vehicle (red) vs. HDAC8i (22d 2.5 μM or 5 μM; purple) for pre-miR-126 (left; 2.5 μM p < 0.0001; 5 μM p < 0.0001) and miR-126 (right; 2.5 μM p = 0.012; 5 μM p = 0.0055). c Representative image of IF co-staining of <t>RAN</t> (green) and HDAC8 (red) in 32D cells (left; scale bar 10 μm). IP with anti-IgG control or anti-HDAC8 followed by immunoblotting (IB) with anti-RAN antibodies (right). Representative results of two independent experiments with similar results are shown. d IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN in 32D-CM cells not-treated (NT) or treated with DMSO vehicle or 22d (2 µM) (left). The levels of RAN-GTP determined by <t>RAN</t> <t>activation</t> assay (right). The densitometry of RAN-GTP levels measured from three assays are shown on the bottom. e IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) in 32D-CM cells not-treated (NT) or transduced with shCtrl control or shCM for 24 h. f IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) of BM cells isolated from Ctrl or CM mice. g Schematic model of the mechanism by which CM regulates miR-126/EGFL7 transcription as well as miR-126 biogenesis through enhancing HDAC8 activity which in turn promotes RAN-XPO5 mediated transportation. Pre-miR-126 was normalized to B2m and mature miR-126 was normalized to snoRNA234 . Data are presented as the mean ± SD and statistical significance shown was determined using two-tailed Student’s T tests (* p < 0.05; ** p < 0.01; *** p < 0.001).
    Ran Activation Assay Kit Sta 409, supplied by Cell Biolabs Inc, 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/ran activation assay kit sta-409/product/Cell Biolabs Inc
    Average 90 stars, based on 1 article reviews
    ran activation assay kit sta-409 - by Bioz Stars, 2026-05
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    a Western blot analysis of HDAC8 in 32D-CM cells with NS or Hdac8 shRNA (#1, #2) (left). Relative expression of pre-miR-126 and mature miR-126 in 32D-CM cells with NS (red) vs. Hdac8 shRNA#1 (light blue), Hdac8 shRNA#2 (dark blue) (right). b Relative expression in 32D-CM cells treated with vehicle (red) vs. HDAC8i (22d 2.5 μM or 5 μM; purple) for pre-miR-126 (left; 2.5 μM p < 0.0001; 5 μM p < 0.0001) and miR-126 (right; 2.5 μM p = 0.012; 5 μM p = 0.0055). c Representative image of IF co-staining of RAN (green) and HDAC8 (red) in 32D cells (left; scale bar 10 μm). IP with anti-IgG control or anti-HDAC8 followed by immunoblotting (IB) with anti-RAN antibodies (right). Representative results of two independent experiments with similar results are shown. d IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN in 32D-CM cells not-treated (NT) or treated with DMSO vehicle or 22d (2 µM) (left). The levels of RAN-GTP determined by RAN activation assay (right). The densitometry of RAN-GTP levels measured from three assays are shown on the bottom. e IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) in 32D-CM cells not-treated (NT) or transduced with shCtrl control or shCM for 24 h. f IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) of BM cells isolated from Ctrl or CM mice. g Schematic model of the mechanism by which CM regulates miR-126/EGFL7 transcription as well as miR-126 biogenesis through enhancing HDAC8 activity which in turn promotes RAN-XPO5 mediated transportation. Pre-miR-126 was normalized to B2m and mature miR-126 was normalized to snoRNA234 . Data are presented as the mean ± SD and statistical significance shown was determined using two-tailed Student’s T tests (* p < 0.05; ** p < 0.01; *** p < 0.001).

    Journal: Nature Communications

    Article Title: Targeting miR-126 in inv(16) acute myeloid leukemia inhibits leukemia development and leukemia stem cell maintenance

    doi: 10.1038/s41467-021-26420-7

    Figure Lengend Snippet: a Western blot analysis of HDAC8 in 32D-CM cells with NS or Hdac8 shRNA (#1, #2) (left). Relative expression of pre-miR-126 and mature miR-126 in 32D-CM cells with NS (red) vs. Hdac8 shRNA#1 (light blue), Hdac8 shRNA#2 (dark blue) (right). b Relative expression in 32D-CM cells treated with vehicle (red) vs. HDAC8i (22d 2.5 μM or 5 μM; purple) for pre-miR-126 (left; 2.5 μM p < 0.0001; 5 μM p < 0.0001) and miR-126 (right; 2.5 μM p = 0.012; 5 μM p = 0.0055). c Representative image of IF co-staining of RAN (green) and HDAC8 (red) in 32D cells (left; scale bar 10 μm). IP with anti-IgG control or anti-HDAC8 followed by immunoblotting (IB) with anti-RAN antibodies (right). Representative results of two independent experiments with similar results are shown. d IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN in 32D-CM cells not-treated (NT) or treated with DMSO vehicle or 22d (2 µM) (left). The levels of RAN-GTP determined by RAN activation assay (right). The densitometry of RAN-GTP levels measured from three assays are shown on the bottom. e IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) in 32D-CM cells not-treated (NT) or transduced with shCtrl control or shCM for 24 h. f IP with anti-RAN and IB with antibodies for Ac-Lys, RCC1, XPO5, or RAN (left), and RAN activation assay (right) of BM cells isolated from Ctrl or CM mice. g Schematic model of the mechanism by which CM regulates miR-126/EGFL7 transcription as well as miR-126 biogenesis through enhancing HDAC8 activity which in turn promotes RAN-XPO5 mediated transportation. Pre-miR-126 was normalized to B2m and mature miR-126 was normalized to snoRNA234 . Data are presented as the mean ± SD and statistical significance shown was determined using two-tailed Student’s T tests (* p < 0.05; ** p < 0.01; *** p < 0.001).

    Article Snippet: RAN activation assay (Cell Biolabs, STA-409) was performed to measure activities of RAN according to the manufacturer’s guidance.

    Techniques: Western Blot, shRNA, Expressing, Staining, Control, Activation Assay, Transduction, Isolation, Activity Assay, Two Tailed Test