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rpl7 antibody  (Bio-Techne corporation)


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    Bio-Techne corporation rpl7 antibody
    Rpl7 Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 92/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nb100-2269/RPL7+Antibody/custom%40nb100-2269%4038732249
    Average 92 stars, based on 9 article reviews
    rpl7 antibody - by Bioz Stars, 2026-10
    92/100 stars

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    Related Articles

    Western Blot:

    Article Title: TGF-β2 Induces Ribosome Activity, Alters Ribosome Composition and Inhibits IRES-Mediated Translation in Chondrocytes
    Article Snippet: ling technologies, D9C2, Danvers, MA, USA), anti-phospho-4E-BP1 Thr37/46 (Cell signaling technologies, 236B4), anti-GAPDH (Fitzgerald, 4G5, Compton, UK), anti-α-Tubulin clone (Sigma, B512), anti-RPL7 (Novus bio, NB100-2269, Littleton, CO, USA) or anti-Histone H3 (Abcam, 24834, Cambridge, UK). Secondary antibodies were rabbit anti-mouse ALP or goat anti-rabbit ALP (both from DAKO, Glostrup Kommune,

    Incubation:

    Article Title: TGF-β2 Induces Ribosome Activity, Alters Ribosome Composition and Inhibits IRES-Mediated Translation in Chondrocytes
    Article Snippet: ling technologies, D9C2, Danvers, MA, USA), anti-phospho-4E-BP1 Thr37/46 (Cell signaling technologies, 236B4), anti-GAPDH (Fitzgerald, 4G5, Compton, UK), anti-α-Tubulin clone (Sigma, B512), anti-RPL7 (Novus bio, NB100-2269, Littleton, CO, USA) or anti-Histone H3 (Abcam, 24834, Cambridge, UK). Secondary antibodies were rabbit anti-mouse ALP or goat anti-rabbit ALP (both from DAKO, Glostrup Kommune,

    Milk:

    Article Title: TGF-β2 Induces Ribosome Activity, Alters Ribosome Composition and Inhibits IRES-Mediated Translation in Chondrocytes
    Article Snippet: ling technologies, D9C2, Danvers, MA, USA), anti-phospho-4E-BP1 Thr37/46 (Cell signaling technologies, 236B4), anti-GAPDH (Fitzgerald, 4G5, Compton, UK), anti-α-Tubulin clone (Sigma, B512), anti-RPL7 (Novus bio, NB100-2269, Littleton, CO, USA) or anti-Histone H3 (Abcam, 24834, Cambridge, UK). Secondary antibodies were rabbit anti-mouse ALP or goat anti-rabbit ALP (both from DAKO, Glostrup Kommune,

    Blocking Assay:

    Article Title: TGF-β2 Induces Ribosome Activity, Alters Ribosome Composition and Inhibits IRES-Mediated Translation in Chondrocytes
    Article Snippet: ling technologies, D9C2, Danvers, MA, USA), anti-phospho-4E-BP1 Thr37/46 (Cell signaling technologies, 236B4), anti-GAPDH (Fitzgerald, 4G5, Compton, UK), anti-α-Tubulin clone (Sigma, B512), anti-RPL7 (Novus bio, NB100-2269, Littleton, CO, USA) or anti-Histone H3 (Abcam, 24834, Cambridge, UK). Secondary antibodies were rabbit anti-mouse ALP or goat anti-rabbit ALP (both from DAKO, Glostrup Kommune,



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    ( A, B ) Western blots of reciprocal co-IPs of endogenous CLUH, astrin, and kinastrin in HeLa cells. Two different antibodies have been used to pull down CLUH (1, 2). Asterisk marks IgG light chain. ( C ) Scheme of human SPAG5 cDNA with indicated UTRs and ORFs. Closeup shows positions of the uATG and ATG1–6 with surrounding Kozak sequences. ( D, E ) Western blots of HeLa cells overexpressing FLAG-tagged astrin constructs. Pan-actin was used as loading control. ( F ) Western blots of reciprocal co-IPs of endogenous CLUH and overexpressed FLAG-tagged astrin full length (ATG1-SPAG5) or a N-terminal deleted variant (Δ151-SPAG5) in WT and CLUH KO HeLa cells. Pan-actin was used as loading control for input samples. Asterisks indicate additional astrin bands appearing upon overexpression of the N-terminal deleted variant. ( G ) Confocal immunofluorescence pictures of HeLa cells overexpressing FLAG-tagged astrin-1 and astrin-2 (SPAG5), astrin-1 (ATG3 + 4 + 5 GGG -SPAG5) or astrin-2 (ATG1 GGG -SPAG5) alone stained for FLAG (green) and CLUH (red). DAPI was used to stain nuclei (blue). Small boxes in left corners show a ×4 magnified area of boxed regions. Scale bar, 10 µm. ( H ) Polysome profiling of HeLa cells chemically crosslinked with dithiobis succinimidyl propionate (DSP). At the top, absorbance profile at 254 nm of the fractions is shown with indicated peaks of 40S and 60S ribosomal subunits, 80S monosome and polysomes; at the bottom the corresponding western blots of the fractions are shown. <t>RPL7</t> was used as a marker for ribosomes. Figure 1—source data 1. Uncropped blots for . Figure 1—source data 2. Uncropped blots for . Figure 1—source data 3. Unedited blots for .
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    ( A, B ) Western blots of reciprocal co-IPs of endogenous CLUH, astrin, and kinastrin in HeLa cells. Two different antibodies have been used to pull down CLUH (1, 2). Asterisk marks IgG light chain. ( C ) Scheme of human SPAG5 cDNA with indicated UTRs and ORFs. Closeup shows positions of the uATG and ATG1–6 with surrounding Kozak sequences. ( D, E ) Western blots of HeLa cells overexpressing FLAG-tagged astrin constructs. Pan-actin was used as loading control. ( F ) Western blots of reciprocal co-IPs of endogenous CLUH and overexpressed FLAG-tagged astrin full length (ATG1-SPAG5) or a N-terminal deleted variant (Δ151-SPAG5) in WT and CLUH KO HeLa cells. Pan-actin was used as loading control for input samples. Asterisks indicate additional astrin bands appearing upon overexpression of the N-terminal deleted variant. ( G ) Confocal immunofluorescence pictures of HeLa cells overexpressing FLAG-tagged astrin-1 and astrin-2 (SPAG5), astrin-1 (ATG3 + 4 + 5 GGG -SPAG5) or astrin-2 (ATG1 GGG -SPAG5) alone stained for FLAG (green) and CLUH (red). DAPI was used to stain nuclei (blue). Small boxes in left corners show a ×4 magnified area of boxed regions. Scale bar, 10 µm. ( H ) Polysome profiling of HeLa cells chemically crosslinked with dithiobis succinimidyl propionate (DSP). At the top, absorbance profile at 254 nm of the fractions is shown with indicated peaks of 40S and 60S ribosomal subunits, 80S monosome and polysomes; at the bottom the corresponding western blots of the fractions are shown. <t>RPL7</t> was used as a marker for ribosomes. Figure 1—source data 1. Uncropped blots for . Figure 1—source data 2. Uncropped blots for . Figure 1—source data 3. Unedited blots for .
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    Image Search Results


    ( A, B ) Western blots of reciprocal co-IPs of endogenous CLUH, astrin, and kinastrin in HeLa cells. Two different antibodies have been used to pull down CLUH (1, 2). Asterisk marks IgG light chain. ( C ) Scheme of human SPAG5 cDNA with indicated UTRs and ORFs. Closeup shows positions of the uATG and ATG1–6 with surrounding Kozak sequences. ( D, E ) Western blots of HeLa cells overexpressing FLAG-tagged astrin constructs. Pan-actin was used as loading control. ( F ) Western blots of reciprocal co-IPs of endogenous CLUH and overexpressed FLAG-tagged astrin full length (ATG1-SPAG5) or a N-terminal deleted variant (Δ151-SPAG5) in WT and CLUH KO HeLa cells. Pan-actin was used as loading control for input samples. Asterisks indicate additional astrin bands appearing upon overexpression of the N-terminal deleted variant. ( G ) Confocal immunofluorescence pictures of HeLa cells overexpressing FLAG-tagged astrin-1 and astrin-2 (SPAG5), astrin-1 (ATG3 + 4 + 5 GGG -SPAG5) or astrin-2 (ATG1 GGG -SPAG5) alone stained for FLAG (green) and CLUH (red). DAPI was used to stain nuclei (blue). Small boxes in left corners show a ×4 magnified area of boxed regions. Scale bar, 10 µm. ( H ) Polysome profiling of HeLa cells chemically crosslinked with dithiobis succinimidyl propionate (DSP). At the top, absorbance profile at 254 nm of the fractions is shown with indicated peaks of 40S and 60S ribosomal subunits, 80S monosome and polysomes; at the bottom the corresponding western blots of the fractions are shown. RPL7 was used as a marker for ribosomes. Figure 1—source data 1. Uncropped blots for . Figure 1—source data 2. Uncropped blots for . Figure 1—source data 3. Unedited blots for .

    Journal: eLife

    Article Title: CLUH controls astrin-1 expression to couple mitochondrial metabolism to cell cycle progression

    doi: 10.7554/eLife.74552

    Figure Lengend Snippet: ( A, B ) Western blots of reciprocal co-IPs of endogenous CLUH, astrin, and kinastrin in HeLa cells. Two different antibodies have been used to pull down CLUH (1, 2). Asterisk marks IgG light chain. ( C ) Scheme of human SPAG5 cDNA with indicated UTRs and ORFs. Closeup shows positions of the uATG and ATG1–6 with surrounding Kozak sequences. ( D, E ) Western blots of HeLa cells overexpressing FLAG-tagged astrin constructs. Pan-actin was used as loading control. ( F ) Western blots of reciprocal co-IPs of endogenous CLUH and overexpressed FLAG-tagged astrin full length (ATG1-SPAG5) or a N-terminal deleted variant (Δ151-SPAG5) in WT and CLUH KO HeLa cells. Pan-actin was used as loading control for input samples. Asterisks indicate additional astrin bands appearing upon overexpression of the N-terminal deleted variant. ( G ) Confocal immunofluorescence pictures of HeLa cells overexpressing FLAG-tagged astrin-1 and astrin-2 (SPAG5), astrin-1 (ATG3 + 4 + 5 GGG -SPAG5) or astrin-2 (ATG1 GGG -SPAG5) alone stained for FLAG (green) and CLUH (red). DAPI was used to stain nuclei (blue). Small boxes in left corners show a ×4 magnified area of boxed regions. Scale bar, 10 µm. ( H ) Polysome profiling of HeLa cells chemically crosslinked with dithiobis succinimidyl propionate (DSP). At the top, absorbance profile at 254 nm of the fractions is shown with indicated peaks of 40S and 60S ribosomal subunits, 80S monosome and polysomes; at the bottom the corresponding western blots of the fractions are shown. RPL7 was used as a marker for ribosomes. Figure 1—source data 1. Uncropped blots for . Figure 1—source data 2. Uncropped blots for . Figure 1—source data 3. Unedited blots for .

    Article Snippet: The following primary antibodies were used for western blotting: rabbit polyclonal anti-CLUH antibodies [detecting human CLUH; #NB100-93305 (1), #NB100-93306 (2)], rabbit polyclonal anti-RPS6 (#NB100-1595), rabbit polyclonal anti-RPL7 (#NB100-2269) antibodies from Novus Biologicals; rabbit polyclonal anti-astrin (#14726-1-AP) antibody from ProteinTech; rabbit polyclonal anti-FLAG (#F7425) and mouse monoclonal anti-FLAG (#F3165) antibodies from Sigma-Aldrich; mouse monoclonal pan-actin (#MAB1501) and anti-GAPDH (#MAB374) antibodies from EMD Millipore; rabbit polyclonal anti-CLUH antibody (detecting murine CLUH; #ARP70642_P050) from Aviva; rabbit polyclonal anti-kinastrin (#ab122769) and rabbit polyclonal pH3-Ser10 (#ab5176) antibodies from Abcam; mouse monoclonal anti-SDHA (#459200), anti-NDUFA9 (#459100), and anti-UQCRC1 (#459140) from Molecular probes; rabbit polyclonal pRB1-Ser807/811 (#9308), rabbit monoclonal pCDK1-Tyr15 (#4539), mouse monoclonal anti-cyclin D3 (#2936), and rabbit polyclonal pRPS6-Ser235/236 (#2211) antibodies from Cell Signaling and mouse monoclonal anti-CDK1 (#sc-54) antibody from Santa Cruz Biotechnologies.

    Techniques: Western Blot, Construct, Control, Variant Assay, Over Expression, Immunofluorescence, Staining, Marker

    Journal: eLife

    Article Title: CLUH controls astrin-1 expression to couple mitochondrial metabolism to cell cycle progression

    doi: 10.7554/eLife.74552

    Figure Lengend Snippet:

    Article Snippet: The following primary antibodies were used for western blotting: rabbit polyclonal anti-CLUH antibodies [detecting human CLUH; #NB100-93305 (1), #NB100-93306 (2)], rabbit polyclonal anti-RPS6 (#NB100-1595), rabbit polyclonal anti-RPL7 (#NB100-2269) antibodies from Novus Biologicals; rabbit polyclonal anti-astrin (#14726-1-AP) antibody from ProteinTech; rabbit polyclonal anti-FLAG (#F7425) and mouse monoclonal anti-FLAG (#F3165) antibodies from Sigma-Aldrich; mouse monoclonal pan-actin (#MAB1501) and anti-GAPDH (#MAB374) antibodies from EMD Millipore; rabbit polyclonal anti-CLUH antibody (detecting murine CLUH; #ARP70642_P050) from Aviva; rabbit polyclonal anti-kinastrin (#ab122769) and rabbit polyclonal pH3-Ser10 (#ab5176) antibodies from Abcam; mouse monoclonal anti-SDHA (#459200), anti-NDUFA9 (#459100), and anti-UQCRC1 (#459140) from Molecular probes; rabbit polyclonal pRB1-Ser807/811 (#9308), rabbit monoclonal pCDK1-Tyr15 (#4539), mouse monoclonal anti-cyclin D3 (#2936), and rabbit polyclonal pRPS6-Ser235/236 (#2211) antibodies from Cell Signaling and mouse monoclonal anti-CDK1 (#sc-54) antibody from Santa Cruz Biotechnologies.

    Techniques: CRISPR, Expressing, Derivative Assay, Selection, Recombinant, Plasmid Preparation, Construct, Control, Transfection, Sequencing, cDNA Synthesis