Review



ary013  (R&D Systems)


Bioz Verified Symbol R&D Systems is a verified supplier
Bioz Manufacturer Symbol R&D Systems manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 94

    Structured Review

    R&D Systems ary013
    Ary013, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 72 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ary013/product/R&D Systems
    Average 94 stars, based on 72 article reviews
    ary013 - by Bioz Stars, 2026-02
    94/100 stars

    Images



    Similar Products

    94
    R&D Systems ary013
    Ary013, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ary013/product/R&D Systems
    Average 94 stars, based on 1 article reviews
    ary013 - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    95
    Bio-Techne corporation proteome profiler mouse adipokine array kit
    Proteome Profiler Mouse Adipokine Array Kit, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/proteome profiler mouse adipokine array kit/product/Bio-Techne corporation
    Average 95 stars, based on 1 article reviews
    proteome profiler mouse adipokine array kit - by Bioz Stars, 2026-02
    95/100 stars
      Buy from Supplier

    93
    R&D Systems human adipokine array
    Human Adipokine Array, supplied by R&D Systems, 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/human adipokine array/product/R&D Systems
    Average 93 stars, based on 1 article reviews
    human adipokine array - by Bioz Stars, 2026-02
    93/100 stars
      Buy from Supplier

    93
    R&D Systems independent human adipokine arrays
    Independent Human Adipokine Arrays, supplied by R&D Systems, 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/independent human adipokine arrays/product/R&D Systems
    Average 93 stars, based on 1 article reviews
    independent human adipokine arrays - by Bioz Stars, 2026-02
    93/100 stars
      Buy from Supplier

    94
    R&D Systems proteome profiler mouse adipokine array kit
    Changes, especially browning, in the expression of proteins about adipocyte metabolism in marrow induced by AC-gelatin composites. (A) Fluorescence colocalization imaging of the UCP1 + adipocytes through represented by UCP1 and Plin (white triangles); all scale bars are 200 μm. (B) MAT browning promotion by AC-gelatin at 5 weeks in statistics of Fig. A. (C) Protein expression tests of osteo-organoid and bone marrow by Western blotting; β-tubulin, a protein expressed stably in adipocytes, was used as the internal reference. (D) Protein expression tests of whole marrow by protein microarray <t>(Proteome</t> Profiler Mouse <t>Adipokine</t> Array Kit, R&D Systems) and the quantified data (E). Error bars: mean ± SD; n = 2 (Fig. E, number of wells) or 3 (the others, number of mice); * p < 0.05, ** p < 0.01, **** p < 0.0001, two-way ANOVA.
    Proteome Profiler Mouse Adipokine Array Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/proteome profiler mouse adipokine array kit/product/R&D Systems
    Average 94 stars, based on 1 article reviews
    proteome profiler mouse adipokine array kit - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    93
    R&D Systems proteome profiler adipokine array
    IGF1 is elevated in coculture and regulates ECM gene expression and alternative NF-κB. A, Representative <t>adipokine</t> secretory profiles from ACI-23: preadipocyte cocultures and monoculture controls in complete media. B, Quantification of IGFBPs from adipokine arrays. One-way ANOVA with Tukey post hoc test ( n = 4). C, IGF1 ELISA of supernatants from 6-day preadipocyte and cancer cell cocultures, with monoculture controls in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). D, IGF1 ELISA of supernatants from preadipocyte and cancer cell cocultures, with monoculture controls used for RNA sequencing, all in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). E, Gene expression of IGF1 (top) and IGF2 (bottom) in primary and omental tumors from three publicly available data sets relativized to the average of the primary tumors. Unpaired t test. F, ECM gene expression via qRT-PCR of ACI-23 cells treated with 100-ng/mL IGF1 for 72 hours in complete media; data are fold change of vehicle. Unpaired t test ( n = 3–5). G, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with vehicle control or 100-ng/mL IGF1 for 4, 24, 48, and 72 hours in complete media. One-way ANOVA with Tukey post hoc ( n = 3). H, Gene expression of RELA and RELB in ACI-23 treated with vehicle control or 100-ng/mL IGF1 for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). I, RelB expression in cytosolic and nuclear fractions of ACI-23 cells treated with IGF1 for 72 hours in SFM. Lysate fractions were run on the same gel but displayed as separate panels for clarity. Western blots were also probed for nuclear and cytosolic housekeeping proteins lamin A/C, GAPDH, and α-tubulin ( n = 2). J, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with SFM or CM for 4, 24, 48, and 72 hours. One-way ANOVA with Tukey post hoc ( n = 3). K, Gene expression of RELA and RELB in ACI-23 cocultured with preadipocytes for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). *, P < 0.05; **, P < 0.01; ****, P < 0.0001; ns, not significant.
    Proteome Profiler Adipokine Array, supplied by R&D Systems, 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/proteome profiler adipokine array/product/R&D Systems
    Average 93 stars, based on 1 article reviews
    proteome profiler adipokine array - by Bioz Stars, 2026-02
    93/100 stars
      Buy from Supplier

    94
    R&D Systems proteome profiler mouse adipokine array kit ary013
    IGF1 is elevated in coculture and regulates ECM gene expression and alternative NF-κB. A, Representative <t>adipokine</t> secretory profiles from ACI-23: preadipocyte cocultures and monoculture controls in complete media. B, Quantification of IGFBPs from adipokine arrays. One-way ANOVA with Tukey post hoc test ( n = 4). C, IGF1 ELISA of supernatants from 6-day preadipocyte and cancer cell cocultures, with monoculture controls in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). D, IGF1 ELISA of supernatants from preadipocyte and cancer cell cocultures, with monoculture controls used for RNA sequencing, all in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). E, Gene expression of IGF1 (top) and IGF2 (bottom) in primary and omental tumors from three publicly available data sets relativized to the average of the primary tumors. Unpaired t test. F, ECM gene expression via qRT-PCR of ACI-23 cells treated with 100-ng/mL IGF1 for 72 hours in complete media; data are fold change of vehicle. Unpaired t test ( n = 3–5). G, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with vehicle control or 100-ng/mL IGF1 for 4, 24, 48, and 72 hours in complete media. One-way ANOVA with Tukey post hoc ( n = 3). H, Gene expression of RELA and RELB in ACI-23 treated with vehicle control or 100-ng/mL IGF1 for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). I, RelB expression in cytosolic and nuclear fractions of ACI-23 cells treated with IGF1 for 72 hours in SFM. Lysate fractions were run on the same gel but displayed as separate panels for clarity. Western blots were also probed for nuclear and cytosolic housekeeping proteins lamin A/C, GAPDH, and α-tubulin ( n = 2). J, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with SFM or CM for 4, 24, 48, and 72 hours. One-way ANOVA with Tukey post hoc ( n = 3). K, Gene expression of RELA and RELB in ACI-23 cocultured with preadipocytes for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). *, P < 0.05; **, P < 0.01; ****, P < 0.0001; ns, not significant.
    Proteome Profiler Mouse Adipokine Array Kit Ary013, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/proteome profiler mouse adipokine array kit ary013/product/R&D Systems
    Average 94 stars, based on 1 article reviews
    proteome profiler mouse adipokine array kit ary013 - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    94
    R&D Systems adipokine array kit mouse proteome profiler
    IGF1 is elevated in coculture and regulates ECM gene expression and alternative NF-κB. A, Representative <t>adipokine</t> secretory profiles from ACI-23: preadipocyte cocultures and monoculture controls in complete media. B, Quantification of IGFBPs from adipokine arrays. One-way ANOVA with Tukey post hoc test ( n = 4). C, IGF1 ELISA of supernatants from 6-day preadipocyte and cancer cell cocultures, with monoculture controls in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). D, IGF1 ELISA of supernatants from preadipocyte and cancer cell cocultures, with monoculture controls used for RNA sequencing, all in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). E, Gene expression of IGF1 (top) and IGF2 (bottom) in primary and omental tumors from three publicly available data sets relativized to the average of the primary tumors. Unpaired t test. F, ECM gene expression via qRT-PCR of ACI-23 cells treated with 100-ng/mL IGF1 for 72 hours in complete media; data are fold change of vehicle. Unpaired t test ( n = 3–5). G, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with vehicle control or 100-ng/mL IGF1 for 4, 24, 48, and 72 hours in complete media. One-way ANOVA with Tukey post hoc ( n = 3). H, Gene expression of RELA and RELB in ACI-23 treated with vehicle control or 100-ng/mL IGF1 for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). I, RelB expression in cytosolic and nuclear fractions of ACI-23 cells treated with IGF1 for 72 hours in SFM. Lysate fractions were run on the same gel but displayed as separate panels for clarity. Western blots were also probed for nuclear and cytosolic housekeeping proteins lamin A/C, GAPDH, and α-tubulin ( n = 2). J, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with SFM or CM for 4, 24, 48, and 72 hours. One-way ANOVA with Tukey post hoc ( n = 3). K, Gene expression of RELA and RELB in ACI-23 cocultured with preadipocytes for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). *, P < 0.05; **, P < 0.01; ****, P < 0.0001; ns, not significant.
    Adipokine Array Kit Mouse Proteome Profiler, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/adipokine array kit mouse proteome profiler/product/R&D Systems
    Average 94 stars, based on 1 article reviews
    adipokine array kit mouse proteome profiler - by Bioz Stars, 2026-02
    94/100 stars
      Buy from Supplier

    Image Search Results


    Changes, especially browning, in the expression of proteins about adipocyte metabolism in marrow induced by AC-gelatin composites. (A) Fluorescence colocalization imaging of the UCP1 + adipocytes through represented by UCP1 and Plin (white triangles); all scale bars are 200 μm. (B) MAT browning promotion by AC-gelatin at 5 weeks in statistics of Fig. A. (C) Protein expression tests of osteo-organoid and bone marrow by Western blotting; β-tubulin, a protein expressed stably in adipocytes, was used as the internal reference. (D) Protein expression tests of whole marrow by protein microarray (Proteome Profiler Mouse Adipokine Array Kit, R&D Systems) and the quantified data (E). Error bars: mean ± SD; n = 2 (Fig. E, number of wells) or 3 (the others, number of mice); * p < 0.05, ** p < 0.01, **** p < 0.0001, two-way ANOVA.

    Journal: Bioactive Materials

    Article Title: Amphiphilic cytokine traps remodel marrow adipose tissue for hematopoietic microenvironment amelioration

    doi: 10.1016/j.bioactmat.2024.08.032

    Figure Lengend Snippet: Changes, especially browning, in the expression of proteins about adipocyte metabolism in marrow induced by AC-gelatin composites. (A) Fluorescence colocalization imaging of the UCP1 + adipocytes through represented by UCP1 and Plin (white triangles); all scale bars are 200 μm. (B) MAT browning promotion by AC-gelatin at 5 weeks in statistics of Fig. A. (C) Protein expression tests of osteo-organoid and bone marrow by Western blotting; β-tubulin, a protein expressed stably in adipocytes, was used as the internal reference. (D) Protein expression tests of whole marrow by protein microarray (Proteome Profiler Mouse Adipokine Array Kit, R&D Systems) and the quantified data (E). Error bars: mean ± SD; n = 2 (Fig. E, number of wells) or 3 (the others, number of mice); * p < 0.05, ** p < 0.01, **** p < 0.0001, two-way ANOVA.

    Article Snippet: Changes, especially browning, in the expression of proteins about adipocyte metabolism in marrow induced by AC-gelatin composites. (A) Fluorescence colocalization imaging of the UCP1 + adipocytes through represented by UCP1 and Plin (white triangles); all scale bars are 200 μm. (B) MAT browning promotion by AC-gelatin at 5 weeks in statistics of Fig. A. (C) Protein expression tests of osteo-organoid and bone marrow by Western blotting; β-tubulin, a protein expressed stably in adipocytes, was used as the internal reference. (D) Protein expression tests of whole marrow by protein microarray (Proteome Profiler Mouse Adipokine Array Kit, R&D Systems) and the quantified data (E).

    Techniques: Expressing, Fluorescence, Imaging, Western Blot, Stable Transfection, Microarray

    IGF1 is elevated in coculture and regulates ECM gene expression and alternative NF-κB. A, Representative adipokine secretory profiles from ACI-23: preadipocyte cocultures and monoculture controls in complete media. B, Quantification of IGFBPs from adipokine arrays. One-way ANOVA with Tukey post hoc test ( n = 4). C, IGF1 ELISA of supernatants from 6-day preadipocyte and cancer cell cocultures, with monoculture controls in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). D, IGF1 ELISA of supernatants from preadipocyte and cancer cell cocultures, with monoculture controls used for RNA sequencing, all in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). E, Gene expression of IGF1 (top) and IGF2 (bottom) in primary and omental tumors from three publicly available data sets relativized to the average of the primary tumors. Unpaired t test. F, ECM gene expression via qRT-PCR of ACI-23 cells treated with 100-ng/mL IGF1 for 72 hours in complete media; data are fold change of vehicle. Unpaired t test ( n = 3–5). G, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with vehicle control or 100-ng/mL IGF1 for 4, 24, 48, and 72 hours in complete media. One-way ANOVA with Tukey post hoc ( n = 3). H, Gene expression of RELA and RELB in ACI-23 treated with vehicle control or 100-ng/mL IGF1 for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). I, RelB expression in cytosolic and nuclear fractions of ACI-23 cells treated with IGF1 for 72 hours in SFM. Lysate fractions were run on the same gel but displayed as separate panels for clarity. Western blots were also probed for nuclear and cytosolic housekeeping proteins lamin A/C, GAPDH, and α-tubulin ( n = 2). J, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with SFM or CM for 4, 24, 48, and 72 hours. One-way ANOVA with Tukey post hoc ( n = 3). K, Gene expression of RELA and RELB in ACI-23 cocultured with preadipocytes for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). *, P < 0.05; **, P < 0.01; ****, P < 0.0001; ns, not significant.

    Journal: Cancer Research

    Article Title: Omental Preadipocytes Stimulate Matrix Remodeling and IGF Signaling to Support Ovarian Cancer Metastasis

    doi: 10.1158/0008-5472.CAN-23-2613

    Figure Lengend Snippet: IGF1 is elevated in coculture and regulates ECM gene expression and alternative NF-κB. A, Representative adipokine secretory profiles from ACI-23: preadipocyte cocultures and monoculture controls in complete media. B, Quantification of IGFBPs from adipokine arrays. One-way ANOVA with Tukey post hoc test ( n = 4). C, IGF1 ELISA of supernatants from 6-day preadipocyte and cancer cell cocultures, with monoculture controls in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). D, IGF1 ELISA of supernatants from preadipocyte and cancer cell cocultures, with monoculture controls used for RNA sequencing, all in complete media. Two-way ANOVA with Sidak post hoc test ( n = 3). E, Gene expression of IGF1 (top) and IGF2 (bottom) in primary and omental tumors from three publicly available data sets relativized to the average of the primary tumors. Unpaired t test. F, ECM gene expression via qRT-PCR of ACI-23 cells treated with 100-ng/mL IGF1 for 72 hours in complete media; data are fold change of vehicle. Unpaired t test ( n = 3–5). G, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with vehicle control or 100-ng/mL IGF1 for 4, 24, 48, and 72 hours in complete media. One-way ANOVA with Tukey post hoc ( n = 3). H, Gene expression of RELA and RELB in ACI-23 treated with vehicle control or 100-ng/mL IGF1 for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). I, RelB expression in cytosolic and nuclear fractions of ACI-23 cells treated with IGF1 for 72 hours in SFM. Lysate fractions were run on the same gel but displayed as separate panels for clarity. Western blots were also probed for nuclear and cytosolic housekeeping proteins lamin A/C, GAPDH, and α-tubulin ( n = 2). J, NF-κB activity in OVCAR8-NF-κB-Luc cells treated with SFM or CM for 4, 24, 48, and 72 hours. One-way ANOVA with Tukey post hoc ( n = 3). K, Gene expression of RELA and RELB in ACI-23 cocultured with preadipocytes for 72 hours in complete media measured via qRT-PCR. Unpaired t test ( n = 3). *, P < 0.05; **, P < 0.01; ****, P < 0.0001; ns, not significant.

    Article Snippet: Secreted factors from cocultures and monoculture controls were measured using the Proteome Profiler Adipokine Array (ARY024) from R&D Systems according to manufacturer’s instructions.

    Techniques: Expressing, Enzyme-linked Immunosorbent Assay, RNA Sequencing Assay, Quantitative RT-PCR, Activity Assay, Control, Western Blot