canx Thermo Fisher Search Results


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  • 80
    Thermo Fisher gene exp canx mm00500330 m1
    Gene Exp Canx Mm00500330 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 80/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher gene exp canx rn00596877 m1
    Gene Exp Canx Rn00596877 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 78/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher gene exp canx hs01558409 m1
    Gene Exp Canx Hs01558409 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 79/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher sheep canx
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    Thermo Fisher calnexin canx cdna
    A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and <t>Calnexin</t> <t>(CANX)</t> when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts
    Calnexin Canx Cdna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 77/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher gene exp canx rn01459976 m1
    A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and <t>Calnexin</t> <t>(CANX)</t> when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts
    Gene Exp Canx Rn01459976 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 79/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher gene exp canx mm00626988 m1
    A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and <t>Calnexin</t> <t>(CANX)</t> when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts
    Gene Exp Canx Mm00626988 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 77/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher polyclonal rabbit cnx antibody
    A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and <t>Calnexin</t> <t>(CANX)</t> when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts
    Polyclonal Rabbit Cnx Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 79/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher cnx specific on target plus smartpool sirna
    A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and <t>Calnexin</t> <t>(CANX)</t> when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts
    Cnx Specific On Target Plus Smartpool Sirna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 79/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher anti calnexin cnx antibody
    A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and <t>Calnexin</t> <t>(CANX)</t> when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts
    Anti Calnexin Cnx Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 80/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher calnexin
    Estrogen and progesterone induce a unique transcriptomic response in ZR-75-1 and T-47D cells. a Protein steady state levels of ERα, PR-A, PR-B, androgen receptor (AR), androgen and progesterone regulated gene FKBP5 and estrogen regulated gene CTSD in ZR-75-1, T-47D and MCF-7 cells treated with ethanol (v.c.), 10nM DHT, 10nM PROG or 10nM estrogen for 16 h. TUBA and <t>calnexin</t> (CANX) were utilised as controls. Note that exposure time was different for each cell line and was optimised to visualise changes in response to hormone treatment. b Non hormone treated protein steady state levels of ERα, PR-A and PR-B in ZR-75-1, T-47D and MCF-7 cells treated with v.c. for 16 h. Alpha tubulin (TUBA) was utilised as a control. Exposure times were different from the blot presented in Fig. 1a. c Microarray analysis of the transcriptomic response of ZR-75-1 cells treated with ethanol (v.c.), 10 nM estrogen, 10 nM PROG, or cotreated with 10 nM estrogen and 10 nM PROG for 16 h. Euler diagram (left) demonstrates commonly regulated genes and those uniquely regulated by the hormonal cotreatment. Histograms (right) demonstrate validation of progesterone-regulated responses in independent samples. Expression presented relative to housekeeping gene GAPDH expression ( d ) Microarray analysis of the transcriptomic response of T-47D cells treated with ethanol (v.c.), 10 nM estrogen, 10 nM PROG, or cotreated with 10 nM estrogen and 10 nM PROG for 16 h. Euler diagram (left) demonstrates commonly regulated genes in response to each treatment. Histograms (right) demonstrate validation of progesterone-regulated responses in independent samples. e Cell cycle analysis of propidium iodide stained ZR-75-1 cells after treatment for 24 h with vehicle (V.C; ethanol), 10nM progesterone or pretreated for 72 h with 10nM estrogen (E2p), followed by 16 or 24 h of 10nM progesterone treatment (E2p + P4)
    Calnexin, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 336 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    CD160 Monoclonal Antibody for Western Blot Flow
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    PCNXL4 Polyclonal Antibody for Western Blot IF ICC IHC
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    Image Search Results


    A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and Calnexin (CANX) when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts

    Journal: Cell Biochemistry and Function

    Article Title: Protein Disulfide Isomerase Chaperone ERP-57 Decreases Plasma Membrane Expression of the Human GnRH Receptor

    doi: 10.1002/cbf.1622

    Figure Lengend Snippet: A dose response curve was elaborated in order to evidence the most dramatic and significant IP production restriction by the chaperones ERP-57 and Calnexin (CANX) when cotransfected with hWT GnRHR (25ng). Co-transfection of CANX or ERP-57 cDNAs restricts

    Article Snippet: ERP-57, ERP-72 and Calnexin (CANX) cDNA was obtained from Open Biosystems (Huntsville, Al. MHS1011-9199116, MHS1011-75436 and MHS1011-60083, respectively).

    Techniques: Cotransfection

    Estrogen and progesterone induce a unique transcriptomic response in ZR-75-1 and T-47D cells. a Protein steady state levels of ERα, PR-A, PR-B, androgen receptor (AR), androgen and progesterone regulated gene FKBP5 and estrogen regulated gene CTSD in ZR-75-1, T-47D and MCF-7 cells treated with ethanol (v.c.), 10nM DHT, 10nM PROG or 10nM estrogen for 16 h. TUBA and calnexin (CANX) were utilised as controls. Note that exposure time was different for each cell line and was optimised to visualise changes in response to hormone treatment. b Non hormone treated protein steady state levels of ERα, PR-A and PR-B in ZR-75-1, T-47D and MCF-7 cells treated with v.c. for 16 h. Alpha tubulin (TUBA) was utilised as a control. Exposure times were different from the blot presented in Fig. 1a. c Microarray analysis of the transcriptomic response of ZR-75-1 cells treated with ethanol (v.c.), 10 nM estrogen, 10 nM PROG, or cotreated with 10 nM estrogen and 10 nM PROG for 16 h. Euler diagram (left) demonstrates commonly regulated genes and those uniquely regulated by the hormonal cotreatment. Histograms (right) demonstrate validation of progesterone-regulated responses in independent samples. Expression presented relative to housekeeping gene GAPDH expression ( d ) Microarray analysis of the transcriptomic response of T-47D cells treated with ethanol (v.c.), 10 nM estrogen, 10 nM PROG, or cotreated with 10 nM estrogen and 10 nM PROG for 16 h. Euler diagram (left) demonstrates commonly regulated genes in response to each treatment. Histograms (right) demonstrate validation of progesterone-regulated responses in independent samples. e Cell cycle analysis of propidium iodide stained ZR-75-1 cells after treatment for 24 h with vehicle (V.C; ethanol), 10nM progesterone or pretreated for 72 h with 10nM estrogen (E2p), followed by 16 or 24 h of 10nM progesterone treatment (E2p + P4)

    Journal: BMC Cancer

    Article Title: The unique transcriptional response produced by concurrent estrogen and progesterone treatment in breast cancer cells results in upregulation of growth factor pathways and switching from a Luminal A to a Basal-like subtype

    doi: 10.1186/s12885-015-1819-3

    Figure Lengend Snippet: Estrogen and progesterone induce a unique transcriptomic response in ZR-75-1 and T-47D cells. a Protein steady state levels of ERα, PR-A, PR-B, androgen receptor (AR), androgen and progesterone regulated gene FKBP5 and estrogen regulated gene CTSD in ZR-75-1, T-47D and MCF-7 cells treated with ethanol (v.c.), 10nM DHT, 10nM PROG or 10nM estrogen for 16 h. TUBA and calnexin (CANX) were utilised as controls. Note that exposure time was different for each cell line and was optimised to visualise changes in response to hormone treatment. b Non hormone treated protein steady state levels of ERα, PR-A and PR-B in ZR-75-1, T-47D and MCF-7 cells treated with v.c. for 16 h. Alpha tubulin (TUBA) was utilised as a control. Exposure times were different from the blot presented in Fig. 1a. c Microarray analysis of the transcriptomic response of ZR-75-1 cells treated with ethanol (v.c.), 10 nM estrogen, 10 nM PROG, or cotreated with 10 nM estrogen and 10 nM PROG for 16 h. Euler diagram (left) demonstrates commonly regulated genes and those uniquely regulated by the hormonal cotreatment. Histograms (right) demonstrate validation of progesterone-regulated responses in independent samples. Expression presented relative to housekeeping gene GAPDH expression ( d ) Microarray analysis of the transcriptomic response of T-47D cells treated with ethanol (v.c.), 10 nM estrogen, 10 nM PROG, or cotreated with 10 nM estrogen and 10 nM PROG for 16 h. Euler diagram (left) demonstrates commonly regulated genes in response to each treatment. Histograms (right) demonstrate validation of progesterone-regulated responses in independent samples. e Cell cycle analysis of propidium iodide stained ZR-75-1 cells after treatment for 24 h with vehicle (V.C; ethanol), 10nM progesterone or pretreated for 72 h with 10nM estrogen (E2p), followed by 16 or 24 h of 10nM progesterone treatment (E2p + P4)

    Article Snippet: Membranes were probed using AR-N20, PR-H190, ERα-HC20, CTSD-H75, FKBP5-H100 (Santa Cruz Biotechnology, CA), calnexin (CANX, Thermo Scientific, VIC, Australia), and anti-tubulin alpha (TUBA, Millipore, VIC, Australia) and detected as previously described [ ].

    Techniques: Microarray, Expressing, Cell Cycle Assay, Staining