flow meter model t402 Search Results


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Millipore paclitaxel (t402)
(A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of <t>paclitaxel</t> (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).
Paclitaxel (T402), supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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(A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of <t>paclitaxel</t> (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).
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(A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of <t>paclitaxel</t> (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).
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(A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of <t>paclitaxel</t> (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).
Powerlab, supplied by ADInstruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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(A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of <t>paclitaxel</t> (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).
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GenScript corporation anti-phospho-t402-srebp-1 antibody
(A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of <t>paclitaxel</t> (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).
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Image Search Results


(A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of paclitaxel (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).

Journal: PLoS ONE

Article Title: The role of the MAD2-TLR4-MyD88 axis in paclitaxel resistance in ovarian cancer

doi: 10.1371/journal.pone.0243715

Figure Lengend Snippet: (A) Representative images of untransfected SKOV-3 cells and SKOV-3 cells transfected with siRNA targeting MAD2 (MAD2 siRNA) or a scrambled negative control siRNA (Scr siRNA) for 72 hours. After 24 hours, cells were either left untreated (-PTX) (a-c) or were treated with a 1μM dose of paclitaxel (+PTX) (d-f) for a further 48 hours. (B) Representative images of SKOV-3 cells stained using the senescence β-galactosidase staining kit following transfection for 72 hours (a-c) or 120 hours (d-f). (C) CCK-8 assay results. % cell viability for each condition was calculated as a percentage of untransfected SKOV-3 cells which were left untreated. The results demonstrate that knockdown of MAD2 renders SKOV-3 cells resistant to paclitaxel. (D) The percentage of β-galactosidase positive cells was calculated for each condition for (n = 3) technical and (n = 3) biological replicates. Following transfection a 3-fold increase in β-galactosidase expression was observed demonstrating that knockdown of MAD2 induces cellular senescence in SKOV-3 cells. (E) Trypan blue exclusion assay. (F) CCK-8 assay results for SKOV-3 cells treated with 200μM carboplatin for 48 hours following a 24 hour transfection. Results are expressed as mean +/-SD, n = 3. *p<0.05, **p<0.01, ***p<0.001 (Student’s t-test).

Article Snippet: Carboplatin (C2538), Paclitaxel (T402) and DMSO (D2650) were purchased from Sigma Aldrich.

Techniques: Transfection, Negative Control, Staining, CCK-8 Assay, Expressing, Trypan Blue Exclusion Assay