human cd2 Search Results


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Miltenyi Biotec anti human cd2 microbeads
Anti Human Cd2 Microbeads, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Miltenyi Biotec cd2 apc rea1130 miltenyi biotec 130 119 509 cd3 bv421 sk7 biolegend 344834
Cd2 Apc Rea1130 Miltenyi Biotec 130 119 509 Cd3 Bv421 Sk7 Biolegend 344834, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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Miltenyi Biotec human cd2 hcd2 pevio770 lt2 antibodies
Figure 5. Virally induced constitutively active CD30 signaling results in more Cre-reporter+ cells within B cells. CAR//Cγ1-cre mice (dots) and LC30//Cγ1-cre mice (squares) were i.p. infected with MHV-68 hNGFR and splenic cells were analyzed 14 days post-infection. (A) Breeding scheme of LC30//Cγ1cre mice. The excision of the loxP-flanked stop cassette was followed by <t>hCD2</t> reporter expression (Cre-reporter) and ligand-independent constitutively active CD30 signaling. (B) The splenic
Human Cd2 Hcd2 Pevio770 Lt2 Antibodies, supplied by Miltenyi Biotec, 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/product/human+cd2/CD2+Antibody%2C+anti-human/pm38132100-92-5-14
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human cd2 hcd2 pevio770 lt2 antibodies - by Bioz Stars, 2026-10
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Miltenyi Biotec pan t isolation kit
Figure 5. Virally induced constitutively active CD30 signaling results in more Cre-reporter+ cells within B cells. CAR//Cγ1-cre mice (dots) and LC30//Cγ1-cre mice (squares) were i.p. infected with MHV-68 hNGFR and splenic cells were analyzed 14 days post-infection. (A) Breeding scheme of LC30//Cγ1cre mice. The excision of the loxP-flanked stop cassette was followed by <t>hCD2</t> reporter expression (Cre-reporter) and ligand-independent constitutively active CD30 signaling. (B) The splenic
Pan T Isolation Kit, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+cd2/CD2+MicroBeads%2C+non-human+primate/pmc06194331-95-15-20
Average 92 stars, based on 1 article reviews
pan t isolation kit - by Bioz Stars, 2026-10
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Miltenyi Biotec cd2
(A–C) FILM acquisition of binder probes that recognize <t>CD2,</t> ICAM-1 (CD54) in the pSMAC, and CD45 in the dSMAC zones (10 nm pixels with 3-pixel Gaussian blurring). For CD2 and CD45, APC-conjugated antibodies were used; for ICAM-1, a nanobody Fab conjugated with Vio ® 667 was used. Cyan boxed region shows the IF image (103.17 nm pixels) corresponding to the white boxed region. (D–F) Zoom-in of the respective boxed regions for the panels to the left. Localizations are shown as peak-normalized 2D Gaussians with color-coded precision according to the colorbar. (G–I) Zoom-in of the respective boxed regions for the panels to the immediate left. Localizations are shown as crosses (indicating ±1-σ uncertainty in x and y ) with color-coded precision according to the colorbar.
Cd2, supplied by Miltenyi Biotec, 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/product/human+cd2/CD2+Antibody%2C+anti-human%2C+REAfinity/bio_rxiv__64898__2025__12__16__694546-203-8-14
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cd2 - by Bioz Stars, 2026-10
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Elabscience Biotechnology apc anti human cd206 lw1218
Expression of CD86 (M1) and <t>CD206</t> (M2). (A) : Expression of CD86 (M1); (B) : Expression of CD206 (M2). # P < 0.05, ## P < 0.01 vs. sham; * p < 0.05, ** p < 0.01 vs. MCAO/R.
Apc Anti Human Cd206 Lw1218, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluidigm cd2

Cd2, supplied by fluidigm, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad anti human cd2

Anti Human Cd2, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MedChemExpress cs1
a Evaluation of the effects on EGR1 expression levels of 200 μM CuCl 2 (60 min treatment) following siRNA knockdown of various PTPs in A549 cells. Depicted are two interpretations of the results. ( top ) All fold-changes are reported relative to the negative control siRNA transfect (Neg.) without CuCl 2 supplementation. ( bottom ) Each result is reported as the fold-change between the denoted siRNA knockdown after 60 min 200 μM CuCl 2 supplementation and the siRNA knockdown by itself. ( n = 3 replicates per condition). Same box plot definitions as in Fig. . * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions. b p NPP ( p -nitrophenyl phosphate) assay of ΔPTPN1 PTP activity following addition of various amounts of Cu 1+ ( n = 12 replicates per condition). c Proteome profiler antibody array volcano plot depicting statistically significant increases in phosphorylation levels following HEK 293 T supplementation with 20 μM ZnCl 2 . ( n = 2 replicates for each conditio n ). d Changes in A549 EGR1 expression levels 60 min after ZnCl 2 supplementation. The fold-changes are overlayed on the fold-changes induced by CuCl 2 supplementation for reference. ( n = 2 replicates per condition). Same box plot definitions as in Fig. . e RNA-qPCR fold-changes of select transcripts 4 h post-supplementation of 500 nM CuGTSM or 5 µM <t>CS1</t> relative to DMSO treated A549 cells. ( n = 3 replicates per condition). Data points correspond to biological replicates, p -values calculated as paired two-tailed t-test. Same box plot definitions as in Fig. . Figure 4a, b, d, and e source data are provided as a Source Data file, as are exact p -values for Fig. 4a, e. * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions.
Cs1, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+cd2/CRACC%2FSLAMF7%2C+Human/pmc11322707-215-6-7
Average 92 stars, based on 1 article reviews
cs1 - by Bioz Stars, 2026-10
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R&D Systems recombinant proteins recombinant human cd2 fc chimera protein r d systems 1856 cd 050 mart 1 ela mutant epitope peptide
a Evaluation of the effects on EGR1 expression levels of 200 μM CuCl 2 (60 min treatment) following siRNA knockdown of various PTPs in A549 cells. Depicted are two interpretations of the results. ( top ) All fold-changes are reported relative to the negative control siRNA transfect (Neg.) without CuCl 2 supplementation. ( bottom ) Each result is reported as the fold-change between the denoted siRNA knockdown after 60 min 200 μM CuCl 2 supplementation and the siRNA knockdown by itself. ( n = 3 replicates per condition). Same box plot definitions as in Fig. . * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions. b p NPP ( p -nitrophenyl phosphate) assay of ΔPTPN1 PTP activity following addition of various amounts of Cu 1+ ( n = 12 replicates per condition). c Proteome profiler antibody array volcano plot depicting statistically significant increases in phosphorylation levels following HEK 293 T supplementation with 20 μM ZnCl 2 . ( n = 2 replicates for each conditio n ). d Changes in A549 EGR1 expression levels 60 min after ZnCl 2 supplementation. The fold-changes are overlayed on the fold-changes induced by CuCl 2 supplementation for reference. ( n = 2 replicates per condition). Same box plot definitions as in Fig. . e RNA-qPCR fold-changes of select transcripts 4 h post-supplementation of 500 nM CuGTSM or 5 µM <t>CS1</t> relative to DMSO treated A549 cells. ( n = 3 replicates per condition). Data points correspond to biological replicates, p -values calculated as paired two-tailed t-test. Same box plot definitions as in Fig. . Figure 4a, b, d, and e source data are provided as a Source Data file, as are exact p -values for Fig. 4a, e. * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions.
Recombinant Proteins Recombinant Human Cd2 Fc Chimera Protein R D Systems 1856 Cd 050 Mart 1 Ela Mutant Epitope Peptide, 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/product/human+cd2/Recombinant+Human+CD2+Fc+Chimera+Protein%2C+CF/pm37683639-193-116-124
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Elabscience Biotechnology anti cd2
a Evaluation of the effects on EGR1 expression levels of 200 μM CuCl 2 (60 min treatment) following siRNA knockdown of various PTPs in A549 cells. Depicted are two interpretations of the results. ( top ) All fold-changes are reported relative to the negative control siRNA transfect (Neg.) without CuCl 2 supplementation. ( bottom ) Each result is reported as the fold-change between the denoted siRNA knockdown after 60 min 200 μM CuCl 2 supplementation and the siRNA knockdown by itself. ( n = 3 replicates per condition). Same box plot definitions as in Fig. . * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions. b p NPP ( p -nitrophenyl phosphate) assay of ΔPTPN1 PTP activity following addition of various amounts of Cu 1+ ( n = 12 replicates per condition). c Proteome profiler antibody array volcano plot depicting statistically significant increases in phosphorylation levels following HEK 293 T supplementation with 20 μM ZnCl 2 . ( n = 2 replicates for each conditio n ). d Changes in A549 EGR1 expression levels 60 min after ZnCl 2 supplementation. The fold-changes are overlayed on the fold-changes induced by CuCl 2 supplementation for reference. ( n = 2 replicates per condition). Same box plot definitions as in Fig. . e RNA-qPCR fold-changes of select transcripts 4 h post-supplementation of 500 nM CuGTSM or 5 µM <t>CS1</t> relative to DMSO treated A549 cells. ( n = 3 replicates per condition). Data points correspond to biological replicates, p -values calculated as paired two-tailed t-test. Same box plot definitions as in Fig. . Figure 4a, b, d, and e source data are provided as a Source Data file, as are exact p -values for Fig. 4a, e. * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions.
Anti Cd2, supplied by Elabscience Biotechnology, 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/product/human+cd2/PE+Anti-Human+CD2+Antibody/10__1134_slash_s1068162025603787-166-24-54
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R&D Systems cd2 r d systems 1856 cd 050
a Evaluation of the effects on EGR1 expression levels of 200 μM CuCl 2 (60 min treatment) following siRNA knockdown of various PTPs in A549 cells. Depicted are two interpretations of the results. ( top ) All fold-changes are reported relative to the negative control siRNA transfect (Neg.) without CuCl 2 supplementation. ( bottom ) Each result is reported as the fold-change between the denoted siRNA knockdown after 60 min 200 μM CuCl 2 supplementation and the siRNA knockdown by itself. ( n = 3 replicates per condition). Same box plot definitions as in Fig. . * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions. b p NPP ( p -nitrophenyl phosphate) assay of ΔPTPN1 PTP activity following addition of various amounts of Cu 1+ ( n = 12 replicates per condition). c Proteome profiler antibody array volcano plot depicting statistically significant increases in phosphorylation levels following HEK 293 T supplementation with 20 μM ZnCl 2 . ( n = 2 replicates for each conditio n ). d Changes in A549 EGR1 expression levels 60 min after ZnCl 2 supplementation. The fold-changes are overlayed on the fold-changes induced by CuCl 2 supplementation for reference. ( n = 2 replicates per condition). Same box plot definitions as in Fig. . e RNA-qPCR fold-changes of select transcripts 4 h post-supplementation of 500 nM CuGTSM or 5 µM <t>CS1</t> relative to DMSO treated A549 cells. ( n = 3 replicates per condition). Data points correspond to biological replicates, p -values calculated as paired two-tailed t-test. Same box plot definitions as in Fig. . Figure 4a, b, d, and e source data are provided as a Source Data file, as are exact p -values for Fig. 4a, e. * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions.
Cd2 R D Systems 1856 Cd 050, 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/product/human+cd2/Recombinant+Human+CD2+Fc+Chimera+Protein%2C+CF/pm35338135-451-42-43
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Image Search Results


Figure 5. Virally induced constitutively active CD30 signaling results in more Cre-reporter+ cells within B cells. CAR//Cγ1-cre mice (dots) and LC30//Cγ1-cre mice (squares) were i.p. infected with MHV-68 hNGFR and splenic cells were analyzed 14 days post-infection. (A) Breeding scheme of LC30//Cγ1cre mice. The excision of the loxP-flanked stop cassette was followed by hCD2 reporter expression (Cre-reporter) and ligand-independent constitutively active CD30 signaling. (B) The splenic

Journal: Cells

Article Title: A Mouse Model to Study the Pathogenesis of γ-herpesviral Infections in Germinal Center B Cells.

doi: 10.3390/cells12242780

Figure Lengend Snippet: Figure 5. Virally induced constitutively active CD30 signaling results in more Cre-reporter+ cells within B cells. CAR//Cγ1-cre mice (dots) and LC30//Cγ1-cre mice (squares) were i.p. infected with MHV-68 hNGFR and splenic cells were analyzed 14 days post-infection. (A) Breeding scheme of LC30//Cγ1cre mice. The excision of the loxP-flanked stop cassette was followed by hCD2 reporter expression (Cre-reporter) and ligand-independent constitutively active CD30 signaling. (B) The splenic

Article Snippet: The CD19-PeVio770 (REA749), CD38-PeVio770 and human CD2 (hCD2)-PeVio770 (LT2) antibodies were all purchased from Miltenyi Biotech (Bergisch Gladbach, Germany).

Techniques: Infection, Expressing

(A–C) FILM acquisition of binder probes that recognize CD2, ICAM-1 (CD54) in the pSMAC, and CD45 in the dSMAC zones (10 nm pixels with 3-pixel Gaussian blurring). For CD2 and CD45, APC-conjugated antibodies were used; for ICAM-1, a nanobody Fab conjugated with Vio ® 667 was used. Cyan boxed region shows the IF image (103.17 nm pixels) corresponding to the white boxed region. (D–F) Zoom-in of the respective boxed regions for the panels to the left. Localizations are shown as peak-normalized 2D Gaussians with color-coded precision according to the colorbar. (G–I) Zoom-in of the respective boxed regions for the panels to the immediate left. Localizations are shown as crosses (indicating ±1-σ uncertainty in x and y ) with color-coded precision according to the colorbar.

Journal: bioRxiv

Article Title: Ångström Resolution with Flow Immunofluorescence Localization Microscopy (FILM)

doi: 10.64898/2025.12.16.694546

Figure Lengend Snippet: (A–C) FILM acquisition of binder probes that recognize CD2, ICAM-1 (CD54) in the pSMAC, and CD45 in the dSMAC zones (10 nm pixels with 3-pixel Gaussian blurring). For CD2 and CD45, APC-conjugated antibodies were used; for ICAM-1, a nanobody Fab conjugated with Vio ® 667 was used. Cyan boxed region shows the IF image (103.17 nm pixels) corresponding to the white boxed region. (D–F) Zoom-in of the respective boxed regions for the panels to the left. Localizations are shown as peak-normalized 2D Gaussians with color-coded precision according to the colorbar. (G–I) Zoom-in of the respective boxed regions for the panels to the immediate left. Localizations are shown as crosses (indicating ±1-σ uncertainty in x and y ) with color-coded precision according to the colorbar.

Article Snippet: α-tubulin (REA1136 REAfinityTM, h, APC, #130-119-541, Miltenyi Biotec), CD2 (REA972 REAfinityTM, h, APC, #130-116-150, Miltenyi Biotec), CD20 (REA780 REAfinityTM, h, APC, #130-111-339, Miltenyi Biotec), CD28 (REA612 REAfinityTM, h, APC, #130-118-343, Miltenyi Biotec), CD45 (REA1023 REAfinityTM, h/nhp, APC, #130-117-191, Miltenyi Biotec), CD54/ICAM-1 (REA266 REAfinityTM, h, APC, #130-120-711, Miltenyi Biotec), CD81 (REA513 REAfinityTM, h, APC, #130-119-787, Miltenyi Biotec), CD107a/LAMP1 (REA792 REAfinityTM, h, APC, #130-111-847, Miltenyi Biotec), IgD (REA740 REAfinityTM, h, APC, #130-110-644, Miltenyi Biotec), IgM (REAL689 REAdye_leaseTM, h, PE, #130-125-786, Miltenyi Biotec), Pan-Cytokeratin (REA1141 REAfinityTM, h, APC, #130-120-096, Miltenyi Biotec), β-catenin (REA480 REAfinityTM, h, APC, #130-124-444, Miltenyi Biotec), TCRα/β (REA652 REAfinityTM, h, APC, #130-113-535, Miltenyi Biotec), TOM22 (REA1185 REAfinityTM, APC, h/ms, #130-122-079, Miltenyi Biotec), DAPI Staining Solution (#130-111-570, Miltenyi Biotec), and ATTO 643 phalloidin (ATT-AD643-81, ATTO-TEC).

Techniques:

Expression of CD86 (M1) and CD206 (M2). (A) : Expression of CD86 (M1); (B) : Expression of CD206 (M2). # P < 0.05, ## P < 0.01 vs. sham; * p < 0.05, ** p < 0.01 vs. MCAO/R.

Journal: Frontiers in Pharmacology

Article Title: Exploration of the mechanism of Taohong Siwu Decoction for the treatment of ischemic stroke based on CCL2/CCR2 axis

doi: 10.3389/fphar.2024.1428572

Figure Lengend Snippet: Expression of CD86 (M1) and CD206 (M2). (A) : Expression of CD86 (M1); (B) : Expression of CD206 (M2). # P < 0.05, ## P < 0.01 vs. sham; * p < 0.05, ** p < 0.01 vs. MCAO/R.

Article Snippet: A11042), were both purchased from MultiSciences, APC anti-Human CD206 (LW1218) was purchased from Elabscience, human TNF-α (July 2023), Human matrix metalloproteinase 9 (MMP-9) (July 2023), human IL-6 (July 2023), human IL-4 (July 2023), rat TNF-α (May 2023), rat MMP-9 (May 2023), rat IL-6 (May 2023), rat IL-4 (May 2023) were purchased from Quanzhou Ruixin Biotechnology Co., Ltd., claudin-5 (cat.no.

Techniques: Expressing

Journal: Cell Reports Medicine

Article Title: SARS-CoV-2-Specific T Cells Exhibit Phenotypic Features of Helper Function, Lack of Terminal Differentiation, and High Proliferation Potential

doi: 10.1016/j.xcrm.2020.100081

Figure Lengend Snippet:

Article Snippet: CD2 , Fluidigm , Cat#3151003B.

Techniques: Purification, Recombinant, Electron Microscopy, Virus, Control, Clinical Proteomics, Staining, Antibody Labeling, Software

a Evaluation of the effects on EGR1 expression levels of 200 μM CuCl 2 (60 min treatment) following siRNA knockdown of various PTPs in A549 cells. Depicted are two interpretations of the results. ( top ) All fold-changes are reported relative to the negative control siRNA transfect (Neg.) without CuCl 2 supplementation. ( bottom ) Each result is reported as the fold-change between the denoted siRNA knockdown after 60 min 200 μM CuCl 2 supplementation and the siRNA knockdown by itself. ( n = 3 replicates per condition). Same box plot definitions as in Fig. . * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions. b p NPP ( p -nitrophenyl phosphate) assay of ΔPTPN1 PTP activity following addition of various amounts of Cu 1+ ( n = 12 replicates per condition). c Proteome profiler antibody array volcano plot depicting statistically significant increases in phosphorylation levels following HEK 293 T supplementation with 20 μM ZnCl 2 . ( n = 2 replicates for each conditio n ). d Changes in A549 EGR1 expression levels 60 min after ZnCl 2 supplementation. The fold-changes are overlayed on the fold-changes induced by CuCl 2 supplementation for reference. ( n = 2 replicates per condition). Same box plot definitions as in Fig. . e RNA-qPCR fold-changes of select transcripts 4 h post-supplementation of 500 nM CuGTSM or 5 µM CS1 relative to DMSO treated A549 cells. ( n = 3 replicates per condition). Data points correspond to biological replicates, p -values calculated as paired two-tailed t-test. Same box plot definitions as in Fig. . Figure 4a, b, d, and e source data are provided as a Source Data file, as are exact p -values for Fig. 4a, e. * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions.

Journal: Nature Communications

Article Title: PTPN2 copper-sensing relays copper level fluctuations into EGFR/CREB activation and associated CTR1 transcriptional repression

doi: 10.1038/s41467-024-50524-5

Figure Lengend Snippet: a Evaluation of the effects on EGR1 expression levels of 200 μM CuCl 2 (60 min treatment) following siRNA knockdown of various PTPs in A549 cells. Depicted are two interpretations of the results. ( top ) All fold-changes are reported relative to the negative control siRNA transfect (Neg.) without CuCl 2 supplementation. ( bottom ) Each result is reported as the fold-change between the denoted siRNA knockdown after 60 min 200 μM CuCl 2 supplementation and the siRNA knockdown by itself. ( n = 3 replicates per condition). Same box plot definitions as in Fig. . * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions. b p NPP ( p -nitrophenyl phosphate) assay of ΔPTPN1 PTP activity following addition of various amounts of Cu 1+ ( n = 12 replicates per condition). c Proteome profiler antibody array volcano plot depicting statistically significant increases in phosphorylation levels following HEK 293 T supplementation with 20 μM ZnCl 2 . ( n = 2 replicates for each conditio n ). d Changes in A549 EGR1 expression levels 60 min after ZnCl 2 supplementation. The fold-changes are overlayed on the fold-changes induced by CuCl 2 supplementation for reference. ( n = 2 replicates per condition). Same box plot definitions as in Fig. . e RNA-qPCR fold-changes of select transcripts 4 h post-supplementation of 500 nM CuGTSM or 5 µM CS1 relative to DMSO treated A549 cells. ( n = 3 replicates per condition). Data points correspond to biological replicates, p -values calculated as paired two-tailed t-test. Same box plot definitions as in Fig. . Figure 4a, b, d, and e source data are provided as a Source Data file, as are exact p -values for Fig. 4a, e. * denotes p < 0.05, ** denotes p < 0.01, and *** denotes p < 0.001 for two-sided t -test comparison between conditions.

Article Snippet: For Cu-GTSM (Cayman Chemical Company) and CS1 (MedChemExpress) treatments, the solid drugs were dissolved in DMSO to a final concentration of 1 mM.

Techniques: Expressing, Knockdown, Negative Control, Comparison, Activity Assay, Ab Array, Phospho-proteomics, Two Tailed Test