u2932 cells Search Results


90
Laboratory Animals Ltd hk2-knockdown u2932 cells
<t>HK2</t> was overexpressed in DLBCL cell lines. (a) HK2 expression in normal (Hmy2.CIR) and DLBCL (TMD8, OCI-Ly3, <t>U2932,</t> OCI-Ly1, OCI-Ly7, SU-DHL-4, and SU-DHL-6) cells were measured using qRT-PCR. (b–d) Protein expression levels of HK2, p-ERK1/2, and ERK1/2 were assessed using western blotting. The University of Alabama at Birmingham Cancer (UALCAN) data analysis portal was used to analyze (e) the expression levels of HK2 at individual cancer stages and (f) overall survival of patients with DLBCL. * P < 0.05 and ** P < 0.01 versus the Hmy2.CIR group. ▲ P < 0.05 Stage 1-versus-Stage 4 ( P -value: 2.502100 × 10 −2 ). ABC-DLBCL: activated B-cell-like (ABC) subtype of diffuse large B-cell lymphoma (DLBCL); GCB-DLBCL: Germinal center B-cell-like (GCB) subtype of diffuse large B-cell lymphoma (DLBCL).
Hk2 Knockdown U2932 Cells, supplied by Laboratory Animals Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/u2932+cells/pmc10579878-77-6-27?v=Laboratory+Animals+Ltd
Average 90 stars, based on 1 article reviews
hk2-knockdown u2932 cells - by Bioz Stars, 2026-07
90/100 stars
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90
iCell Bioscience Inc u2932 cells
<t>HK2</t> was overexpressed in DLBCL cell lines. (a) HK2 expression in normal (Hmy2.CIR) and DLBCL (TMD8, OCI-Ly3, <t>U2932,</t> OCI-Ly1, OCI-Ly7, SU-DHL-4, and SU-DHL-6) cells were measured using qRT-PCR. (b–d) Protein expression levels of HK2, p-ERK1/2, and ERK1/2 were assessed using western blotting. The University of Alabama at Birmingham Cancer (UALCAN) data analysis portal was used to analyze (e) the expression levels of HK2 at individual cancer stages and (f) overall survival of patients with DLBCL. * P < 0.05 and ** P < 0.01 versus the Hmy2.CIR group. ▲ P < 0.05 Stage 1-versus-Stage 4 ( P -value: 2.502100 × 10 −2 ). ABC-DLBCL: activated B-cell-like (ABC) subtype of diffuse large B-cell lymphoma (DLBCL); GCB-DLBCL: Germinal center B-cell-like (GCB) subtype of diffuse large B-cell lymphoma (DLBCL).
U2932 Cells, supplied by iCell Bioscience Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/u2932+cells/pm40099624-50-0-11?v=iCell+Bioscience+Inc
Average 90 stars, based on 1 article reviews
u2932 cells - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
BioVector Inc dlbcl cell lines (u2932, tmd8 and oci-ly3)
<t>HK2</t> was overexpressed in DLBCL cell lines. (a) HK2 expression in normal (Hmy2.CIR) and DLBCL (TMD8, OCI-Ly3, <t>U2932,</t> OCI-Ly1, OCI-Ly7, SU-DHL-4, and SU-DHL-6) cells were measured using qRT-PCR. (b–d) Protein expression levels of HK2, p-ERK1/2, and ERK1/2 were assessed using western blotting. The University of Alabama at Birmingham Cancer (UALCAN) data analysis portal was used to analyze (e) the expression levels of HK2 at individual cancer stages and (f) overall survival of patients with DLBCL. * P < 0.05 and ** P < 0.01 versus the Hmy2.CIR group. ▲ P < 0.05 Stage 1-versus-Stage 4 ( P -value: 2.502100 × 10 −2 ). ABC-DLBCL: activated B-cell-like (ABC) subtype of diffuse large B-cell lymphoma (DLBCL); GCB-DLBCL: Germinal center B-cell-like (GCB) subtype of diffuse large B-cell lymphoma (DLBCL).
Dlbcl Cell Lines (U2932, Tmd8 And Oci Ly3), supplied by BioVector Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/u2932+cells/pm33830472-37-0-16?v=BioVector+Inc
Average 90 stars, based on 1 article reviews
dlbcl cell lines (u2932, tmd8 and oci-ly3) - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier


Image Search Results


HK2 was overexpressed in DLBCL cell lines. (a) HK2 expression in normal (Hmy2.CIR) and DLBCL (TMD8, OCI-Ly3, U2932, OCI-Ly1, OCI-Ly7, SU-DHL-4, and SU-DHL-6) cells were measured using qRT-PCR. (b–d) Protein expression levels of HK2, p-ERK1/2, and ERK1/2 were assessed using western blotting. The University of Alabama at Birmingham Cancer (UALCAN) data analysis portal was used to analyze (e) the expression levels of HK2 at individual cancer stages and (f) overall survival of patients with DLBCL. * P < 0.05 and ** P < 0.01 versus the Hmy2.CIR group. ▲ P < 0.05 Stage 1-versus-Stage 4 ( P -value: 2.502100 × 10 −2 ). ABC-DLBCL: activated B-cell-like (ABC) subtype of diffuse large B-cell lymphoma (DLBCL); GCB-DLBCL: Germinal center B-cell-like (GCB) subtype of diffuse large B-cell lymphoma (DLBCL).

Journal: Open Life Sciences

Article Title: HK2 contributes to the proliferation, migration, and invasion of diffuse large B-cell lymphoma cells by enhancing the ERK1/2 signaling pathway

doi: 10.1515/biol-2022-0726

Figure Lengend Snippet: HK2 was overexpressed in DLBCL cell lines. (a) HK2 expression in normal (Hmy2.CIR) and DLBCL (TMD8, OCI-Ly3, U2932, OCI-Ly1, OCI-Ly7, SU-DHL-4, and SU-DHL-6) cells were measured using qRT-PCR. (b–d) Protein expression levels of HK2, p-ERK1/2, and ERK1/2 were assessed using western blotting. The University of Alabama at Birmingham Cancer (UALCAN) data analysis portal was used to analyze (e) the expression levels of HK2 at individual cancer stages and (f) overall survival of patients with DLBCL. * P < 0.05 and ** P < 0.01 versus the Hmy2.CIR group. ▲ P < 0.05 Stage 1-versus-Stage 4 ( P -value: 2.502100 × 10 −2 ). ABC-DLBCL: activated B-cell-like (ABC) subtype of diffuse large B-cell lymphoma (DLBCL); GCB-DLBCL: Germinal center B-cell-like (GCB) subtype of diffuse large B-cell lymphoma (DLBCL).

Article Snippet: In brief, 5 × 10 6 HK2-knockdown U2932 cells and the corresponding control cells were subcutaneously injected into the flanks of 4-week-old BALB/c nude mice (Shanghai SLAC Laboratory Animals Ltd., China).

Techniques: Expressing, Quantitative RT-PCR, Western Blot

HK2 knockdown inhibits U2932 and SU-DHL-4 cell proliferation in vitro . (a) HK2 was knocked down in U2932 and SU-DHL-4 cells using siRNAs. (b) The viability of HK2-silenced and FR180204-treated (5 μM) U2932 and SU-DHL-4 cells was assessed using the CCK-8 assays. (c) Colony formation assays were used to assess the clone numbers of HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. * P < 0.05 and ** P < 0.01 versus the si-NC group.

Journal: Open Life Sciences

Article Title: HK2 contributes to the proliferation, migration, and invasion of diffuse large B-cell lymphoma cells by enhancing the ERK1/2 signaling pathway

doi: 10.1515/biol-2022-0726

Figure Lengend Snippet: HK2 knockdown inhibits U2932 and SU-DHL-4 cell proliferation in vitro . (a) HK2 was knocked down in U2932 and SU-DHL-4 cells using siRNAs. (b) The viability of HK2-silenced and FR180204-treated (5 μM) U2932 and SU-DHL-4 cells was assessed using the CCK-8 assays. (c) Colony formation assays were used to assess the clone numbers of HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. * P < 0.05 and ** P < 0.01 versus the si-NC group.

Article Snippet: In brief, 5 × 10 6 HK2-knockdown U2932 cells and the corresponding control cells were subcutaneously injected into the flanks of 4-week-old BALB/c nude mice (Shanghai SLAC Laboratory Animals Ltd., China).

Techniques: In Vitro, CCK-8 Assay

HK2 knockdown inhibits U2932 and SU-DHL-4 cell migration and invasion in vitro . (a) Transwell assays were used to analyze the effects of HK2 knockdown on the migration and invasion of U2932 and SU-DHL-4 cells. (b) Western blotting was used to assess the expression levels of E-cadherin and N-cadherin in HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. * P < 0.05 and ** P < 0.01 versus the si-NC group.

Journal: Open Life Sciences

Article Title: HK2 contributes to the proliferation, migration, and invasion of diffuse large B-cell lymphoma cells by enhancing the ERK1/2 signaling pathway

doi: 10.1515/biol-2022-0726

Figure Lengend Snippet: HK2 knockdown inhibits U2932 and SU-DHL-4 cell migration and invasion in vitro . (a) Transwell assays were used to analyze the effects of HK2 knockdown on the migration and invasion of U2932 and SU-DHL-4 cells. (b) Western blotting was used to assess the expression levels of E-cadherin and N-cadherin in HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. * P < 0.05 and ** P < 0.01 versus the si-NC group.

Article Snippet: In brief, 5 × 10 6 HK2-knockdown U2932 cells and the corresponding control cells were subcutaneously injected into the flanks of 4-week-old BALB/c nude mice (Shanghai SLAC Laboratory Animals Ltd., China).

Techniques: Migration, In Vitro, Western Blot, Expressing

HK2 knockdown promotes U2932 and SU-DHL-4 cell apoptosis in vitro . (a) Flow cytometry assay was employed to measure U2932 and SU-DHL-4 cell apoptosis. (b) Representative blots and statistical analysis of Bax, Bcl-2, caspase-3, ERK1/2, and p-ERK1/2 in HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. (c) Representative blots and statistical analysis of HIF-1α and Ki67 in HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. * P < 0.05 and ** P < 0.01 versus the si-NC group.

Journal: Open Life Sciences

Article Title: HK2 contributes to the proliferation, migration, and invasion of diffuse large B-cell lymphoma cells by enhancing the ERK1/2 signaling pathway

doi: 10.1515/biol-2022-0726

Figure Lengend Snippet: HK2 knockdown promotes U2932 and SU-DHL-4 cell apoptosis in vitro . (a) Flow cytometry assay was employed to measure U2932 and SU-DHL-4 cell apoptosis. (b) Representative blots and statistical analysis of Bax, Bcl-2, caspase-3, ERK1/2, and p-ERK1/2 in HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. (c) Representative blots and statistical analysis of HIF-1α and Ki67 in HK2-silenced and FR180204-treated U2932 and SU-DHL-4 cells. * P < 0.05 and ** P < 0.01 versus the si-NC group.

Article Snippet: In brief, 5 × 10 6 HK2-knockdown U2932 cells and the corresponding control cells were subcutaneously injected into the flanks of 4-week-old BALB/c nude mice (Shanghai SLAC Laboratory Animals Ltd., China).

Techniques: In Vitro, Flow Cytometry