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DSMZ supm2
Supm2, supplied by DSMZ, used in various techniques. Bioz Stars score: 94/100, based on 66 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/supm2/product/DSMZ
Average 94 stars, based on 66 article reviews
supm2 - by Bioz Stars, 2026-04
94/100 stars

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supm2  (DSMZ)
94
DSMZ supm2
Supm2, supplied by DSMZ, 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/supm2/product/DSMZ
Average 94 stars, based on 1 article reviews
supm2 - by Bioz Stars, 2026-04
94/100 stars
  Buy from Supplier

95
DSMZ su dhl 1 supm2
(A) Volcano plot and (B) MA plot of circular RNA expression comparing ALK(+) ALCL primary biopsies (n=39) and healthy tissues (reactive lymph nodes, RLN, n=9). (C) expression of circZBTB46 (left) and ZBTB46 mRNA (right) assessed by RNA-Seq in ALK(+) ALCL primary samples versus RLN. (D) ZBTB46 mRNA expression (RMA) from microarray datasets in ALK(+) ALCL (n=61), angioimmunoblastic T-cell lymphoma (AITL, n=83) and peripheral T-cell lymphoma not otherwise specified (PTCL-NOS, n=71) primary biopsies. (E) ZBTB46 mRNA expression (log2 of the transcript count per million (lenghScaled TPM) from RNA-Seq data in five ALK(+) ALCL cell lines (KARPAS-299, <t>SU-DHL-1,</t> SUP-M2, Pio, COST), two ALK(-) ALCL cell lines (FEPD, MAC-2A) and CD3(+) lymphocytes stimulated (S, n=3) or not (NS, n=3). (F) Quantitative real-time PCR (RTLqPCR) analysis of circZBTB46 and ZBTB46 mRNAs in the same cell types. MLN51 was used as an internal control. Values are expressed as 2^(–Δ)Ct relative ratios. Experiments were performed at least in triplicate. Statistical significance was assessed via an unpaired two-tailed Student’s t test with Welch’s correction: P < 0.01 ( ** ), P < 0.001 (*** ), P < 0.0001 (**** ), ns = not significant. Data are expressed as means ± SD. (G) ZBTB46 mRNA expression across hematological malignancies in the Cancer Cell Line Encyclopedia (CCLE) dataset. (H) Representative immunohistochemical image of an ALK(+) ALCL primary tumor showing ZBTB46 (brown, arrowhead) and CD68 (red, arrow) expression. Cell nuclei were counterstained with hematoxylin (blue). Original magnification, ×24.6.
Su Dhl 1 Supm2, supplied by DSMZ, 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/su dhl 1 supm2/product/DSMZ
Average 95 stars, based on 1 article reviews
su dhl 1 supm2 - by Bioz Stars, 2026-04
95/100 stars
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94
DSMZ supm2 l82 dhl1 tlbr1
(A) Volcano plot and (B) MA plot of circular RNA expression comparing ALK(+) ALCL primary biopsies (n=39) and healthy tissues (reactive lymph nodes, RLN, n=9). (C) expression of circZBTB46 (left) and ZBTB46 mRNA (right) assessed by RNA-Seq in ALK(+) ALCL primary samples versus RLN. (D) ZBTB46 mRNA expression (RMA) from microarray datasets in ALK(+) ALCL (n=61), angioimmunoblastic T-cell lymphoma (AITL, n=83) and peripheral T-cell lymphoma not otherwise specified (PTCL-NOS, n=71) primary biopsies. (E) ZBTB46 mRNA expression (log2 of the transcript count per million (lenghScaled TPM) from RNA-Seq data in five ALK(+) ALCL cell lines (KARPAS-299, <t>SU-DHL-1,</t> SUP-M2, Pio, COST), two ALK(-) ALCL cell lines (FEPD, MAC-2A) and CD3(+) lymphocytes stimulated (S, n=3) or not (NS, n=3). (F) Quantitative real-time PCR (RTLqPCR) analysis of circZBTB46 and ZBTB46 mRNAs in the same cell types. MLN51 was used as an internal control. Values are expressed as 2^(–Δ)Ct relative ratios. Experiments were performed at least in triplicate. Statistical significance was assessed via an unpaired two-tailed Student’s t test with Welch’s correction: P < 0.01 ( ** ), P < 0.001 (*** ), P < 0.0001 (**** ), ns = not significant. Data are expressed as means ± SD. (G) ZBTB46 mRNA expression across hematological malignancies in the Cancer Cell Line Encyclopedia (CCLE) dataset. (H) Representative immunohistochemical image of an ALK(+) ALCL primary tumor showing ZBTB46 (brown, arrowhead) and CD68 (red, arrow) expression. Cell nuclei were counterstained with hematoxylin (blue). Original magnification, ×24.6.
Supm2 L82 Dhl1 Tlbr1, supplied by DSMZ, 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/supm2 l82 dhl1 tlbr1/product/DSMZ
Average 94 stars, based on 1 article reviews
supm2 l82 dhl1 tlbr1 - by Bioz Stars, 2026-04
94/100 stars
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94
DSMZ supm2 cell line

Supm2 Cell Line, supplied by DSMZ, 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/supm2 cell line/product/DSMZ
Average 94 stars, based on 1 article reviews
supm2 cell line - by Bioz Stars, 2026-04
94/100 stars
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DSMZ supm2 dsmz cat

Supm2 Dsmz Cat, supplied by DSMZ, 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/supm2 dsmz cat/product/DSMZ
Average 94 stars, based on 1 article reviews
supm2 dsmz cat - by Bioz Stars, 2026-04
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DSMZ alk + alcl cell lines supm2 and uconn-l2

Alk + Alcl Cell Lines Supm2 And Uconn L2, supplied by DSMZ, 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/result/alk + alcl cell lines supm2 and uconn-l2/product/DSMZ
Average 90 stars, based on 1 article reviews
alk + alcl cell lines supm2 and uconn-l2 - by Bioz Stars, 2026-04
90/100 stars
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(A) Volcano plot and (B) MA plot of circular RNA expression comparing ALK(+) ALCL primary biopsies (n=39) and healthy tissues (reactive lymph nodes, RLN, n=9). (C) expression of circZBTB46 (left) and ZBTB46 mRNA (right) assessed by RNA-Seq in ALK(+) ALCL primary samples versus RLN. (D) ZBTB46 mRNA expression (RMA) from microarray datasets in ALK(+) ALCL (n=61), angioimmunoblastic T-cell lymphoma (AITL, n=83) and peripheral T-cell lymphoma not otherwise specified (PTCL-NOS, n=71) primary biopsies. (E) ZBTB46 mRNA expression (log2 of the transcript count per million (lenghScaled TPM) from RNA-Seq data in five ALK(+) ALCL cell lines (KARPAS-299, SU-DHL-1, SUP-M2, Pio, COST), two ALK(-) ALCL cell lines (FEPD, MAC-2A) and CD3(+) lymphocytes stimulated (S, n=3) or not (NS, n=3). (F) Quantitative real-time PCR (RTLqPCR) analysis of circZBTB46 and ZBTB46 mRNAs in the same cell types. MLN51 was used as an internal control. Values are expressed as 2^(–Δ)Ct relative ratios. Experiments were performed at least in triplicate. Statistical significance was assessed via an unpaired two-tailed Student’s t test with Welch’s correction: P < 0.01 ( ** ), P < 0.001 (*** ), P < 0.0001 (**** ), ns = not significant. Data are expressed as means ± SD. (G) ZBTB46 mRNA expression across hematological malignancies in the Cancer Cell Line Encyclopedia (CCLE) dataset. (H) Representative immunohistochemical image of an ALK(+) ALCL primary tumor showing ZBTB46 (brown, arrowhead) and CD68 (red, arrow) expression. Cell nuclei were counterstained with hematoxylin (blue). Original magnification, ×24.6.

Journal: bioRxiv

Article Title: CircZBTB46, a promising therapeutic target in crizotinib resistant ALK-positive T lymphomas

doi: 10.64898/2026.01.13.699235

Figure Lengend Snippet: (A) Volcano plot and (B) MA plot of circular RNA expression comparing ALK(+) ALCL primary biopsies (n=39) and healthy tissues (reactive lymph nodes, RLN, n=9). (C) expression of circZBTB46 (left) and ZBTB46 mRNA (right) assessed by RNA-Seq in ALK(+) ALCL primary samples versus RLN. (D) ZBTB46 mRNA expression (RMA) from microarray datasets in ALK(+) ALCL (n=61), angioimmunoblastic T-cell lymphoma (AITL, n=83) and peripheral T-cell lymphoma not otherwise specified (PTCL-NOS, n=71) primary biopsies. (E) ZBTB46 mRNA expression (log2 of the transcript count per million (lenghScaled TPM) from RNA-Seq data in five ALK(+) ALCL cell lines (KARPAS-299, SU-DHL-1, SUP-M2, Pio, COST), two ALK(-) ALCL cell lines (FEPD, MAC-2A) and CD3(+) lymphocytes stimulated (S, n=3) or not (NS, n=3). (F) Quantitative real-time PCR (RTLqPCR) analysis of circZBTB46 and ZBTB46 mRNAs in the same cell types. MLN51 was used as an internal control. Values are expressed as 2^(–Δ)Ct relative ratios. Experiments were performed at least in triplicate. Statistical significance was assessed via an unpaired two-tailed Student’s t test with Welch’s correction: P < 0.01 ( ** ), P < 0.001 (*** ), P < 0.0001 (**** ), ns = not significant. Data are expressed as means ± SD. (G) ZBTB46 mRNA expression across hematological malignancies in the Cancer Cell Line Encyclopedia (CCLE) dataset. (H) Representative immunohistochemical image of an ALK(+) ALCL primary tumor showing ZBTB46 (brown, arrowhead) and CD68 (red, arrow) expression. Cell nuclei were counterstained with hematoxylin (blue). Original magnification, ×24.6.

Article Snippet: The ALCL cell lines KARPAS-299, SU-DHL-1 SUPM2, Pio and COST, which carry the t(2;5)(p23;q35) translocation, were obtained from the DSMZ (German Collection of Microorganisms and Cell Culture, Leibnitz, Germany) or established locally .

Techniques: RNA Expression, Expressing, RNA Sequencing, Microarray, Real-time Polymerase Chain Reaction, Control, Two Tailed Test, Immunohistochemical staining

(A) Relative expression of circZBTB46 and ZBTB46 mRNAs in COST and KARPAS-299 cells transfected for 48 h with control siRNA (siCTL) or two different circZBTB46-targeting siRNAs (siCircZBTB46#1 and #2), as measured by RTLqPCR. (B) Viability (Annexin V-Pacific Blue/PI flow cytometry) of COST and KARPAS-299 cells transfected with siCircZBTB46#1 or #2 and subsequently treated with crizotinib (3 µM, 48 h). (C) Relative expression of circZBTB46 and ZBTB46 mRNAs in COST, SUPM2 and Pio cells transduced with Cas13 and either control gRNA (CTL) or gRNA targeting circZBTB46, as assessed by RTLqPCR. (D) Viability (Annexin V-Pacific Blue/PI flow cytometry) of COST, SUPM2 and Pio cells transduced as described in (C) and treated with crizotinib (100 or 200 nM) for 7 days. ( E ) Relative expression of circZBTB46 and ZBTB46 mRNAs in crizotinib-resistant cells established from MTK PDX-derived cells transfected for 48 h with control siRNA (siCTL) or two different siRNAs targeting circZBTB46 (siCircZBTB46#1 and #2), as measured by RTLqPCR. ( F-G ) Cell viability assessed by Annexin V-Pacific Blue/PI staining (flow cytometry) in crizotinib-resistant cells established from MTK PDX-derived cells transfected with siCircZBTB46#1 or #2, without treatment ( F ) or after crizotinib exposure ( G ) (400 nM, 48 h). ( H ) Relative expression of circZBTB46 and ZBTB46 mRNAs in COST crizotinib-resistant cells (COSTR200) after lentiviral transduction with circZBTB46-targeting shRNAs, as measured by RTLqPCR. ( I ) Viability of COSTR200 cells determined by Annexin V/PI staining (flow cytometry) after transduction with circZBTB46 shRNA and subsequent treatment with crizotinib (1,000 nM, 7 days). MLN51 was used as an internal control for RTLqPCR. Expression data are displayed as 2-ΔΔCt relative values. Statistical significance was assessed via an unpaired two-tailed Student t test with Welch correction: P < 0.05 ( * ), P < 0.01 (** ), P < 0.0001 ( **** ), ns = not significant. Data are expressed as means ± SEMs.

Journal: bioRxiv

Article Title: CircZBTB46, a promising therapeutic target in crizotinib resistant ALK-positive T lymphomas

doi: 10.64898/2026.01.13.699235

Figure Lengend Snippet: (A) Relative expression of circZBTB46 and ZBTB46 mRNAs in COST and KARPAS-299 cells transfected for 48 h with control siRNA (siCTL) or two different circZBTB46-targeting siRNAs (siCircZBTB46#1 and #2), as measured by RTLqPCR. (B) Viability (Annexin V-Pacific Blue/PI flow cytometry) of COST and KARPAS-299 cells transfected with siCircZBTB46#1 or #2 and subsequently treated with crizotinib (3 µM, 48 h). (C) Relative expression of circZBTB46 and ZBTB46 mRNAs in COST, SUPM2 and Pio cells transduced with Cas13 and either control gRNA (CTL) or gRNA targeting circZBTB46, as assessed by RTLqPCR. (D) Viability (Annexin V-Pacific Blue/PI flow cytometry) of COST, SUPM2 and Pio cells transduced as described in (C) and treated with crizotinib (100 or 200 nM) for 7 days. ( E ) Relative expression of circZBTB46 and ZBTB46 mRNAs in crizotinib-resistant cells established from MTK PDX-derived cells transfected for 48 h with control siRNA (siCTL) or two different siRNAs targeting circZBTB46 (siCircZBTB46#1 and #2), as measured by RTLqPCR. ( F-G ) Cell viability assessed by Annexin V-Pacific Blue/PI staining (flow cytometry) in crizotinib-resistant cells established from MTK PDX-derived cells transfected with siCircZBTB46#1 or #2, without treatment ( F ) or after crizotinib exposure ( G ) (400 nM, 48 h). ( H ) Relative expression of circZBTB46 and ZBTB46 mRNAs in COST crizotinib-resistant cells (COSTR200) after lentiviral transduction with circZBTB46-targeting shRNAs, as measured by RTLqPCR. ( I ) Viability of COSTR200 cells determined by Annexin V/PI staining (flow cytometry) after transduction with circZBTB46 shRNA and subsequent treatment with crizotinib (1,000 nM, 7 days). MLN51 was used as an internal control for RTLqPCR. Expression data are displayed as 2-ΔΔCt relative values. Statistical significance was assessed via an unpaired two-tailed Student t test with Welch correction: P < 0.05 ( * ), P < 0.01 (** ), P < 0.0001 ( **** ), ns = not significant. Data are expressed as means ± SEMs.

Article Snippet: The ALCL cell lines KARPAS-299, SU-DHL-1 SUPM2, Pio and COST, which carry the t(2;5)(p23;q35) translocation, were obtained from the DSMZ (German Collection of Microorganisms and Cell Culture, Leibnitz, Germany) or established locally .

Techniques: Expressing, Transfection, Control, Flow Cytometry, Transduction, Derivative Assay, Staining, shRNA, Two Tailed Test

Journal: Cell Reports Medicine

Article Title: A patient-derived T cell lymphoma biorepository uncovers pathogenetic mechanisms and host-related therapeutic vulnerabilities

doi: 10.1016/j.xcrm.2025.102029

Figure Lengend Snippet:

Article Snippet: SUPM2 cell line , DSMZ , ACC 509.

Techniques: Transduction, Recombinant, Saline, Software, Sterility, Transferring, Ointment