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bjab cell ccl22 induction assay innate immune activation potential  (DSMZ)


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    DSMZ bjab cell ccl22 induction assay innate immune activation potential
    Bjab Cell Ccl22 Induction Assay Innate Immune Activation Potential, supplied by DSMZ, used in various techniques. Bioz Stars score: 95/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bjab+cells/BJAB/pm42856037-77-0-18
    Average 95 stars, based on 80 article reviews
    bjab cell ccl22 induction assay innate immune activation potential - by Bioz Stars, 2026-11
    95/100 stars

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    Cell Culture:

    Article Title: Linkage modified oligomeric compounds and uses thereof
    Article Snippet: .. Immortalized human Burkitt lymphoma B cells, BJAB cells (DSMZ, Cat #ACC 757), were cultured in RPMI1640 medium containing 20% fetal bovine serum at 37° C. and 5% CO2. ..

    Article Title: The conformation of tetraspanins CD53 and CD81 differentially affects their nanoscale organization and interaction with their partners
    Article Snippet: .. BJAB cells (DSMZ, cat: ACC757, mycoplasma-negative) were cultured at 37 °C and 5% CO 2 in RPMI-1640 + 10% fetal bovine serum + 1% antibiotics/antimycotics (AA) + 1% ultraglutamine. .. Transfection of 5 × 10 6 cells with 2 μg plasmid was performed with the SF Cell Line 4D-Nucleofector X Kit L (Lonza) and the AMAXA Nucleofector biosystem (Program DS104).

    Infection:

    Article Title: Endothelial cells infected with Kaposi’s sarcoma-associated herpesvirus display distinct viscoelasticity and morphology
    Article Snippet: .. BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 cells, expresses the green fluorescent protein (GFP) and the red fluorescent protein (RFP) driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker., HuARLT2 cells are a conditionally-immortalised human umbilical vein endothelial cell line (HUVEC) derivative established via the expression of doxycycline-inducible transgenes simian virus 40 (SV40) large T antigen (TAg) and human telomerase reverse transcriptase (hTert). .. LECs are a telomerase-immortalised human lymphatic endothelial cell (LEC) line., Both HuARLT2 and LEC cell lines are well-established models for investigating KS mechanisms in vitro ., HEK-293T (DSMZ No.: ACC 305) cells are derived from human embryonic kidney 293 cells (HEK-293, Cellonex, C293-C) by stably expressing the transgenes SV40 and Tag.

    Article Title: Endothelial Cells Stably Infected with Recombinant Kaposi’s Sarcoma-Associated Herpesvirus Display Distinct Viscoelastic and Morphological Properties
    Article Snippet: High-level illustration of sequential steps (1–6) of the approach used. (Created with BioRender.com) .. As previously described [ ], BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 primary effusion lymphoma cells, expresses the green fluorescent protein (GFP) to indicate latency and the red fluorescent protein (RFP) to indicate lytic infection driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker [ , ]. ..

    Recombinant:

    Article Title: Endothelial cells infected with Kaposi’s sarcoma-associated herpesvirus display distinct viscoelasticity and morphology
    Article Snippet: .. BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 cells, expresses the green fluorescent protein (GFP) and the red fluorescent protein (RFP) driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker., HuARLT2 cells are a conditionally-immortalised human umbilical vein endothelial cell line (HUVEC) derivative established via the expression of doxycycline-inducible transgenes simian virus 40 (SV40) large T antigen (TAg) and human telomerase reverse transcriptase (hTert). .. LECs are a telomerase-immortalised human lymphatic endothelial cell (LEC) line., Both HuARLT2 and LEC cell lines are well-established models for investigating KS mechanisms in vitro ., HEK-293T (DSMZ No.: ACC 305) cells are derived from human embryonic kidney 293 cells (HEK-293, Cellonex, C293-C) by stably expressing the transgenes SV40 and Tag.

    Article Title: Endothelial Cells Stably Infected with Recombinant Kaposi’s Sarcoma-Associated Herpesvirus Display Distinct Viscoelastic and Morphological Properties
    Article Snippet: High-level illustration of sequential steps (1–6) of the approach used. (Created with BioRender.com) .. As previously described [ ], BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 primary effusion lymphoma cells, expresses the green fluorescent protein (GFP) to indicate latency and the red fluorescent protein (RFP) to indicate lytic infection driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker [ , ]. ..

    Isolation:

    Article Title: Endothelial cells infected with Kaposi’s sarcoma-associated herpesvirus display distinct viscoelasticity and morphology
    Article Snippet: .. BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 cells, expresses the green fluorescent protein (GFP) and the red fluorescent protein (RFP) driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker., HuARLT2 cells are a conditionally-immortalised human umbilical vein endothelial cell line (HUVEC) derivative established via the expression of doxycycline-inducible transgenes simian virus 40 (SV40) large T antigen (TAg) and human telomerase reverse transcriptase (hTert). .. LECs are a telomerase-immortalised human lymphatic endothelial cell (LEC) line., Both HuARLT2 and LEC cell lines are well-established models for investigating KS mechanisms in vitro ., HEK-293T (DSMZ No.: ACC 305) cells are derived from human embryonic kidney 293 cells (HEK-293, Cellonex, C293-C) by stably expressing the transgenes SV40 and Tag.

    Article Title: Endothelial Cells Stably Infected with Recombinant Kaposi’s Sarcoma-Associated Herpesvirus Display Distinct Viscoelastic and Morphological Properties
    Article Snippet: High-level illustration of sequential steps (1–6) of the approach used. (Created with BioRender.com) .. As previously described [ ], BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 primary effusion lymphoma cells, expresses the green fluorescent protein (GFP) to indicate latency and the red fluorescent protein (RFP) to indicate lytic infection driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker [ , ]. ..

    Marker:

    Article Title: Endothelial cells infected with Kaposi’s sarcoma-associated herpesvirus display distinct viscoelasticity and morphology
    Article Snippet: .. BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 cells, expresses the green fluorescent protein (GFP) and the red fluorescent protein (RFP) driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker., HuARLT2 cells are a conditionally-immortalised human umbilical vein endothelial cell line (HUVEC) derivative established via the expression of doxycycline-inducible transgenes simian virus 40 (SV40) large T antigen (TAg) and human telomerase reverse transcriptase (hTert). .. LECs are a telomerase-immortalised human lymphatic endothelial cell (LEC) line., Both HuARLT2 and LEC cell lines are well-established models for investigating KS mechanisms in vitro ., HEK-293T (DSMZ No.: ACC 305) cells are derived from human embryonic kidney 293 cells (HEK-293, Cellonex, C293-C) by stably expressing the transgenes SV40 and Tag.

    Article Title: Endothelial Cells Stably Infected with Recombinant Kaposi’s Sarcoma-Associated Herpesvirus Display Distinct Viscoelastic and Morphological Properties
    Article Snippet: High-level illustration of sequential steps (1–6) of the approach used. (Created with BioRender.com) .. As previously described [ ], BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 primary effusion lymphoma cells, expresses the green fluorescent protein (GFP) to indicate latency and the red fluorescent protein (RFP) to indicate lytic infection driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker [ , ]. ..

    Expressing:

    Article Title: Endothelial cells infected with Kaposi’s sarcoma-associated herpesvirus display distinct viscoelasticity and morphology
    Article Snippet: .. BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 cells, expresses the green fluorescent protein (GFP) and the red fluorescent protein (RFP) driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker., HuARLT2 cells are a conditionally-immortalised human umbilical vein endothelial cell line (HUVEC) derivative established via the expression of doxycycline-inducible transgenes simian virus 40 (SV40) large T antigen (TAg) and human telomerase reverse transcriptase (hTert). .. LECs are a telomerase-immortalised human lymphatic endothelial cell (LEC) line., Both HuARLT2 and LEC cell lines are well-established models for investigating KS mechanisms in vitro ., HEK-293T (DSMZ No.: ACC 305) cells are derived from human embryonic kidney 293 cells (HEK-293, Cellonex, C293-C) by stably expressing the transgenes SV40 and Tag.

    Virus:

    Article Title: Endothelial cells infected with Kaposi’s sarcoma-associated herpesvirus display distinct viscoelasticity and morphology
    Article Snippet: .. BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 cells, expresses the green fluorescent protein (GFP) and the red fluorescent protein (RFP) driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker., HuARLT2 cells are a conditionally-immortalised human umbilical vein endothelial cell line (HUVEC) derivative established via the expression of doxycycline-inducible transgenes simian virus 40 (SV40) large T antigen (TAg) and human telomerase reverse transcriptase (hTert). .. LECs are a telomerase-immortalised human lymphatic endothelial cell (LEC) line., Both HuARLT2 and LEC cell lines are well-established models for investigating KS mechanisms in vitro ., HEK-293T (DSMZ No.: ACC 305) cells are derived from human embryonic kidney 293 cells (HEK-293, Cellonex, C293-C) by stably expressing the transgenes SV40 and Tag.

    Reverse Transcription:

    Article Title: Endothelial cells infected with Kaposi’s sarcoma-associated herpesvirus display distinct viscoelasticity and morphology
    Article Snippet: .. BJAB-rKSHV.219 were established from BJAB cells (DSMZ No.: ACC 757), a human Burkitt lymphoma-derived cell line, via stable infection with a recombinant Kaposi’s sarcoma-associated herpesvirus (rKSHV.219). rKSHV.219, isolated from JSC-1 cells, expresses the green fluorescent protein (GFP) and the red fluorescent protein (RFP) driven by cellular EF-1α and KSHV lytic PAN promoters, respectively, and contains a gene for puromycin resistance as a selectable marker., HuARLT2 cells are a conditionally-immortalised human umbilical vein endothelial cell line (HUVEC) derivative established via the expression of doxycycline-inducible transgenes simian virus 40 (SV40) large T antigen (TAg) and human telomerase reverse transcriptase (hTert). .. LECs are a telomerase-immortalised human lymphatic endothelial cell (LEC) line., Both HuARLT2 and LEC cell lines are well-established models for investigating KS mechanisms in vitro ., HEK-293T (DSMZ No.: ACC 305) cells are derived from human embryonic kidney 293 cells (HEK-293, Cellonex, C293-C) by stably expressing the transgenes SV40 and Tag.



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    DSMZ bjab b cell lymphoma lines
    Activated DDR1 downregulates expression of the mitotic kinesin, CENPE . (A) Upper panels show the significant overlap between genes upregulated by DDR1 in normal GC B cells and those upregulated in either GCB‐ or ABC‐DLBCL compared with normal GC B cells (total genes on both platforms = 26,438). The lower panel shows GO analysis of genes upregulated by DDR1 in normal GC B cells and also upregulated in both GCB and ABC‐DLBCL. Open bars indicate the percentage of genes present in the GO term that would be expected to be observed in the regulated gene list by chance. Shaded bars indicate the percentage of genes in the regulated list with a given GO term that were actually observed. (B) RT‐qPCR confirming that collagen treatment of DDR1‐expressing GC B cells significantly reduced the mRNA levels of CENPE . Shown are triplicate data on tonsillar GC B cells isolated from three different donors (T20, T21 and T42). (C) Compared to empty vector (EV) control, the addition of collagen significantly reduced CENPE mRNA expression in DDR1‐expressing B‐cell lines, <t>BJAB</t> (maximally after 6 h of stimulation) and DG75 (maximally after 2 h of stimulation). Data are representative of three separate biological replicates. (D) Activation of an ectopically expressed DDR1 reduced CENPE protein expression in both BJAB and DG75 cells. An antibody specific for DDR1 phosphorylated on Tyr792 was used to confirm activation of DDR1. As expected, the activation of DDR1 also reduced total DDR1 levels. β‐Actin was used as a loading control. Data shown are representative of three separate biological replicates. (E) A constitutively activated DDR1 construct also downregulated CENPE protein expression. Shown here are the mean fluorescence intensities for DDR1 and CENPE in DG75 cells transfected with the constitutively active DDR1 gene. Cells expressing DDR1 were significantly more likely to lack CENPE protein expression than were untransfected cells in the same population ( p < 0.0001). (F) Immunohistochemistry showing the downregulation of CENPE protein in DLBCL tumour cells. Top left panel shows strong expression of CENPE protein in a normal germinal centre (GC) of tonsil. Original magnification ×200. Remaining panels show examples of staining in a case in which CENPE was not detected in tumour cells (top right), a case with weak expression in tumour cells (bottom left) and a case showing strong staining (bottom right). Original magnification ×400. Black arrows show tumour cells. Red arrows indicate nonmalignant cells that are positive for CENPE.
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    Image Search Results


    Activated DDR1 downregulates expression of the mitotic kinesin, CENPE . (A) Upper panels show the significant overlap between genes upregulated by DDR1 in normal GC B cells and those upregulated in either GCB‐ or ABC‐DLBCL compared with normal GC B cells (total genes on both platforms = 26,438). The lower panel shows GO analysis of genes upregulated by DDR1 in normal GC B cells and also upregulated in both GCB and ABC‐DLBCL. Open bars indicate the percentage of genes present in the GO term that would be expected to be observed in the regulated gene list by chance. Shaded bars indicate the percentage of genes in the regulated list with a given GO term that were actually observed. (B) RT‐qPCR confirming that collagen treatment of DDR1‐expressing GC B cells significantly reduced the mRNA levels of CENPE . Shown are triplicate data on tonsillar GC B cells isolated from three different donors (T20, T21 and T42). (C) Compared to empty vector (EV) control, the addition of collagen significantly reduced CENPE mRNA expression in DDR1‐expressing B‐cell lines, BJAB (maximally after 6 h of stimulation) and DG75 (maximally after 2 h of stimulation). Data are representative of three separate biological replicates. (D) Activation of an ectopically expressed DDR1 reduced CENPE protein expression in both BJAB and DG75 cells. An antibody specific for DDR1 phosphorylated on Tyr792 was used to confirm activation of DDR1. As expected, the activation of DDR1 also reduced total DDR1 levels. β‐Actin was used as a loading control. Data shown are representative of three separate biological replicates. (E) A constitutively activated DDR1 construct also downregulated CENPE protein expression. Shown here are the mean fluorescence intensities for DDR1 and CENPE in DG75 cells transfected with the constitutively active DDR1 gene. Cells expressing DDR1 were significantly more likely to lack CENPE protein expression than were untransfected cells in the same population ( p < 0.0001). (F) Immunohistochemistry showing the downregulation of CENPE protein in DLBCL tumour cells. Top left panel shows strong expression of CENPE protein in a normal germinal centre (GC) of tonsil. Original magnification ×200. Remaining panels show examples of staining in a case in which CENPE was not detected in tumour cells (top right), a case with weak expression in tumour cells (bottom left) and a case showing strong staining (bottom right). Original magnification ×400. Black arrows show tumour cells. Red arrows indicate nonmalignant cells that are positive for CENPE.

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: The Overexpression of Collagen Receptor DDR1 is Associated With Chromosome Instability and Aneuploidy in Diffuse Large B‐Cell Lymphoma

    doi: 10.1111/jcmm.70318

    Figure Lengend Snippet: Activated DDR1 downregulates expression of the mitotic kinesin, CENPE . (A) Upper panels show the significant overlap between genes upregulated by DDR1 in normal GC B cells and those upregulated in either GCB‐ or ABC‐DLBCL compared with normal GC B cells (total genes on both platforms = 26,438). The lower panel shows GO analysis of genes upregulated by DDR1 in normal GC B cells and also upregulated in both GCB and ABC‐DLBCL. Open bars indicate the percentage of genes present in the GO term that would be expected to be observed in the regulated gene list by chance. Shaded bars indicate the percentage of genes in the regulated list with a given GO term that were actually observed. (B) RT‐qPCR confirming that collagen treatment of DDR1‐expressing GC B cells significantly reduced the mRNA levels of CENPE . Shown are triplicate data on tonsillar GC B cells isolated from three different donors (T20, T21 and T42). (C) Compared to empty vector (EV) control, the addition of collagen significantly reduced CENPE mRNA expression in DDR1‐expressing B‐cell lines, BJAB (maximally after 6 h of stimulation) and DG75 (maximally after 2 h of stimulation). Data are representative of three separate biological replicates. (D) Activation of an ectopically expressed DDR1 reduced CENPE protein expression in both BJAB and DG75 cells. An antibody specific for DDR1 phosphorylated on Tyr792 was used to confirm activation of DDR1. As expected, the activation of DDR1 also reduced total DDR1 levels. β‐Actin was used as a loading control. Data shown are representative of three separate biological replicates. (E) A constitutively activated DDR1 construct also downregulated CENPE protein expression. Shown here are the mean fluorescence intensities for DDR1 and CENPE in DG75 cells transfected with the constitutively active DDR1 gene. Cells expressing DDR1 were significantly more likely to lack CENPE protein expression than were untransfected cells in the same population ( p < 0.0001). (F) Immunohistochemistry showing the downregulation of CENPE protein in DLBCL tumour cells. Top left panel shows strong expression of CENPE protein in a normal germinal centre (GC) of tonsil. Original magnification ×200. Remaining panels show examples of staining in a case in which CENPE was not detected in tumour cells (top right), a case with weak expression in tumour cells (bottom left) and a case showing strong staining (bottom right). Original magnification ×400. Black arrows show tumour cells. Red arrows indicate nonmalignant cells that are positive for CENPE.

    Article Snippet: DG75 and BJAB B‐cell lymphoma lines (DSMZ, Braunschweig, Germany) were cultivated in RPMI 1640 (Gibco; Life Technologies Ltd., Paisley, UK) culture media, with 10% FCS and 1% penicillin–streptomycin (Gibco).

    Techniques: Expressing, Quantitative RT-PCR, Isolation, Plasmid Preparation, Control, Activation Assay, Construct, Fluorescence, Transfection, Immunohistochemistry, Staining