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lymphoma jijoye cell line ccl87 american type culture collection  (ATCC)


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    ATCC lymphoma jijoye cell line ccl87 american type culture collection
    Figure 3: Exposure of peripheral blood mononuclear cells (PBMC) from patients with acute lymphoblastic leukemia in remission / long term survivors(ALL) and sickle cell disease (SCD) to the culture media, plasma, avian leucosis virus, Mycocladus Corymbifera, aflatoxin, supernatant of CRL-2312 cell line culture, supernatant of culture of Aspergillus Flavus obtained from a home of a patient with acute lymphoblastic leukemia, Supernatant of <t>CCL87</t> culture which contains EBV, supernatant of culture of Aspergillus Flavus co-cultured with purified Epstein Barr Virus (EBV) and purified EBV alone. Samples were analyzed for cell surface phenotype using flow cytometry every 24 hours for four days. Each day, samples were tested for CD10/CD19, CD34/CD19 and CD34/ CD117. Results were recorded as percentage of control. Aflatoxin indiscriminately induced abnormal cell surface phenotypes, both, in PBMC of ALL patients as well those of sickle cell disease controls. Supernatant of culture of Aspergillus Flavus, with and without EBV, and CCL87 or EBV alone induced positive cell surface
    Lymphoma Jijoye Cell Line Ccl87 American Type Culture Collection, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 59 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lymphoma+cell+line+jijoye/Jiyoye/pm33348275-127-8-13
    Average 94 stars, based on 59 article reviews
    lymphoma jijoye cell line ccl87 american type culture collection - by Bioz Stars, 2026-10
    94/100 stars

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    1) Product Images from "Exposure to a mycovirus containing Aspergillus Flavus reproduces acute lymphoblastic leukemia cell surface and genetic markers in cells from patients in remission and not controls."

    Article Title: Exposure to a mycovirus containing Aspergillus Flavus reproduces acute lymphoblastic leukemia cell surface and genetic markers in cells from patients in remission and not controls.

    Journal: Cancer treatment and research communications

    doi: 10.1016/j.ctarc.2020.100279

    Figure 3: Exposure of peripheral blood mononuclear cells (PBMC) from patients with acute lymphoblastic leukemia in remission / long term survivors(ALL) and sickle cell disease (SCD) to the culture media, plasma, avian leucosis virus, Mycocladus Corymbifera, aflatoxin, supernatant of CRL-2312 cell line culture, supernatant of culture of Aspergillus Flavus obtained from a home of a patient with acute lymphoblastic leukemia, Supernatant of CCL87 culture which contains EBV, supernatant of culture of Aspergillus Flavus co-cultured with purified Epstein Barr Virus (EBV) and purified EBV alone. Samples were analyzed for cell surface phenotype using flow cytometry every 24 hours for four days. Each day, samples were tested for CD10/CD19, CD34/CD19 and CD34/ CD117. Results were recorded as percentage of control. Aflatoxin indiscriminately induced abnormal cell surface phenotypes, both, in PBMC of ALL patients as well those of sickle cell disease controls. Supernatant of culture of Aspergillus Flavus, with and without EBV, and CCL87 or EBV alone induced positive cell surface
    Figure Legend Snippet: Figure 3: Exposure of peripheral blood mononuclear cells (PBMC) from patients with acute lymphoblastic leukemia in remission / long term survivors(ALL) and sickle cell disease (SCD) to the culture media, plasma, avian leucosis virus, Mycocladus Corymbifera, aflatoxin, supernatant of CRL-2312 cell line culture, supernatant of culture of Aspergillus Flavus obtained from a home of a patient with acute lymphoblastic leukemia, Supernatant of CCL87 culture which contains EBV, supernatant of culture of Aspergillus Flavus co-cultured with purified Epstein Barr Virus (EBV) and purified EBV alone. Samples were analyzed for cell surface phenotype using flow cytometry every 24 hours for four days. Each day, samples were tested for CD10/CD19, CD34/CD19 and CD34/ CD117. Results were recorded as percentage of control. Aflatoxin indiscriminately induced abnormal cell surface phenotypes, both, in PBMC of ALL patients as well those of sickle cell disease controls. Supernatant of culture of Aspergillus Flavus, with and without EBV, and CCL87 or EBV alone induced positive cell surface

    Techniques Used: Clinical Proteomics, Virus, Cell Culture, Purification, Flow Cytometry, Control

    Related Articles

    Comparison:

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: Cell lines and virus production.Cell lines and virus production.. The EBV-2-positive Burkitt’s lymphoma cell line Jijoye (P-2003, P-3J; ATCC, Manassas, VA) and the EBV-negative cell line BL41 (gift of J. Sixbey, St. Jude Children's Research Hospital) were maintained in complete RPMI at 37°C and 5% CO 2 .. The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: The EBV-2-positive Burkitt’s lymphoma cell line Jijoye (P-2003, P-3J; ATCC, Manassas, VA) and the EBV-negative cell line BL41 (gift of J. Sixbey, St. Jude Children's Research Hospital) were maintained in complete RPMI at 37°C and 5% CO 2 .. The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: 116 117 on A pril 9, 2020 at U niversity of B irm ingham http://jvi.asm .org/ D ow nloaded from 7 Cell lines and virus production.116 117 on A pril 9, 2020 at U niversity of B irm ingham http://jvi.asm .org/ D ow nloaded from 7 Cell lines and virus production.. The EBV-2 positive Burkitt’s lymphoma cell line Jijoye (P-118 2003, P-3J, ATCC Manassas, VA) and the EBV negative cell line BL41 (gift of J. Sixbey, St. 119 Judes) were maintained in complete RPMI at 37C and 5% CO2.. Jurkat T cell line (American 120 Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10mM 121 HEPES.Jurkat T cell line (American 120 Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10mM 121 HEPES.

    Sequencing:

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: Cell lines and virus production.Cell lines and virus production.. The EBV-2-positive Burkitt’s lymphoma cell line Jijoye (P-2003, P-3J; ATCC, Manassas, VA) and the EBV-negative cell line BL41 (gift of J. Sixbey, St. Jude Children's Research Hospital) were maintained in complete RPMI at 37°C and 5% CO 2 .. The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: The EBV-2-positive Burkitt’s lymphoma cell line Jijoye (P-2003, P-3J; ATCC, Manassas, VA) and the EBV-negative cell line BL41 (gift of J. Sixbey, St. Jude Children's Research Hospital) were maintained in complete RPMI at 37°C and 5% CO 2 .. The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: 116 117 on A pril 9, 2020 at U niversity of B irm ingham http://jvi.asm .org/ D ow nloaded from 7 Cell lines and virus production.116 117 on A pril 9, 2020 at U niversity of B irm ingham http://jvi.asm .org/ D ow nloaded from 7 Cell lines and virus production.. The EBV-2 positive Burkitt’s lymphoma cell line Jijoye (P-118 2003, P-3J, ATCC Manassas, VA) and the EBV negative cell line BL41 (gift of J. Sixbey, St. 119 Judes) were maintained in complete RPMI at 37C and 5% CO2.. Jurkat T cell line (American 120 Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10mM 121 HEPES.Jurkat T cell line (American 120 Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10mM 121 HEPES.

    Binding Assay:

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: Cell lines and virus production.Cell lines and virus production.. The EBV-2-positive Burkitt’s lymphoma cell line Jijoye (P-2003, P-3J; ATCC, Manassas, VA) and the EBV-negative cell line BL41 (gift of J. Sixbey, St. Jude Children's Research Hospital) were maintained in complete RPMI at 37°C and 5% CO 2 .. The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: The EBV-2-positive Burkitt’s lymphoma cell line Jijoye (P-2003, P-3J; ATCC, Manassas, VA) and the EBV-negative cell line BL41 (gift of J. Sixbey, St. Jude Children's Research Hospital) were maintained in complete RPMI at 37°C and 5% CO 2 .. The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.The Jurkat T cell line (American Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10 mM HEPES.

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells
    Article Snippet: 116 117 on A pril 9, 2020 at U niversity of B irm ingham http://jvi.asm .org/ D ow nloaded from 7 Cell lines and virus production.116 117 on A pril 9, 2020 at U niversity of B irm ingham http://jvi.asm .org/ D ow nloaded from 7 Cell lines and virus production.. The EBV-2 positive Burkitt’s lymphoma cell line Jijoye (P-118 2003, P-3J, ATCC Manassas, VA) and the EBV negative cell line BL41 (gift of J. Sixbey, St. 119 Judes) were maintained in complete RPMI at 37C and 5% CO2.. Jurkat T cell line (American 120 Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10mM 121 HEPES.Jurkat T cell line (American 120 Type Culture Collection, Baltimore, MD) was maintained in complete RPMI with 10mM 121 HEPES.



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    Figure 3: Exposure of peripheral blood mononuclear cells (PBMC) from patients with acute lymphoblastic leukemia in remission / long term survivors(ALL) and sickle cell disease (SCD) to the culture media, plasma, avian leucosis virus, Mycocladus Corymbifera, aflatoxin, supernatant of CRL-2312 cell line culture, supernatant of culture of Aspergillus Flavus obtained from a home of a patient with acute lymphoblastic leukemia, Supernatant of <t>CCL87</t> culture which contains EBV, supernatant of culture of Aspergillus Flavus co-cultured with purified Epstein Barr Virus (EBV) and purified EBV alone. Samples were analyzed for cell surface phenotype using flow cytometry every 24 hours for four days. Each day, samples were tested for CD10/CD19, CD34/CD19 and CD34/ CD117. Results were recorded as percentage of control. Aflatoxin indiscriminately induced abnormal cell surface phenotypes, both, in PBMC of ALL patients as well those of sickle cell disease controls. Supernatant of culture of Aspergillus Flavus, with and without EBV, and CCL87 or EBV alone induced positive cell surface
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    Figure 3: Exposure of peripheral blood mononuclear cells (PBMC) from patients with acute lymphoblastic leukemia in remission / long term survivors(ALL) and sickle cell disease (SCD) to the culture media, plasma, avian leucosis virus, Mycocladus Corymbifera, aflatoxin, supernatant of CRL-2312 cell line culture, supernatant of culture of Aspergillus Flavus obtained from a home of a patient with acute lymphoblastic leukemia, Supernatant of CCL87 culture which contains EBV, supernatant of culture of Aspergillus Flavus co-cultured with purified Epstein Barr Virus (EBV) and purified EBV alone. Samples were analyzed for cell surface phenotype using flow cytometry every 24 hours for four days. Each day, samples were tested for CD10/CD19, CD34/CD19 and CD34/ CD117. Results were recorded as percentage of control. Aflatoxin indiscriminately induced abnormal cell surface phenotypes, both, in PBMC of ALL patients as well those of sickle cell disease controls. Supernatant of culture of Aspergillus Flavus, with and without EBV, and CCL87 or EBV alone induced positive cell surface

    Journal: Cancer treatment and research communications

    Article Title: Exposure to a mycovirus containing Aspergillus Flavus reproduces acute lymphoblastic leukemia cell surface and genetic markers in cells from patients in remission and not controls.

    doi: 10.1016/j.ctarc.2020.100279

    Figure Lengend Snippet: Figure 3: Exposure of peripheral blood mononuclear cells (PBMC) from patients with acute lymphoblastic leukemia in remission / long term survivors(ALL) and sickle cell disease (SCD) to the culture media, plasma, avian leucosis virus, Mycocladus Corymbifera, aflatoxin, supernatant of CRL-2312 cell line culture, supernatant of culture of Aspergillus Flavus obtained from a home of a patient with acute lymphoblastic leukemia, Supernatant of CCL87 culture which contains EBV, supernatant of culture of Aspergillus Flavus co-cultured with purified Epstein Barr Virus (EBV) and purified EBV alone. Samples were analyzed for cell surface phenotype using flow cytometry every 24 hours for four days. Each day, samples were tested for CD10/CD19, CD34/CD19 and CD34/ CD117. Results were recorded as percentage of control. Aflatoxin indiscriminately induced abnormal cell surface phenotypes, both, in PBMC of ALL patients as well those of sickle cell disease controls. Supernatant of culture of Aspergillus Flavus, with and without EBV, and CCL87 or EBV alone induced positive cell surface

    Article Snippet: Another source of EBV was Type 2 Burkitt‟s lymphoma Jijoye cell line (CCL87) (American Type Culture Collection (ATCC), Monassas, VA).

    Techniques: Clinical Proteomics, Virus, Cell Culture, Purification, Flow Cytometry, Control

    Comparison of gp350 amino acid sequences. The amino acid sequence (amino acids 1 to 504) of the gp350 protein of the EBV-1 strain Akata is shown. The known CD21 binding regions are underlined. The amino acid differences in gp350 of the EBV-2 strain Jijoye are in bold above the EBV-1 sequence.

    Journal: Journal of Virology

    Article Title: CD21 (Complement Receptor 2) Is the Receptor for Epstein-Barr Virus Entry into T Cells

    doi: 10.1128/JVI.00428-20

    Figure Lengend Snippet: Comparison of gp350 amino acid sequences. The amino acid sequence (amino acids 1 to 504) of the gp350 protein of the EBV-1 strain Akata is shown. The known CD21 binding regions are underlined. The amino acid differences in gp350 of the EBV-2 strain Jijoye are in bold above the EBV-1 sequence.

    Article Snippet: The EBV-2-positive Burkitt’s lymphoma cell line Jijoye (P-2003, P-3J; ATCC, Manassas, VA) and the EBV-negative cell line BL41 (gift of J. Sixbey, St. Jude Children's Research Hospital) were maintained in complete RPMI at 37°C and 5% CO 2 .

    Techniques: Comparison, Sequencing, Binding Assay