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Detachabead cd19 kit

Manufactured by Thermo Fisher Scientific

The DETACHaBEAD CD19 kit is a laboratory product designed for the isolation and enrichment of CD19-positive cells from a variety of biological samples. The kit utilizes magnetic beads coated with anti-CD19 antibodies to capture and separate the target cells.

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2 protocols using detachabead cd19 kit

1

Isolation and Culture of EBV-associated Cells

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Cell lines include EBV-positive Raji cells (ATCC CCL-86) [59 (link)], EBV-negative Elijah B cells (kindly provided by Prof. A.B. Rickinson), 293 cells (ATCC CRL-1573) [60 (link)], T cells specific for EBNA1 3E10, EBNA3C 5H11, gp350 1D6 and BNRF1 VSD epitopes (kindly provided by Prof. J. Mautner) and autologous LCLs (kindly provided by Prof. J. Mautner). Peripheral blood mononuclear cells (PBMCs) were isolated using Ficoll-Paque Plus and primary B cells were isolated using Dynabeads CD19 Pan B (Invitrogen) and DETACHaBEAD CD19 kit (Invitrogen). RPMI containing 10% fetal calf serum (F7524, Sigma) was used to culture 293, Raji and Elijah cells. T-cell clones and lines were cultured as previously described [17 (link),35 (link)].
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2

Prognostic Value of circCTNNA1 in MCL

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This study enrolled a total of 56 MCL patients (34 cases of blastoid variant and 22 cases of pleomorphic variant; 63.4+/−6,6 years; 32 males and 24 females) and 56 healthy controls (63.5+/−6,5 years; 32 males and 24 females) at Zibo Central Hospital from May 2014 to May 2016. Ethics approval was obtained from the Ethics Committee of this hospital. Two groups of participants showed similar distributions of age and gender. The diagnosis of MCL was performed according to WHO classification of hematological neoplasms. Patients with leukemic phase MCL were excluded from this study. Fasting blood samples were collected from both groups of participants prior to the initiation of therapies. DETACHaBEAD CD19 Kit (Invitrogen) was used to separate B lymphocytes from all blood samples. Purity of higher than 90% was reached in all samples of B lymphocytes. All patients signed the informed consent. MCL patients were treated with chemoimmunotherapy R-CHOP, in which rituximab, cyclophosphamide, hydroxydaunomycin, vincristine sulfate and prednisone were included.
All 56 MCL patients were followed up for 5 years to evaluate the prognostic value of circCTNNA1 for MCL. Patients were visited through outpatient visit and telephone in some cases. All patients either died of MCL or survived until the end of follow-up. This study was conducted in accordance with the Declaration of Helsinki.
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