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CD8+ TCR Knockout NFAT-Luciferase Reporter Jurkat Cell Line 返回列表頁(yè)

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更新時(shí)間：2023-10-12 09:14:47瀏覽次數(shù)：196次

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數(shù)量：1供應(yīng)商：BPSBioscience細(xì)胞類型：穩(wěn)轉(zhuǎn)細(xì)胞系品系：Jurkat(cloneE6-1)

詳情介紹

數(shù)量：
1
供應(yīng)商：
BPS Bioscience
細(xì)胞類型：
穩(wěn)轉(zhuǎn)細(xì)胞系
品系：
Jurkat (clone E6-1), human T lymphoblast, suspension
組織來(lái)源：
/
相關(guān)疾病：
多種
免疫類型：
多種
器官來(lái)源：
無(wú)
運(yùn)輸方式：
干冰
年限：
10
生長(zhǎng)狀態(tài)：
良好
CAS號(hào)：
無(wú)
英文名：
CD8+ TCR Knockout NFAT-Luciferase Reporter Jurkat Cell Line
注冊(cè)證號(hào)：
/
規(guī)格：
2管

This cell line was generated from TCR Knockout NFAT Luciferase Reporter Jurkat Cell Line (BPS Bioscience #78556) by exogeneous overexpression of human CD8 (NM_001768.6) using lentiviral transduction (CD8a Lentivirus, BPS Bioscience #78648). To achieve knockout of TCR (T Cell Receptor), the TRAC (T-Cell Receptor Alpha Constant) and TRBC1 (T-Cell Receptor Beta Constant 1) domains of the TCRα/β chains were genetically removed by CRISPR/Cas9 genome editing from recombinant Jurkat cells stably expressing the firefly luciferase gene under the control of NFAT response elements.TCRα/β knockout in the TCR Knockout NFAT-Luciferase Reporter Jurkat cells was confirmed by genomic sequencing and by flow cytometry and expression of CD8 was confirmed by flow cytometry. The cell line has been functionally validated and does not respond to anti-CD3 agonist antibodies, as opposed to parental NFAT-Luciferase Reporter Jurkat cells (BPS Bioscience #60621).