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SV40轉化的非洲綠猴腎細胞C

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更新時間:2025-02-11 18:16:42瀏覽次數:57次

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SV40轉化的非洲綠猴腎細胞COS-7 種屬猴別稱Cos-7;COS7;Cos7;CV-1 inOrigin Simian-7組織來源腎臟疾病轉化細胞系傳代比例/細胞消化1:2傳代 ,消化2-3分鐘培養基配置DMEM培養基

SV40轉化的非洲綠猴腎細胞COS-7

種屬
別稱Cos-7; COS7; Cos7; CV-1 in Origin Simian-7
組織來源腎臟
疾病轉化細胞系
傳代比例/細胞消化1:2傳代 ,消化2-3分鐘
培養基配置DMEM培養基;10%胎牛血清;1%雙抗
簡介COS-7細胞源自CV-1細胞 ,經帶有編碼野生型T抗原的起始失活突變的SV40轉染得到
形態成纖維細胞樣
生長特征貼壁生長
倍增時間~35-48h
基因表達T antigen
培養條件氣相:空氣 ,95% ;二氧化碳 ,5%。 溫度:37攝氏 ,培養箱濕度為70%-80%。
凍存條件凍存液:90%FBS ,DMSO 10%,
或使用非程序凍存液:貨號JY-H040
保藏機構ATCC; CRL-1651
產品使用于科學研究 ,不可作為動物或人類疾病的治療產品使用。

Results: The cohort had a mean age of 39 years and included patients with severe polytrauma. Technical success was achieved in 95% of cases, with no intraoperative deaths or need for open surgical conversion. Perioperative complications were minimal, and the reintervention rate was 5.3%. This study evaluates 10 years of clinical experience managing TAI with TEVAR. Long-term follow-up, with a median duration of 29 months, revealed no graft-related complications or secondary interventions. Imaging confirmed sustained graft integrity, and clinical outcomes were favorable.

Conclusion: TEVAR is a reliable and effective treatment for traumatic aortic injuries, offering excellent technical success rates and minimal perioperative and long-term complications. This study highlights TEVARs advantages in managing polytrauma patients and its role as a minimally invasive alternative to open surgery. Additionally, the findings emphasize the need for comprehensive long-term follow-up protocols. Future research should aim to address challenges related to device durability and the integration of advanced imaging techniques to further enhance patient outcomes and broaden the applicability of TEVAR in trauma care.



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