<tr id="iswe0"><td id="iswe0"></td></tr>
<ul id="iswe0"><thead id="iswe0"></thead></ul>

  • 大又大粗又爽又黄少妇毛片,髙清无码一级爱a视频,波多野结衣av家庭教师在线播放,人妻少妇精品久久久久久0000,久久热这里有精品,亚洲中文字幕精品一区,国产AV无码亚洲AV无码,亚洲最新色情图域名午夜
    技術文章您的位置:網站首頁 >技術文章 > Zeta Life轉染原代奶牛子宮內膜上皮細胞(BEECs)發表文章
    Zeta Life轉染原代奶牛子宮內膜上皮細胞(BEECs)發表文章
    更新時間:2022-04-06   點擊次數:814次

     

     

     

     

    一、發表文章轉染簡述:

    文章使用美國Zeta Life公司,#Advanced DNA RNA轉染試劑(#AD600150,Zeta Life, USA) 將構建的pCMV-GSDMD-N-HA 載體質粒DNA(圖 6A)轉染到原代奶牛子宮內膜上皮細胞(BEECs), 48小時后用Western blotting檢測GSDMD,并檢測到蛋白表達確定轉染成功(圖 6B)。

    重建細胞炎癥模型,提取總蛋白,GSDMD表達及其裂解的N使用蛋白質印跡法檢測末端蛋白。結果表明 BEEC 暴露于 LPS(10 和 30 µg/ml)24 小時可以裂解 GSDMD 并導致焦亡(圖 6C)

    文章標題LPS Mediates Bovine Endometrial Epithelial Cell Pyroptosis Directly Through Both NLRP3 Classical and Non-Classical Inflflammasome Pathways。

    發表文章單位:中國農業科學院畜牧與藥學研究所,農業農村部獸藥開發重點實驗室,蘭州研究所。

    二、轉染原代上皮細胞(BEECs)部分論文欣賞

    1、LPS Exposure for 24 h Leads to BEEC Inflflammation and Cleaved GSDMD to Pyroptosis

    We constructed a pCMV-GSDMD-N-HA vector (Figure 6A) and transfected it to BEECs to overexpress GSDMD, and detected protein expression withWestern blotting after 48 h to ensure the transfection was successful (Figure 6B). The cell inflflammation model was rebuilt,

    total proteinwas extracted, and GSDMD expression and its cleaved N terminal protein were detected using Western blotting. The resultsshowed that BEEC exposed to LPS (10 and 30 µg/ml) for 24 h could cleave GSDMD and lead to pyroptosis (Figure 6C).

    2、Genetic Recombination

    Genetic Recombination Technology was adopted to ligate bovine GSDMD DNA fragments into the ampicillin-resistant pCMV-HA vector and transform it into E. coli. Brieflfly, the bacteria were grown on an LB agar medium containing ampicillin sodium for 24 h at 37°C. A single colony was picked and added to the LB liquid medium containing ampicillin sodium and culturedfor 16 h at 37°C with shaking at 300×g. Plasmid DNA was extracted with an Endo[1]free Plasmid Mini Kit I and quantifified using a Polluton100+. The Zeta Life Transfection Kit was used to transfect the plasmid into BEECs, and LPSwas used to construct the cell inflflammation model. The cell total protein was extracted and detected by an HA tag and Western blotting to evaluate the GSDMD protein expression and its cleavage during cell pyroptosis. The vector construction, restriction endonuclease cleavage verifification, and sequencing verifification were done by Genecreate Biological Company。

    三、Zeta Life 公司與美國加利福尼亞大學舊金山校區聯合開發用于哺乳動物細胞、活體動物轉染的 Advanced DNA RNA 第三代多肽小分子轉染試劑,此技術成為新的蛋白功能、免疫細胞及干細胞治療、研發及生產的主要關鍵技術之一。

    <i class="backsohu" data:image="" png;base64,ivborw0kggoaaaansuheugaaaa4aaaaocayaaaafsc3raaaagxrfwhrtb2z0d2fyzqbbzg9izsbjbwfnzvjlywr5ccllpaaaayjpvfh0we1momnvbs5hzg9izs54bxaaaaaaadw="" ehbhy2tldcbizwdpbj0i77u="" 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"" pjuuod0aaakhsurbvhjavjjdsbrrfmf="" d="" aos7szq7hufiunrlaukqhkuojcqr8vgufzix08geied0h5id1veptxavkkqfasycrkeag+ha9bwghjouuirk5k5dbozm7o6exupxrh4j4z53fu="" f="" pfznnabusu+clkicq5jf4fxhgzofcjvdcb7mzdmgngdqari0bpefdp4sgvoon0pkie9cauehhq1wgeeqdsm1wvs4adfrelcj5nkh3rjdsqhqn96+mq60ldltnr0yozhgelp+j0sikyjsd5zkcsiugp3enqkhtrloag9phtkqrruiagqmh="" c1x="" mfq="" wvgfbgu="" 2soal5yeosbgays8v2y+ayl9smjjjtvmjgedjsx3k1ifv6jpdzc29rsslcm4c30dtx67ka6sgsp5cb9ale7js72cadl9shingnyrtagle+c4uokg0qyluh6nyd8qyxo7ca9wq+ivkuxngch="" wak9izsgvfkgfdslyro0hck10cogqhrbooaxpt3aj1dzfg8v4re0nfw9fdbwzwvolnxmj07xu="" lyt+d3kvt60ecjoyv6jkb4kp9vl8ntu9gi0tzrxoe+xkwjzxofaq2vsgedpurnfzdsuoi3laq4xmbldvq1+2hlryblw0432blbqkdt1tchpri="" xaqkxxg6apulppwjead0civozufvlaxflbguf3fdowmsmuv5ocssbqef4g9ohokoe3ft6tp5bp+cpodld1mkn3bs7x0notduylwhnrum0wp+mw0uzjel2nxljgzmyd2ulwxpnuspb4gko1oztlvqecvnjowpmnqumh6dcpupc9s6r+5gk6qtg1gi59jy1i1leortsjciz8cdaczhh="" u4gnf4aaaaabjru5erkjggg="=")" center="" no-repeat;="" display:="" inline-block;="" vertical-align:="" top;"="" style="box-sizing: border-box; margin: 0px 5px 0px 0px; border: 0px; padding: 0px; width: 15px; height: 15px; background-image: url(""); background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial;">

     

     

    ©2025  上海創凌生物科技有限公司 All Rights Reserved.  網站地圖  滬ICP備2023009255號-1  管理登陸  技術支持:化工儀器網
    在線客服 二維碼

    掃一掃,關注我們

    主站蜘蛛池模板: 天堂√在线中文最新版8| 无码人妻丰满熟妇精品区东京直播| 亚洲品质极品自拍极速福利在线| 免费人成在线观看网站| 云霄县| 人妻在线日韩免费视频| 人妻精品动漫H| 越南小少妇bbwbbwbbw| 人人草人人做人人爱| 欧产日产国产精品精品| 粉嫩小泬无遮挡久久久久久 | 一卡2卡三卡4卡免费网站| 精品无码无码一级毛片免费| 国产一区二区三区三区| 桦甸市| 国产精品成人自产拍在线| 无人视频在线观看播放免费| 亚洲综合精品网站| 国产亚洲成av片在线观看| 中文字幕人妻系列人妻 无码| 青青青在线观看国产大片| 337p日本大胆欧美人视| 在线一区二区三区一本到| 人妻少妇精品一区二区三区| 五月丁香六月综合缴清无码| 国产自产一区二区三区视频| 一本久久a久久精品综合香蕉| 91久久澡人人爽人人添| 精品人妻系列无码人妻免费视频| 婷婷六月丁香午夜爱爱| 国产成人免费an| 牛仔裤美女国产精品毛片 | 中文字字幕在中文无码| 少妇粉嫩小泬喷水视频WWW| 无码人妻AⅤ一区二区三区夏目| 特级国产午夜理论不卡| 伊人久久大香线蕉av色婷婷色| 精品国产污污免费网| 老湿机69福利区无码福利网| 中国国产免费毛卡片| 精品无码人妻被多人侵犯AV|