山羊乳腺上皮細胞永生化細胞
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- 公司名稱 上海富雨生物科技有限公司
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山羊乳腺上皮細胞永生化
19156044901 (同微信)
deplete the precursor tryptophan. In this review, we summarize the current knowledge on the immune tumour microenvironlknt of neuroendocrine tumours and implications for treatlknt with immune checkpoint inhibitors. We also discuss (targetable) factors in the NET tumour microenvironlknt that potentially modulate the anti-cancer
system. Their expression, activity, and subcellular localization are associated with the distinct development and differentiation stages of immune cells. They promote the activation of innate myeloid immune cells since they contribute to toll-like receptor signaling and to cytokine secretion. Furthermore, they control lysosomal biogenesis and autophagic flux, thus affecting
種屬 | 羊 |
組織來源 | 正常乳腺組織 |
傳代比例 | 1:2傳代 |
培養(yǎng)基配置 | 基礎(chǔ)培養(yǎng)基500ml ;生長添加劑5ml ;胎牛血清10ml ;雙抗5ml |
簡介 | 乳腺位于皮下淺筋膜的淺層與深層之間。淺筋膜伸向乳腺組織內(nèi)形成條索狀的小葉間隔 ,一端連于胸肌筋膜 ,另一端 連于皮膚 ,將乳腺腺體固定在胸部的皮下組織之中。乳房腺體由15-20個腺葉組成 ,每一腺葉分成若干個腺小葉 ,每 一腺小葉又由10-100個腺泡組成 ,這些腺泡緊密地排列在小乳管周圍 ,腺泡的開口與小乳管相連 ,乳腺上皮細胞來源 于乳腺小葉中。它們與腺體導(dǎo)管和脂肪組織一起在乳腺中形成復(fù)雜的網(wǎng)絡(luò)結(jié)構(gòu)。乳腺上皮細胞在人和動物體出生、發(fā) 育和妊娠中均會受荷爾蒙調(diào)控而進行一系列的增長、遷移和分化。激素水平失調(diào)、細胞外基質(zhì)的變化和其它的基因因 素都會導(dǎo)致乳腺上皮細胞惡性增長 ,最終導(dǎo)致乳腺癌的發(fā)生。了解乳腺上皮細胞的特性可以幫助我們理解乳腺癌的病 例機制以及為治療確定新的靶點。 |
形態(tài) | 上皮細胞樣 ,多角形細胞樣 |
生長特征 | 貼壁生長 |
細胞檢測 | 細胞角蛋白-18( CK-18 )免疫熒光染色為陽性免疫熒光鑒定 ,細胞純度可達90%以上 ,不含有HIV-1、HBV、 HCV、支原體、細菌、酵母和真菌等。 |
倍增時間 | 每周 2 至 3 次 |
備注 | 山羊乳腺上皮細胞永生化該細胞通過慢病毒轉(zhuǎn)染的方式攜帶SV40基因。 |

19156044901 (同微信)
deplete the precursor tryptophan. In this review, we summarize the current knowledge on the immune tumour microenvironlknt of neuroendocrine tumours and implications for treatlknt with immune checkpoint inhibitors. We also discuss (targetable) factors in the NET tumour microenvironlknt that potentially modulate the anti-cancer
system. Their expression, activity, and subcellular localization are associated with the distinct development and differentiation stages of immune cells. They promote the activation of innate myeloid immune cells since they contribute to toll-like receptor signaling and to cytokine secretion. Furthermore, they control lysosomal biogenesis and autophagic flux, thus affecting