huvecs 中文意思是什麼

huvecs 解釋
臍靜脈
  1. The expression ratios reported are the average from the two separate experiments. ( 1 ) huvecs exposed to fluid shear stress ( 4. 20 dyne / cm2 ) for 1 h, 2 h, 3 h, 4 h, 5 h, 6 h, 7 h, 8 h, 9 h, 10 h, or 12 h, respectively

    735x10 』拷貝,與3h時的表達量處在同一個數量級;在7dh之間h七inrna的表達量相對穩定,但和4 ? 6h之間n
  2. ( 4 ) huvecs exposed to low fluid shear stress ( 4. 20 dyne / cm " ) for 2 h and incubated by 17 p - estradiol ( 10 - 7 m ) + low shear stress ( 4. 20 dyne / cm2, 2 h ). normal static cultured huvecs were selected as a control

    929x10 』拷貝之間,和44h之間neinrna的表達量相比又下降了一個數量級;未用切應力處理的內皮細胞沒有il七基因的表達,基線值分別為8
  3. Objective to investigate the effects of fluid shear stress on il - 8 gene in human umbilical vein endothelial cells ( huvecs ) and the roles of time course of low shear stress and intensity of fluid shear stress using lightcycler ? system ; to investigate the gene expression profiles in huvecs exposed on low shear stress ( 4. 20 dyne / cm2, 2 h ) and incubated by 17 p - estradiol ( 10 - 7 m ) + low shear stress ( 4. 20 dyne / cm2, 2 h ) using the cdna microarray approach. methods endothelial cells were isolated from human umbilical cord veins by collagenase treatment as described by jaffe and modified

    目的探討人臍靜脈內皮細胞( humanumbilicalveinendothelialcells , huvecs )在流體切應力作用下il - 8基因的誘導表達以及切應力的作用時間和作用強度對il - 8基因表達影響的變化規律;利用表達譜基因晶元技術研究內皮細胞在低切應力( 4 . 20dyne cm ~ 2 , 2h )作用下其切應力相關基因的表達情況以及生理濃度( 10 ~ ( - 7 )的17 -雌二醇孵育內皮細胞48h ,再經同樣條件的切應力處理后對內皮細胞切應力相關基因表達的可能影響。
  4. Methods human umbilical vein endothelial cells ( huvecs ) were cultured in vitro

    方法體外培養人臍靜脈內皮細胞,通過傳代形成細胞的衰老模型。
  5. The fluid used to shear huvecs was the cultured medium

    以未作任何處理的內皮細胞為陰性對照。
  6. Hsvecs and huvecs angiogenesis model in vitro

    血管生成模型的比較
  7. Results ( 1 ) el - 8 mrna did not express in huvecs untreated with fluid shear stress

    23dyne兒m勺時k七inrna表達量時為1
  8. Arsenic trioxide induces apoptosis in huvecs and inhihits angiogenesis in cam

    三氧化二砷誘導血管內皮細胞凋亡和抑制血管生成的研究
  9. First of all, we stimulate the huvec with lps ( 50ug / ml ) to observe the damage of cells. we find that lps was able to induce apoptosis of huvecs in a time - dependent fashion

    結果發現, lps加入細胞培養中可明顯誘導huvec的凋亡,並隨著作用時間的延長,細胞凋亡率也相應增加。
分享友人