1.Puromycin aminonucleoside-induced nephrosis is a well-described model of human idiopathic nephrotic syndrome, suppressing expression of integrin expression in cultured glomerular epithelial cells.

氨基核苷嘌呤霉素誘導(dǎo)腎病變是人原發(fā)性腎病綜合癥的模型，抑制培養(yǎng)的腎小球上皮細(xì)胞整聯(lián)蛋白的表達(dá)。

2.Puromycin aminonucleoside-induced nephrosis is a well-described model of human idiopathic nephrotic syndrome, suppressing expression of integrin expression in cultured glomerular epithelial cells.

氨基核苷嘌呤霉素誘導(dǎo)腎病變是人原發(fā)性腎病綜合癥的模型，抑制培養(yǎng)的腎小球上皮細(xì)胞整聯(lián)蛋白的表達(dá)。

3.While the salt shares the same pharmacological properties as puromycin free base, its greater water solubility may offer advantages in some in vitro applications.

該鹽同嘌呤霉素游離堿具有相同的藥理學(xué)性質(zhì)，它的高度的水溶性能給體外研究應(yīng)用提供一些優(yōu)勢(shì)。

4.Puromycin is used in cell biology to select mammalian cell lines that have been transformed by vectors that express puromycin-N-acetyl-transferase.

在細(xì)胞生物學(xué)中用嘌羅霉素來選擇用載體轉(zhuǎn)化能表達(dá)嘌呤霉素- N -乙酰基轉(zhuǎn)移酶類的哺乳動(dòng)物細(xì)胞系。

5.Puromycin aminonucleoside is the key intermediate in the synthesis of semi-synthetic analogues of puromycin.

氨基核苷嘌呤霉素是合成嘌呤毒素的半合成類似物中關(guān)鍵性的中間體。