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Pep2-8 是 PCSK9 抑制剂,其 KD 值为 0.7 μM,IC50 值为1.4 μM。
生物活性 Pep2-8 is a PCSK9 inhibitor with a binding KD of 0.7 μM and an IC50 of 1.4 μM[1].
细胞效力
(Cellular Effect)Cell Line Type Value Description References HepG2 EC50 6 μM
Reversal of LDL uptake in human HepG2 cells for 2 hrs preincubation with PCSK9 followed by LDL addition and measured after 4 hrs by fluorimetry method relative to control
[PMID: 34266235] LAD2 EC50 > 5 μM
Effect on mast cell degranulation in human LAD2 cells assessed as CCL3 release measured after 2 hrs by Luminex bead based assay
[PMID: 34266235] 体外研究
(In Vitro)Pep2-8 与 C 末端截短的 PCSK9[1]结合。
在 50 μM 的浓度下,Pep2-8 将 PCSK9 处理的 HepG2 细胞的 LDL 摄取恢复到对照活性的约 90%[1]。MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Viability Assay[1]
Cell Line: HepG2 cell. Concentration: 15 μg/mL. Incubation Time: 4 h. Result: Inhibited PCSK9 activity. 体内研究
(In Vivo)Pep2-8 与 C 末端截短的 PCSK9[1]结合。
在 50 μM 的浓度下,Pep2-8 将 PCSK9 处理的 HepG2 细胞的 LDL 摄取恢复到对照活性的约 90%[1]。MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量 1715.85
Formula C83H110N16O24
CAS 号 性状 固体
颜色 White to off-white
Sequence Ac-Thr-Val-Phe-Thr-Ser-Trp-Glu-Glu-Tyr-Leu-Asp-Trp-Val-NH2
Sequence Shortening Ac-TVFTSWEEYLDWV-NH2
运输条件 Room temperature in continental US; may vary elsewhere.
储存方式 Sealed storage, away from moisture and light
Powder -80°C 2 years -20°C 1 year *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
关键词:- DOPE
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产品组分
内容
型号
规格 储存温度
PEP2-8 HY-P2276-01 1mg -20°C PEP2-8 HY-P2276-02 5mg -20°C PEP2-8 HY-P2276-03 10mg -20°C PEP2-8 HY-P2276-04 50mg -20°C PEP2-8 HY-P2276-05 100mg -20°C 操作手册
1 1 常温
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注意事项
保存建议 厂家推荐蓝冰运输。当您收到产品后,按照说明书建议保存于-20°C。 -
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