![Apolipoprotein E (APOE) Mouse Monoclonal Antibody [Clone ID: LBI3F1]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg)
- ￥3300
- Leading Biology
- AMM16896VCF
- 美国
- 2025年07月12日
- WB 1:2000, IHC 1:150
- Mouse
- Human
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- 详细信息
- 技术资料
- 靶点：
APOE
- 应用范围：
WB 1:2000, IHC 1:150
- 宿主：
Mouse
- 适应物种：
Human
- 保质期：
1-2年
- 供应商：
安诺伦（北京）生物科技有限公司
- 标记物：
Unconjugated
- 克隆性：
Monoclonal Antibody
- 保存条件：
Stable for 1 year at -20°C from date of shipment. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
- 形态：
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
- 亚型：
IgG2b
- 免疫原：
Full length human recombinant protein of human APOE (NP_000032) produced in HEK293T cell.
- 规格：
100 ug
别名：AD2; APO-E; LDLCQ5; LPG
产品概述：Carrier-free (BSA/glycerol-free) APOE mouse monoclonal antibody, clone LBI3F1
总结：Chylomicron remnants and very low density lipoprotein (VLDL) remnants are rapidly removed from the circulation by receptor-mediated endocytosis in the liver. Apolipoprotein E, a main apoprotein of the chylomicron, binds to a specific receptor on liver cells and peripheral cells. ApoE is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. The APOE gene is mapped to chromosome 19 in a cluster with APOC1 and APOC2. Defects in apolipoprotein E result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. [provided by RefSeq, Jul 2008]
产品概述：Carrier-free (BSA/glycerol-free) APOE mouse monoclonal antibody, clone LBI3F1
总结：Chylomicron remnants and very low density lipoprotein (VLDL) remnants are rapidly removed from the circulation by receptor-mediated endocytosis in the liver. Apolipoprotein E, a main apoprotein of the chylomicron, binds to a specific receptor on liver cells and peripheral cells. ApoE is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. The APOE gene is mapped to chromosome 19 in a cluster with APOC1 and APOC2. Defects in apolipoprotein E result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. [provided by RefSeq, Jul 2008]
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Apolipoprotein E (APOE) Mouse Monoclonal Antibody [Clone ID: LBI3F1]
￥3300
