![LMAN1 Mouse Monoclonal Antibody [Clone ID: LBI1A8]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg)
- ￥690 - 2025
- Leading Biology
- AMM10640V
- 美国
- 2025年07月10日
- WB 1:200~500, IHC 1:150, IF 1:100, FLOW 1:100
- Mouse
- Human, Monkey, Mouse, Rat, Dog
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- 详细信息
- 技术资料
- 靶点：
LMAN1
- 浓度：
1 mg/ml
- 应用范围：
WB 1:200~500, IHC 1:150, IF 1:100, FLOW 1:100
- 宿主：
Mouse
- 适应物种：
Human, Monkey, Mouse, Rat, Dog
- 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：
Store at +4°C short term. 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：
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
- 亚型：
IgG1
- 免疫原：
Full length human recombinant protein of human LMAN1 (NP_005561) produced in HEK293T cell.
- 规格：
100 ul/30 ul
| 规格： | 100 ul | 产品价格： | ￥2025.0 |
|---|---|---|---|
| 规格： | 30 ul | 产品价格： | ￥690.0 |
别名：ERGIC-53; ERGIC53; F5F8D; FMFD1; gp58; MCFD1; MR60
产品概述：LMAN1 mouse monoclonal antibody, clone LBI1A8
总结：The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished. [provided by RefSeq]
产品概述：LMAN1 mouse monoclonal antibody, clone LBI1A8
总结：The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished. [provided by RefSeq]
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LMAN1 Mouse Monoclonal Antibody [Clone ID: LBI1A8]
￥690 - 2025
