![Nephrin (NPHS1) Mouse Monoclonal Antibody [Clone ID: LBI1G6]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg)
- ￥653 - 2700
- Leading Biology
- AMM21189V
- 美国
- 2025年07月15日
- WB 1:1000
- Mouse
- Human
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- 详细信息
- 技术资料
- 靶点：
NPHS1
- 浓度：
1 mg/ml
- 应用范围：
WB 1:1000
- 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：
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：
IgG2b
- 免疫原：
Human recombinant protein fragment corresponding to amino acids 1077-1241 of human NPHS1 (NP_004637) produced in E.coli.
- 规格：
100 ul/30 ul
| 规格： | 100 ul | 产品价格： | ￥2700.0 |
|---|---|---|---|
| 规格： | 30 ul | 产品价格： | ￥653.0 |
别名：CNF; nephrin; NPHN
产品概述：NPHS1 mouse monoclonal antibody, clone LBI1G6
总结：This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009]
产品概述：NPHS1 mouse monoclonal antibody, clone LBI1G6
总结：This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009]
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Nephrin (NPHS1) Mouse Monoclonal Antibody [Clone ID: LBI1G6]
￥653 - 2700
