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编 号 | 规格 | 库存 | 目录价(¥) | 您的价格(¥) | 数 量 |
D360195-0025 | 25 ul | 现货 | 500 | 500 |
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D360195-0100 | 100 ul | 现货 | 1600 | 1600 |
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D360195-0200 | 200 ul | 现货 | 2500 | 2500 |
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概述
The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene.
应用
酶联免疫吸附测定(ELISA),免疫印迹(WB)
属性
保存缓冲液 | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
运输条件 | 2-8°C |
靶点 Uniprot 登记号 | Q8N6F1 |
靶点基因 ID | 149461 |
靶点全称 | claudin 19 |
靶点别名 | HOMG5 |
靶点研究领域 | Signal Transduction |
亚型 | Immunogen-specific rabbit IgG |

