产品货号：
Z20392
中文名称：
MFAP1抗体
英文名称：
Anti-MFAP1 Antibody
产品规格：
50μl|100μl|150μl
发货周期：
1～3天
产品价格：
询价
| 抗体名称 | Anti-MFAP1 Antibody |
| 指标别名 | MFAP1;AMP |
| 克隆性 | Polyclonal |
| 检验物种 | human |
| 应用范围 | WB,ICC/IF,FCM(Intracellular),ELISA |
| 基因名称 | MFAP1 |
| 抗体来源 | Rabbit |
| 抗体类型 | IgG |
| 免疫原 | E.coli-derived human MFAP1 recombinant protein (Position:D83-K437). |
| 成分 | 500μg/mL antibody with PBS，0.02% NaN3,1mg BSA and 50% glycerol. |
| 纯化方式 | Immunogen affinity purified. |
| 浓度 | 500μg/mL |
| 产品形态 | 溶液 |
| 保存条件 | 12 months from date of receipt，-20℃ as supplied.6 months 2 to 8℃ after reconstitution.Avoid repeated freezing and thawing. |
| 背景资料 | Microfibrillar-associated protein 1 is a protein that in humans is encoded by the MFAP1 gene.Microfibrils are an important component of the extracellular matrix of many tissues and can either associate with or without elastin.Several microfibril associated proteins (MFAPs) have been cloned,including MFAP1,MFAP3 and MFAP4.The MFAP1 and MFAP3 genes are localized near the fibrillin genes FBN1 and FBN2,respectively.Mutations in FBN1 are linked to Marfan syndrome.Mutations in FBN2 have been linked to congenital contractural arachnodactyly.This suggests roles for MFAP1 and MFAP3 in heritable diseases affecting microfibrils.Deletion of MFAP4 was found in 30 of 31 patients with Smith-Magenis syndrome (SMS),a clinically recognizable multiple congenital anomaly/mental retardation syndrome |
| Uniprot ID | P55081 |
| 推荐配套试剂 | Biorab recommends Enhanced Chemiluminescent Kit with anti-Rabbit IgG (ZN1926) for Western blot,and HRP Conjugated anti-Rabbit IgG Super Vision Assay Kit (ZN1865) for ICC. |
| 基因名全称 | microfibril associated protein 1 |
| 蛋白名全称 | Microfibrillar-associated protein 1 |
| 推荐稀释比 | Western blot (WB) 1:500～2000 Immunocytochemistry/Immunofluorescence (ICC/IF) 1:50～400 Flow Cytometry(Intracellular) 1～3μg/1×106 cells Enzyme linked immunosorbent assay (ELISA) 1:100～1000 |
| Gene ID | 79847 |
相关搜索：MFAP1抗体，MFAP1多抗，Anti-MFAP1 Antibody