产品货号：
Z18697
中文名称：
IDS抗体
英文名称：
Anti-IDS 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-IDS Antibody |
| 指标别名 | iduronate 2-sulfatase;ID2S;MPS2;SIDS |
| 克隆性 | Polyclonal |
| 检验物种 | human |
| 应用范围 | WB |
| 基因名称 | IDS |
| 抗体来源 | Rabbit |
| 抗体类型 | IgG |
| 免疫原 | A synthetic peptide corresponding to a sequence at the C-terminus of human Iduronate 2 sulfatase(430-448aa ELCREGKNLLKHFRFRDLE). |
| 实际分子量 | 62KD |
| 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 | IDS(Iduronate-2-sulfatase) is a sulfatase enzyme associated with Hunter syndrome.Iduronate 2-sulfatase is involved in the lysosomal degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate.Wilson et al.(1991) used an IDS cDNA clone to localize the gene to Xq28,distal to the fragile X site.Faust et al.(1992) and Daniele et al.(1993) demonstrated that the homologous Ids gene in the mouse occupies the same position on the X chromosome in relation to the FMR1,F9,and GABRA3 genes.Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate.Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked mucopolysaccharidosis type II,also known as Hunter syndrome.Iduronate-2-sulfatase has a strong sequence homology with human arylsulfatases A,B,and C,and human glucosamine-6-sulfatase. |
| Uniprot ID | P22304 |
| 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 IHC(P).*Blocking peptide可以联系我们购买。 |
| 基因名全称 | iduronate 2-sulfatase |
| 蛋白名全称 | Iduronate 2-sulfatase |
| 推荐稀释比 | Western blot(WB) 1:500～2000 |
相关搜索：IDS抗体，IDS多抗，Anti-IDS Antibody