
产品货号:
Z37408
中文名称:
IDS抗体
英文名称:
Anti-IDS Antibody (Clone#OTI1D9)
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 (Clone#OTI1D9) |
指标别名 | iduronate 2-sulfatase;ID2S;MPS2;SIDS |
克隆性 | Monoclonal |
检验物种 | human,mouse |
应用范围 | WB,IHC,IF,FCM |
基因名称 | IDS |
克隆号 | OTI1D9 |
抗体来源 | Mouse |
抗体类型 | IgG2a |
免疫原 | Full length human recombinant protein of human IDS(NP_000193) produced in HEK293T cell. |
实际分子量 | 59.2KD |
成分 | PBS (PH 7.3) containing 1% BSA,50% glycerol and 0.02% sodium azide. |
纯化方式 | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
浓度 | 500μg/mL |
产品形态 | 溶液 |
保存条件 | Stable for 12 months from date of receipt.Store at -20℃ as received. |
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 |
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 Immunohistochemistry in paraffin section (IHC) 1:150 Immunofluorescence (IF) 1:100 Flow cytometry (FCM) 1:100 |
相关搜索:IDS抗体,IDS单抗,Anti-IDS Antibody (Clone#OTI1D9)