Human iduronate sulfatase,IDS ELISA Kit
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中文名稱:人艾杜糖硫酸酯酶(IDS)酶聯(lián)免疫試劑盒
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貨號:CSB-E09471h
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規(guī)格:96T/48T
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價格:¥3600/¥2500
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其他:
產(chǎn)品詳情
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產(chǎn)品描述:人艾杜糖硫酸酯酶(IDS)酶聯(lián)免疫試劑盒(CSB-E09471h)為雙抗夾心法ELISA試劑盒,定量檢測血清、血漿、組織勻漿、細(xì)胞裂解物樣本中的IDS含量。人艾杜糖硫酸酯酶(IDS)是一種溶酶體酶,參與硫酸皮膚素和硫酸乙酰肝素的降解,其活性對于防止這些物質(zhì)在溶酶體內(nèi)積聚至關(guān)重要。IDS缺乏會導(dǎo)致亨特綜合征等溶酶體貯積癥,通過基因治療或酶替代療法來提高IDS活性是治療這些疾病的關(guān)鍵。試劑盒檢測范圍為31.25 pg/mL-2000 pg/mL,該產(chǎn)品廣泛應(yīng)用于代謝調(diào)控機(jī)制研究、溶酶體貯積癥疾病模型構(gòu)建、基因治療藥物效價評估等科研領(lǐng)域,實驗數(shù)據(jù)穩(wěn)定可靠,支持多樣本類型的重復(fù)檢測,為探索IDS相關(guān)分子通路及病理機(jī)制提供高效工具。本品僅用于科研,不用于臨床診斷,產(chǎn)品具體參數(shù)及操作步驟詳見產(chǎn)品說明書。
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別名:Alpha L iduronate sulfate sulfatase ELISA Kit; Alpha-L-iduronate sulfate sulfatase ELISA Kit; AW214631 ELISA Kit; Ids ELISA Kit; IDS_HUMAN ELISA Kit; Iduronate 2 sulfatase 14 kDa chain ELISA Kit; Iduronate 2 sulfatase 42 kDa chain ELISA Kit; Iduronate 2 sulfatase ELISA Kit; Iduronate 2-sulfatase 14 kDa chain ELISA Kit; Iduronate sulfatase ELISA Kit; Idursulfase ELISA Kit; MPS2 ELISA Kit; RP23-29M4.1 ELISA Kit; SIDS ELISA Kit
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縮寫:
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Uniprot No.:
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種屬:Homo sapiens (Human)
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樣本類型:serum, plasma, tissue homogenates, cell lysates
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檢測范圍:31.25 pg/mL-2000 pg/mL
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靈敏度:7.81 pg/mL
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反應(yīng)時間:1-5h
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樣本體積:50-100ul
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檢測波長:450 nm
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研究領(lǐng)域:Tags & Cell Markers
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測定原理:quantitative
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測定方法:Sandwich
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精密度:
Intra-assay Precision (Precision within an assay): CV%<8% Three samples of known concentration were tested twenty times on one plate to assess. Inter-assay Precision (Precision between assays): CV%<10% Three samples of known concentration were tested in twenty assays to assess. -
線性度:
To assess the linearity of the assay, samples were spiked with high concentrations of human IDS in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay. Sample Serum(n=4) 1:1 Average % 92 Range % 87-95 1:2 Average % 89 Range % 85-94 1:4 Average % 95 Range % 89-99 1:8 Average % 102 Range % 98-105 -
回收率:
The recovery of human IDS spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section. Sample Type Average % Recovery Range Serum (n=5) 96 93-102 EDTA plasma (n=4) 87 80-92 -
標(biāo)準(zhǔn)曲線:
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. pg/ml OD1 OD2 Average Corrected 2000 2.257 2.357 2.307 2.201 1000 1.976 1.872 1.924 1.818 500 1.532 1.578 1.555 1.449 250 1.172 1.151 1.162 1.056 125 0.711 0.728 0.720 0.614 62.5 0.426 0.434 0.430 0.324 31.25 0.262 0.270 0.266 0.160 0 0.105 0.106 0.106 -
數(shù)據(jù)處理:
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貨期:3-5 working days
相關(guān)產(chǎn)品
靶點(diǎn)詳情
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功能:Lysosomal enzyme involved in the degradation pathway of dermatan sulfate and heparan sulfate.
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基因功能參考文獻(xiàn):
- IDS structure revealed by X-ray crystallography provides essential insight into multiple mechanisms by which pathogenic mutations interfere with enzyme function, and a compelling explanation for severe Hunter syndrome phenotypes. PMID: 28593992
- Study analyzed the genotype-phenotype relationship for 17 patients with mucopolysaccharidosis II and performed expression studies for 12 variants, nine of which have not been reported previously; speculated that very low or cell-type-specific IDS residual activity is sufficient to prevent the neuronal phenotype. PMID: 28543354
- Study identified 16 novel mutations in the IDS gene and revealed that the severe type of mucopolysaccharidosis type II is strongly associated with large structural alteration of the gene. PMID: 27246110
- Functional characterization of all the novel sequence variants identified in the study would be helpful to confirm the clinical significance and to determine the effect of these variations on the function of respective proteins (IDUA and IDS) PMID: 27146977
- A splicing mutation, c.709-1G>A, was detected in the proband, for which his mother was heterozygous. PMID: 28186595
- Extensive iduronate 2-sulfatase (Hunter syndrome) (IDS) gene deletions were identified in four mucopolysaccharidosis type II (MPSII) patients. PMID: 26762690
- Two new mutations were discovered: p.K236N (c.708G>C) and p.Q80K (c.238C>A) which resulted in a severe phenotype and early death of Muccopolysaccharridosis Type II patients from Bulgaria and Macedonia. PMID: 22286622
- p.Ser142Phe and p.Ile360Tyrfs*31 mutations caused the severe disease manifestation PMID: 24780617
- This study evaluated a novel mutation in the IDS gene among 8 male Hunter syndrome patients; there was a quantitative deficiency of NK and B cell with normal responses in other immune parameters. PMID: 25038527
- 30 novel iduronate sulfatase mutations have been identified in mucopolysaccharidosis type II Latin American patients. PMID: 24125893
- Identification of a splice site mutation in the IDS gene associated with mucopolysaccharidosis type II. PMID: 23867855
- a novel (p.R468P) and five known (p.R88C, p.D148V, p.G224A, p.Y348X, and p.R468Q) IDS mutations were shown to result in proteins with little or no IDS activity and altered protein processing, when expressed in COS7 cells PMID: 22990955
- A report of a novel IDS nonsense mutation resulting in mucopolysaccharidosis type II in several patients from a Chinese family. PMID: 22622771
- genetically analyze patients with severe Hunter syndrome that showed a total deletion of the iduronate-2-sulphatase (IDS) gene PMID: 22492741
- Family members with 3 generations of X-inactivation with Hunter syndrome have 1568A>G missence mutation in the IDS gene PMID: 21062272
- LCR-initiated rearrangements at the IDS locus, completed with Alu-mediated recombination or non-homologous end joining PMID: 21593745
- Hunter syndrome in Thailand is caused by a diverse set of defects affecting both IDS protein production and activity. PMID: 18500569
- study describes a woman with mild manifestations of Hunter syndrome who gave birth to a daughter; both the mother and daughter carried the p.R443X mutation in exon 9 of the ID2S gene PMID: 21108396
- The in vivo correction of heritable gene lesions at the RNA level operating via a correction mechanism akin to RNA-editing, was observed for IDS mutant transcript. PMID: 20104590
- The results illustrated that the deletion and frame-shift mutation of c.876-877 del TC detected in IDS gene was a novel pathologic mutation,, which was the underlying cause of MPS II of this patient. PMID: 19933090
- patterns of cytosine methylation in the entire IDS gene PMID: 15146464
- Mucopolysaccharidosis type II patients with sever CNS involvement and age of onset by 3 years of age had four IDS amino acid substitutions S333L,C53X,E341K, and P480R. PMID: 15500445
- a total of 17 identified missense, small deletion, and nonsense mutations were further characterized by transient expression studies. PMID: 15614569
- large deletion correlated with the severe phenotype of this Hunter syndrome patient. PMID: 15909065
- The IDS gene was analyzed in Japanese patients with mucopolysaccharidosis II. PMID: 16133661
- IDS activity in female carriers was less than a half of the normal level PMID: 16480701
- These findings suggest methylation patterns in the beginning of IDS genomic region are polymorphic in humans and that hypermethylation in this region in some individuals predisposes them to CpG mutations resulting in Hunter syndrome. PMID: 16617305
- The balance between constitutive and cryptic splice sites in the IDS gene is very sensitive. PMID: 16699754
- A new point mutation (T1140C) in exon 8 of the IDS gene was found in Hunter syndrome. PMID: 16735228
- the IDS gene is prone to splicing mutations in Portuguese patients with mucopolysaccharidosis type II PMID: 17063374
- analysis of iduronate-2-sulfatase enzymatic activity, protein processing and structure PMID: 17091340
- Two novel mutations were identified in the human iduronate-2-sulfatase (IDS) gene in two patients from unrelated families with mucopolysaccharidosis type II(MPS II). PMID: 17284421
- Identification of a novel nonsense mutation (p.Y54X) in the IDS gene of severely affected MPS II patients of African origin. PMID: 17616540
- The molecular characterization of one novel missense mutation (p.S305P) and 1 splice site mutation (c.1006 +5G > C) associated with mucopolysaccharidosis type II was presented. PMID: 17655837
- frame-shift deletion mutation (1062 del 16) was identified in exon 7 of the patient's IDS gene PMID: 17657858
- A new mutation, an A>T change at nucleotide 595, substitutes a premature stop codon for a lysine at amino acid 199 of the IDS enzyme. PMID: 18546295
- IDS has a role in glucose-stimulated insulin secretion via a mechanism that involves the activation of exocytosis through phosphorylation of PKCalpha and MARCKS. PMID: 19602578
- novel mutations in Italian patients with mucopolysaccharidosis type II PMID: 11462244
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相關(guān)疾?。?/div>Mucopolysaccharidosis 2 (MPS2)亞細(xì)胞定位:Lysosome.蛋白家族:Sulfatase family組織特異性:Liver, kidney, lung, and placenta.數(shù)據(jù)庫鏈接:
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