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  2. 蛋白
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  4. Recombinant Human Iduronate 2-sulfatase (IDS)

Recombinant Human Iduronate 2-sulfatase (IDS)

  • 中文名稱：
    人IDS重組蛋白
  • 貨號(hào)：
    CSB-YP010998HU
  • 規(guī)格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    人IDS重組蛋白
  • 貨號(hào)：
    CSB-EP010998HU
  • 規(guī)格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    人IDS重組蛋白
  • 貨號(hào)：
    CSB-EP010998HU-B
  • 規(guī)格：
  • 來源：
    E.coli
  • 共軛：
    Avi-tag Biotinylated

    E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.

  • 其他：
  • 中文名稱：
    人IDS重組蛋白
  • 貨號(hào)：
    CSB-BP010998HU
  • 規(guī)格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    人IDS重組蛋白
  • 貨號(hào)：
    CSB-MP010998HU
  • 規(guī)格：
  • 來源：
    Mammalian cell
  • 其他：

產(chǎn)品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
  • Uniprot No.：
  • 別名：
    Alpha L iduronate sulfate sulfatase; Alpha-L-iduronate sulfate sulfatase; AW214631; Ids; IDS_HUMAN; Iduronate 2 sulfatase 14 kDa chain; Iduronate 2 sulfatase 42 kDa chain; Iduronate 2 sulfatase; Iduronate 2-sulfatase 14 kDa chain; Iduronate sulfatase; Idursulfase; MPS2; RP23-29M4.1; SIDS
  • 種屬：
    Homo sapiens (Human)
  • 蛋白長(zhǎng)度：
    Full Length of Mature Protein
  • 表達(dá)區(qū)域：
    34-455
  • 氨基酸序列
    TDALNVL LIIVDDLRPS LGCYGDKLVR SPNIDQLASH SLLFQNAFAQ QAVCAPSRVS FLTGRRPDTT RLYDFNSYWR VHAGNFSTIP QYFKENGYVT MSVGKVFHPG ISSNHTDDSP YSWSFPPYHP SSEKYENTKT CRGPDGELHA NLLCPVDVLD VPEGTLPDKQ STEQAIQLLE KMKTSASPFF LAVGYHKPHI PFRYPKEFQK LYPLENITLA PDPEVPDGLP PVAYNPWMDI RQREDVQALN ISVPYGPIPV DFQRKIRQSY FASVSYLDTQ VGRLLSALDD LQLANSTIIA FTSDHGWALG EHGEWAKYSN FDVATHVPLI FYVPGRTASL PEAGEKLFPY LDPFDSASQL MEPGRQSMDL VELVSLFPTL AGLAGLQVPP RCPVPSFHVE LCREGKNLLK HFRFRDLEED PYLPG
  • 蛋白標(biāo)簽：
    Tag?type?will?be?determined?during?the?manufacturing?process.
    The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
  • 產(chǎn)品提供形式：
    Lyophilized powder
    Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
  • 復(fù)溶：
    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
  • 儲(chǔ)存條件：
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質(zhì)期：
    The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
    Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
  • 貨期：
    Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
    Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
  • 注意事項(xiàng)：
    Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
  • Datasheet ：
    Please contact us to get it.

產(chǎn)品評(píng)價(jià)

相關(guān)產(chǎn)品

靶點(diǎn)詳情

  • 功能：
    Lysosomal enzyme involved in the degradation pathway of dermatan sulfate and heparan sulfate.
  • 基因功能參考文獻(xiàn)：
    1. 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
    2. 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
    3. 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
    4. 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
    5. A splicing mutation, c.709-1G>A, was detected in the proband, for which his mother was heterozygous. PMID: 28186595
    6. Extensive iduronate 2-sulfatase (Hunter syndrome) (IDS) gene deletions were identified in four mucopolysaccharidosis type II (MPSII) patients. PMID: 26762690
    7. 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
    8. p.Ser142Phe and p.Ile360Tyrfs*31 mutations caused the severe disease manifestation PMID: 24780617
    9. 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
    10. 30 novel iduronate sulfatase mutations have been identified in mucopolysaccharidosis type II Latin American patients. PMID: 24125893
    11. Identification of a splice site mutation in the IDS gene associated with mucopolysaccharidosis type II. PMID: 23867855
    12. 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
    13. A report of a novel IDS nonsense mutation resulting in mucopolysaccharidosis type II in several patients from a Chinese family. PMID: 22622771
    14. genetically analyze patients with severe Hunter syndrome that showed a total deletion of the iduronate-2-sulphatase (IDS) gene PMID: 22492741
    15. Family members with 3 generations of X-inactivation with Hunter syndrome have 1568A>G missence mutation in the IDS gene PMID: 21062272
    16. LCR-initiated rearrangements at the IDS locus, completed with Alu-mediated recombination or non-homologous end joining PMID: 21593745
    17. Hunter syndrome in Thailand is caused by a diverse set of defects affecting both IDS protein production and activity. PMID: 18500569
    18. 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
    19. 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
    20. 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
    21. patterns of cytosine methylation in the entire IDS gene PMID: 15146464
    22. 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
    23. a total of 17 identified missense, small deletion, and nonsense mutations were further characterized by transient expression studies. PMID: 15614569
    24. large deletion correlated with the severe phenotype of this Hunter syndrome patient. PMID: 15909065
    25. The IDS gene was analyzed in Japanese patients with mucopolysaccharidosis II. PMID: 16133661
    26. IDS activity in female carriers was less than a half of the normal level PMID: 16480701
    27. 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
    28. The balance between constitutive and cryptic splice sites in the IDS gene is very sensitive. PMID: 16699754
    29. A new point mutation (T1140C) in exon 8 of the IDS gene was found in Hunter syndrome. PMID: 16735228
    30. the IDS gene is prone to splicing mutations in Portuguese patients with mucopolysaccharidosis type II PMID: 17063374
    31. analysis of iduronate-2-sulfatase enzymatic activity, protein processing and structure PMID: 17091340
    32. 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
    33. Identification of a novel nonsense mutation (p.Y54X) in the IDS gene of severely affected MPS II patients of African origin. PMID: 17616540
    34. 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
    35. frame-shift deletion mutation (1062 del 16) was identified in exon 7 of the patient's IDS gene PMID: 17657858
    36. 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
    37. 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
    38. novel mutations in Italian patients with mucopolysaccharidosis type II PMID: 11462244

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  • 相關(guān)疾病：
    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：

    HGNC: 5389

    OMIM: 300823

    KEGG: hsa:3423

    STRING: 9606.ENSP00000339801

    UniGene: Hs.460960



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