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  4. Recombinant Human Xylosyltransferase 1 (XYLT1), partial

Recombinant Human Xylosyltransferase 1 (XYLT1), partial

  • 中文名稱：
    人XYLT1重組蛋白
  • 貨號：
    CSB-YP773057HU
  • 說明書：
  • 規格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    人XYLT1重組蛋白
  • 貨號：
    CSB-EP773057HU
  • 說明書：
  • 規格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    人XYLT1重組蛋白
  • 貨號：
    CSB-EP773057HU-B
  • 說明書：
  • 規格：
  • 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XYLT1重組蛋白
  • 貨號：
    CSB-BP773057HU
  • 說明書：
  • 規格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    人XYLT1重組蛋白
  • 貨號：
    CSB-MP773057HU
  • 說明書：
  • 規格：
  • 來源：
    Mammalian cell
  • 其他：

產品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
    XYLT1
  • Uniprot No.：
  • 別名：
    Beta D xylosyltransferase 1; O xylosyltransferase 1; Peptide O-xylosyltransferase 1; PXYLT1; UDP-D-xylose:proteoglycan core protein; XT-I; XT1; XTI; Xylosyltransferase 1; Xylosyltransferase I; xylosyltransferase iota; XylT-I; XYLT1; XYLT1_HUMAN
  • 種屬：
    Homo sapiens (Human)
  • 蛋白長度：
    Partial
  • 蛋白標簽：
    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.
  • 產品提供形式：
    Lyophilized powder Warning: in_array() expects parameter 2 to be array, null given in /www/web/cusabio_cn/public_html/caches/caches_template/default/content/show_product_protein.php on line 662
    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.
  • 儲存條件：
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質期：
    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：
    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.

產品評價

靶點詳情

  • 功能：
    Catalyzes the first step in the biosynthesis of chondroitin sulfate and dermatan sulfate proteoglycans, such as DCN. Transfers D-xylose from UDP-D-xylose to specific serine residues of the core protein. Required for normal embryonic and postnatal skeleton development, especially of the long bones. Required for normal maturation of chondrocytes during bone development, and normal onset of ossification.
  • 基因功能參考文獻：
    1. In conclusion, we identified two genes, DZIP1 and XYLT1, potentially associated with nonsyndromic high myopia using whole exome sequencing and subsequent mutation screening analysis. PMID: 28085539
    2. Novel and recurrent XYLT1 mutations in two Turkish families with Desbuquois dysplasia, type 2, have been reported. PMID: 27881841
    3. Our study describes the first case of DBQD2 resulting from compound heterozygous XYLT1 mutation, expands the mutational spectrum of the disease and provides evidence that the severe growth retardation and microsomia observed in DBQD2 patients may result not only from the skeletal dysplasia itself but also from GH and IGF-1 deficiency. PMID: 27030147
    4. XYLT1 mutation is associated with short limb skeletal dysplasia. PMID: 26601923
    5. Human XYLT1 promoter sequence analysis and description. PMID: 25480529
    6. These results suggest that XT-1 expression is refractory to the disease process and to inhibition by inflammatory cytokines and that signaling through AP-1, Sp1, and Sp3 is important in the maintenance of XT-1 levels in NP cells. PMID: 25476526
    7. five distinct homozygous XYLT1 mutations may have a role in Desbuquois dysplasia type 2 PMID: 24581741
    8. A family study shows that functional alterations of XYLT1 cause an autosomal recessive short stature syndrome associated with intellectual disability. PMID: 23982343
    9. XYLT1 activity increased time-dependently in response to progressive myofibroblast transformation. PMID: 23747722
    10. AP-1 and Sp3 are key regulators of IL-1beta-mediated modulation of xylosyltransferase I expression. PMID: 23223231
    11. Xylosyltransferase-I regulates glycosaminoglycan synthesis during the pathogenic process of human osteoarthritis PMID: 22479506
    12. DXD motifs in human xylosyltransferase I are required for enzyme activity PMID: 15294915
    13. Elevated XYLT1 activities in pseudoxanthoma elasticum patients is a marker of proteoglycan biosynthesis. PMID: 16133423
    14. xylotransferase genes might be potential candidate genes predisposing to diabetic nephropathy in type 1 diabetic patients PMID: 16164625
    15. Over 80% of the nucleotide sequence of the XT-I-cDNA is necessary for expressing a recombinant enzyme with full catalytic activity. PMID: 16225459
    16. recombinant expression and cloning of active full-length xylosyltransferase I (XT-I) and characterization of subcellular localization of XT-I and XT-II PMID: 16569644
    17. Variations in the XYLT-II gene are genetic co-factors in the severity of PXE. PMID: 16571645
    18. Increased levels of xylosyltransferase I correlates with the formation of extracellular matrix during chondrogenic differentiation of mesenchymal stem cells. PMID: 16778156
    19. The XYLT-I c.343G>T polymorphism contributes to the genetic susceptibility to development of diabetic nephropathy in type 1 diabetic patients. PMID: 17003309
    20. TGF-beta(1) and mechanical stress induce xylosyltransferase I expression in cardiac fibroblasts and have impact for ECM remodeling in the dilated heart. PMID: 17635914
    21. For the rate-limiting enzyme in glycosaminoglycan synthesis XT-I, maximal mRNA expression and enzyme activity were observed 10 days after osteogenic induction of mesenchymal stem cells, simultaneously to the beginning of ECM mineralization. PMID: 17980567
    22. results show that XT-I polymorphisms potentially confer to the genetic susceptibility of abdominal aortic aneurysm PMID: 18294457
    23. These results point to skeletal growth and tissue remodeling as a cause of the high XT activity in children PMID: 18763033
    24. Data show that the xylosyltransferase I SNP is associated with a decreased glycosaminoglycan amount in the serum of healthy blood donors. PMID: 19014925
    25. No statistically significant association was found between four XYLT variants and hypertension or blood pressure, suggesting that they do not play a significant role in the development of essential hypertension. PMID: 19197251
    26. AP-1 Sp1 family of transcription factors are necessary for the transcriptional regulation of the XYLT1 gene. PMID: 19762916

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  • 相關疾病：
    Desbuquois dysplasia 2 (DBQD2); Pseudoxanthoma elasticum (PXE)
  • 亞細胞定位：
    Golgi apparatus membrane; Single-pass type II membrane protein. Secreted.
  • 蛋白家族：
    Glycosyltransferase 14 family, XylT subfamily
  • 組織特異性：
    Widely expressed. Expressed at higher level in placenta, kidney and pancreas. Weakly expressed in skeletal muscle.
  • 數據庫鏈接：

    HGNC: 15516

    OMIM: 264800

    KEGG: hsa:64131

    STRING: 9606.ENSP00000261381

    UniGene: Hs.22907



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