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PHEX Antibody, HRP conjugated

  • 中文名稱：
    PHEX兔多克隆抗體, HRP偶聯(lián)
  • 貨號：
    CSB-PA017896LB01HU
  • 規(guī)格：
    ￥880
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱：
    Rabbit anti-Homo sapiens (Human) PHEX Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    PHEX
  • 別名：
    PHEX; PEX; Phosphate-regulating neutral endopeptidase PHEX; Metalloendopeptidase homolog PEX; Vitamin D-resistant hypophosphatemic rickets protein; X-linked hypophosphatemia protein; HYP
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human
  • 免疫原：
    Recombinant Human Phosphate-regulating neutral endopeptidase protein (524-673AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標(biāo)記方式：
    HRP
  • 克隆類型：
    Polyclonal
  • 抗體亞型：
    IgG
  • 純化方式：
    >95%, Protein G purified
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA
  • Protocols：
  • 儲存條件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

產(chǎn)品評價

靶點詳情

  • 功能：
    Peptidase that cleaves SIBLING (small integrin-binding ligand, N-linked glycoprotein)-derived ASARM peptides, thus regulating their biological activity. Cleaves ASARM peptides between Ser and Glu or Asp residues. Regulates osteogenic cell differentiation and bone mineralization through the cleavage of the MEPE-derived ASARM peptide. Promotes dentin mineralization and renal phosphate reabsorption by cleaving DMP1- and MEPE-derived ASARM peptides. Inhibits the cleavage of MEPE by CTSB/cathepsin B thus preventing MEPE degradation.
  • 基因功能參考文獻(xiàn)：
    1. Nonsense mutation (p.E145*) in PHEX is involved in X-linked dominant hypophosphatemic rickets. PMID: 29858904
    2. Two novel variants of the PHEX gene were identified in two unrelated families with Xlinked dominant hypophosphatemic rickets by directly sequencing all 22 exon regions and intron/exon boundaries of the PHEX gene. PMID: 29393334
    3. genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3 PMID: 29505567
    4. PHEX mutations are still the most common genetic defects in the Turkish population and were found in 12 of 14 patients with hypophosphataemic rickets PMID: 28383812
    5. dentification of the PHEX mutation by whole exome sequencing has facilitated genetic counseling and prenatal diagnosis for the family affected with hypophosphatemic rickets PMID: 28981921
    6. Expression and inactivation of osteopontin-degrading PHEX enzyme in squamous cell carcinoma PMID: 27270332
    7. The novel splicing mutation IVS21+2T>G of the PHEX geneis associated with X-linked hypophosphatemia. PMID: 28397222
    8. c.931dupC and IVS14+1G>A are two novel mutations of the PHEX gene and might be the new pathogenic mutations of X-linked hypophosphatemic rickets PMID: 28506344
    9. Herpes simplex virus 1 blocks MAVS-Pex mediated early interferon-stimulated gene activation through VP16 to dampen the immediate early antiviral innate immunity signaling from peroxisomes. PMID: 28222744
    10. Mutation in the PHEX gene is associated with type 1 diabetes. PMID: 26894575
    11. the findings of this study provide new insight into the spectrum of PHEX mutations and provide potential evidence of a critical domain in PHEX protein. PMID: 27840894
    12. This report that mutations in PHEX are the most frequent cause of hypophosphatemic rickets PMID: 26051471
    13. Downregulation of PHEX may constitute an important early component of bone loss and joint damage in leprosy PMID: 26362198
    14. A new splice acceptor mutation was seen in intron 9 (c.1080-3C>A) in a family with hypophosphatemic rickets. This transcript skipped exons 10-14. A sporadic case had a new exon 11 mutation (c.1211_1215delACAAAinsTTTACAT, p.Asp404Valfs*5, de novo). PMID: 26107949
    15. Two novel mutations were detected unrelated families with hypophosphatemic rickets. PMID: 24836714
    16. PHEX c.*231A > G can masquerade as sporadic or X-linked recessive HR. PMID: 25042154
    17. A novel de novo nonsense mutation of the PHEX gene has been identified in Chinese family expanding the mutation spectrum of PHEX leading to X-linked hypophosphatemic rickets. PMID: 25839938
    18. exon 22 is the mutation hot spot and missense mutation is the most common type of mutation in the PHEX gene in Chinese X-link dominate hypophosphatemic rickets (XLH) patients PMID: 24857004
    19. 15 PHEX mutations have been reported in Chinese populations with X-linked hypophosphatemic rickets PMID: 23813354
    20. The c.732+1G>T mutation of PHEX is associated with hypophosphatasia pedigree. PMID: 24078575
    21. study shows that PHEX mutation is a common cause of either familial or sporadic hypophosphatemic rickets in Turkish population PMID: 23079138
    22. Mutations in PHEX and DMP1 play a role in causing hypophosphatemic rickets. PMID: 22695891
    23. PHEX gene mutations were responsible for X-linked hypophosphatemia in these Chinese families. PMID: 22713460
    24. Analysis of PHEX mRNA from peripheral blood would be appropriate for the first screening step in determining the etiology of FGF23-related hypophosphatemic rickets. PMID: 22577109
    25. PTHrP(1-34)-mediated repression of the PHEX gene in osteoblastic cells involves the transcriptional repressor E4BP4. PMID: 21826652
    26. Hypophosphatemic rickets (HR) is a rare hereditary disease in which dental problems in terms of spontaneous periapical infections are frequently reported PMID: 21902707
    27. tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type in X-linked dominant Hypophosphatemic Rickets PMID: 21902834
    28. Novel PHEX nonsense mutation in a patient with X-linked hypophosphatemic rickets and review of current therapeutic regimens. PMID: 21553362
    29. Three novel mutations in the PHEX gene in Chinese subjects with hypophosphatemic rickets extends genotypic variability. PMID: 21293852
    30. Data show the wide spectrum of genetic variation that can be seen in PHEX, FGF23 and DMP1 when screening a large cohort with hypophosphatemic rickets. PMID: 21050253
    31. M. leprae is capable of inhibiting PHEX expression in osteoblasts in a very similar manner as that observed in Schwann cells, indicating that the bacillus modulates PHEX in both osteogenic and non-osteogenic cells. PMID: 20835608
    32. Case Report: describe a novel nonsense mutation in exon 3 of the PHEX gene (Glu(96)X (c.286G>T) causing X linked hypophosphatemic rickets in a mother and daughter of Indian ancestry. PMID: 20664300
    33. Cooperative role of NF-{kappa}B and poly(ADP-ribose) polymerase 1 (PARP-1) in the TNF-induced inhibition of PHEX expression in osteoblasts. PMID: 20817730
    34. fibroblast growth factor-23 and matrix extracellular phosphoglycoprotein sequences are potential PHEX substrates PMID: 12678920
    35. There is evidence for a hormone/enzyme/extracellular matrix protein cascade involving fibroblastic growth factor 23 (FGF23), a phosphate-regulating gene with homologies to (PHEX) and (MEPE)--REVIEW PMID: 12791601
    36. regulates fgf23 expression as part of a potential hormonal axis between bone and kidney that controls systemic phosphate homeostasis and mineralization PMID: 12874285
    37. Anthropometric characteristics arising from mutations of PHEX were evaluated. PMID: 15057978
    38. a cis-element is required for PHEX gene transcription that participates in negative feedback control of PHEX expression and thereby modulates the actions of phosphatonin PMID: 15337762
    39. In our present study, we found that suppression of PHEX expression by PHEX antisense in human osteoblast cells caused an increase in cathepsin D expression at protein, but not mRNA, levels. PMID: 15896324
    40. Overexpression of human PHEX under the human beta-actin promoter in hypophosphatemia mice rescued the bone phenotype almost completely, but did not affect phosphate homeostasis. PMID: 15940367
    41. seven PHEX mutations were detected in X-linked hypophosphatemic rickets patients: two missense mutations, two nonsense mutations, and three short deletions; no functional FGF23 mutation was detected in any patient PMID: 16055933
    42. XLH is caused by mutations in the PHEX (phosphate regulating gene with homology to endopeptidases) gene, which is located on Xp22.1. PMID: 16437029
    43. Our data support previous findings and therefore contribute to the decipherment of the pathogenetic pathways of XLH. PMID: 17406123
    44. The results suggest that PHEX gene mutations were responsible for XLH in these patients and these mutations may contribute to a higher serum fibroblast growth factor 23 level. PMID: 18046499
    45. Skeletal disease tended to be more severe in the group with a mutation in the C-terminal half of the PHEX gene, but no genotype-phenotype correlation was detected in other comparisons. PMID: 18162710
    46. These data provide evidence that aberrant Phex function in osteoblasts and/or osteocytes alone is sufficient to underlie the hyp-mouse phenotype. PMID: 18172553
    47. mRNA of PHEX involved in the pathogenesis of hypophosphataemic rickets is highly expressed in cells of the osteoblasts/osteocyte lineage. PMID: 18214537
    48. Normal growth and muscle dysfunction in X-linked hypophosphatemic rickets associated with a novel mutation in the PHEX gene. PMID: 18252791
    49. U(2)OS cells transfected with wild-type TNAP and polymorphism TNAP cDNA showed PHEX (phosphate-regulating gene with homologies to endopeptidases on the X chromosome) induction as in SaOS-2 cells. PMID: 18455459
    50. Data indicate that there is no single predominant PHEX mutation responsible for X-linked hypophosphatemic rickets. PMID: 18625346

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  • 相關(guān)疾?。?/div>
    Hypophosphatemic rickets, X-linked dominant (XLHR)
  • 亞細(xì)胞定位：
    Cell membrane; Single-pass type II membrane protein.
  • 蛋白家族：
    Peptidase M13 family
  • 組織特異性：
    Specifically expressed in ovary. Expressed at low levels in kidney.
  • 數(shù)據(jù)庫鏈接：

    HGNC: 8918

    OMIM: 300550

    KEGG: hsa:5251

    STRING: 9606.ENSP00000368682

    UniGene: Hs.495834