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  4. Recombinant Human Receptor-type tyrosine-protein phosphatase delta (PTPRD), partial

Recombinant Human Receptor-type tyrosine-protein phosphatase delta (PTPRD), partial

  • 中文名稱：
    人PTPRD重組蛋白
  • 貨號：
    CSB-YP019051HU
  • 規(guī)格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    人PTPRD重組蛋白
  • 貨號：
    CSB-EP019051HU
  • 規(guī)格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    人PTPRD重組蛋白
  • 貨號：
    CSB-EP019051HU-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PTPRD重組蛋白
  • 貨號：
    CSB-BP019051HU
  • 規(guī)格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    人PTPRD重組蛋白
  • 貨號：
    CSB-MP019051HU
  • 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：
    PTPRD; Receptor-type tyrosine-protein phosphatase delta; Protein-tyrosine phosphatase delta; R-PTP-delta; EC 3.1.3.48
  • 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(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(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：
    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)品評價

靶點詳情

  • 功能：
    Can bidirectionally induce pre- and post-synaptic differentiation of neurons by mediating interaction with IL1RAP and IL1RAPL1 trans-synaptically. Involved in pre-synaptic differentiation through interaction with SLITRK2.
  • 基因功能參考文獻：
    1. PTPRD rs35929428 might play a role in hepatic lipid accumulation and fibrosis, followed by the development of NAFLD. PMID: 28497593
    2. Results show the existence of a perturbed PTPRD-STAT3 axis potentially driving malignant progression of Hepatitis C virus-associated liver disease. PMID: 28159835
    3. Presynaptic differentiation induced by protein tyrosine phosphatase receptor type D (PTPdelta)-leucine rich repeat and fibronectin type III domain containing 5 (SALM5) requires the dimeric property of SALM5. PMID: 29348429
    4. In the 2:2 heterotetrameric SALM5/PTPdelta complex, a SALM5 dimer bridges two separate PTPdelta molecules. PMID: 29348579
    5. our study suggested that PTPRD loci are candidate susceptibility regions that have some marker SNPs for GDM in Han Chinese PMID: 27738328
    6. We investigated the modification of air pollution and diabetes association by a genetic risk score covering 63 T2D genes. Five single variants near GRB14, UBE2E2, PTPRD, VPS26A and KCNQ1 showed nominally significant interactions with PM10 (P<0.05). Our results suggest that genetic risk for T2D may modify susceptibility to air pollution through alterations in insulin sensitivity PMID: 27281273
    7. Mutation in PTPRD gene is associated with nodal marginal zone lymphoma. PMID: 27335277
    8. Low PTPRD expression is associated with Head and Neck Squamous Cell Carcinoma. PMID: 27501229
    9. The data provide evidence of the high incidence of PTPRD inactivation in laryngeal squamous cell carcinoma, suggesting that deletions and loss-of-function mutations are responsible for PTPRD loss only in a fraction of cases, whereas DNA methylation is the dominating mechanism of PTPRD inactivation. PMID: 28345455
    10. PTPRD polymorphisms might modulate antipsychotic-induced weight gain. PMID: 26656879
    11. overexpression in acute myeloid leukaemia cells inhibited cell proliferation and clonogenicity as well as inducing apoptosis PMID: 26607758
    12. PTPRD was identified as a novel locus potentially associated with blood pressure response to atenolol and resistant hypertension in multiple ethnic groups. PMID: 26425837
    13. PTPRD mutation, but not methylation or copy number loss, may serve as a predictive biomarker of sensitivity to STAT3 inhibitors in HNSCC. PMID: 26267899
    14. Study shows for the first time that DNMT1 caused PTPRD DNA hypermethylation and induced insulin signaling silencing in T2D patients. PMID: 26079428
    15. PTPRD is homozygously deleted and epigenetically downregulated in hepatocellular carcinomas (HCCs). PMID: 25831062
    16. This study demonstrated that the copy number variations of PTPRD relate to opioid dependence. PMID: 25345593
    17. Silencing PTPRD expression by siRNA treatment significantly enhanced cell proliferation compared with mock siRNA treatment. PMID: 25412184
    18. we report desmoplakin, a desmosomal protein that is implicated in cell-cell adhesion, as a novel PTPRD substrate. PMID: 25113440
    19. Ptprd is a tumor suppressor that can promote tumorigenesis in concert with Cdkn2a loss. PMID: 25138050
    20. The absence of MIM led to PTPdelta-mediated activation of SRC. PMID: 25287652
    21. We reveal that PTPRD is a bona fide tumor suppressor, pinpoint PTPRD loss as a cause of aberrant STAT3 activation in gliomas, and establish PTPRD loss, in the setting of CDKN2A/p16(INK4A) deletion, as a driver of glioma progression. PMID: 24843164
    22. Data suggest that PTPRD germline mutations may play a role in the development of Ewing sarcoma. PMID: 23800680
    23. Data indicate that expression of several predicted chimeric genes and genes with disrupted exon structure including ALK, NBAS, FHIT, PTPRD and ODZ4 in neuroblastoma. PMID: 23991058
    24. Loss of PTPRD gene is associated with squamous cell carcinomas of the vulva. PMID: 23404381
    25. Polymorphism in protein tyrosine phosphatase receptor delta is associated with the risk of clear cell renal cell carcinoma. PMID: 23069849
    26. This is the first report to observe an association between deletion within PTPRD and metastatic cutaneous squamous cell carcinoma. PMID: 22052591
    27. Although endogenous PTPdelta expression was very low in neuroblastoma cells, it was also low in mouse embryo adrenal glands, suggesting that PTPdelta may have little developmental function in early adrenal neuroblasts. PMID: 22571343
    28. Data indicate that genetic variants near the KCNQ1 and MAF/WWOX genes are associated with reduced insulin secretion, and the PTPRD genetic variant appears to be associated with progression to diabetes in Han Chinese. PMID: 21767287
    29. PTPRD has a tumor suppressor function in neuroblastoma through AURKA dephosphorylation and destabilization and a downstream destabilization of MYCN protein, representing a novel mechanism for the function of PTPRD in neuroblastoma. PMID: 22305495
    30. The interaction of the IL1RAPL1 family of proteins with PTPdelta and RhoGAP2 reveals a pathophysiological mechanism of cognitive impairment associated with a novel type of trans-synaptic signaling. PMID: 21926414
    31. Eight suggestive significant loci were detected with a series of genes expressed within the inner ear that underlie the auditory function, such as: DCLK1, PTPRD, GRM8, CMIP. PMID: 21493956
    32. Both family-based and population-based association studies suggest that PTPRD variant rs1975197 confers risk of RLS. PMID: 21264940
    33. statistical significant downregulation of PCDH17/PCH68 and PTPRD was observed PMID: 21213369
    34. Results found the PTPRD gene was most frequently homozygously deleted gene in human lung cancer among genes mapping to regions other than 9p21. PMID: 20073072
    35. Trans-synaptic adhesions between netrin-G ligand-3 (NGL-3) and receptor tyrosine phosphatases LAR, protein-tyrosine phosphatase delta (PTPdelta), and PTPsigma via specific domains regulate excitatory synapse formation. PMID: 20139422
    36. A novel isoform of PTPRD was cloned and its expression analyzed. PMID: 16114034
    37. data identify PTPRD as a candidate tumor suppressor gene in cutaneous squamous cell carcinoma with a possible association with metastasis PMID: 17420988
    38. The aberrant splicing or microdeletion of 5' UTR exons in such a high proportion of tumors indicates that loss of these exons dys-regulates the mRNA sequence PMID: 18050303
    39. The results indicate that polymorphisms of PTPRD are strongly associated with pediatric bronchial asthma in the Taiwanese population. PMID: 18414509
    40. Two independent SNPs in the 5' UTR of splice variants expressed predominantly in the central nervous system showed highly significant P values, identifying PTPRD as the fourth genome-wide significant locus for restless legs syndrome. PMID: 18660810
    41. These results implicate PTPRD as a tumor suppressor on chromosome 9p that is involved in the development of glioblastoma multiforme and multiple human cancers. PMID: 19478061
    42. No mutations of PTPRD were associated with familiar melanoma PMID: 19500277
    43. Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study PMID: 19525478

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  • 亞細胞定位：
    Membrane; Single-pass type I membrane protein.
  • 蛋白家族：
    Protein-tyrosine phosphatase family, Receptor class 2A subfamily
  • 數(shù)據(jù)庫鏈接：

    HGNC: 9668

    OMIM: 601598

    KEGG: hsa:5789

    STRING: 9606.ENSP00000348812

    UniGene: Hs.446083