Warning: mkdir(): No space left on device in /www/wwwroot/zhenghe1718.com/func.php on line 127

Warning: file_put_contents(./cachefile_yuan/99dujia.com/cache/75/37a72/60619.html): failed to open stream: No such file or directory in /www/wwwroot/zhenghe1718.com/func.php on line 115
Anti-PTPN11 Antibody |产品详情|进口榴莲视频免费观看采购网





    榴莲视频下载地址入口,8008APP幸福宝榴莲,榴莲视频免费观看,榴莲视频污污污下载

    订购信息
    上海榴莲视频下载地址入口生物科技公司
    Tel:400-968-7988    021-33779008
    Anti-PTPN11 Antibody
    品牌:Antibodies
    货号:
    规格:50µl
    货期:

    Anti-PTPN11 Antibody

    商品详情 参考文献 相关资料
    Name: Anti-PTPN11 Antibody
    See all PTPN11 primary antibodies
    Description: Rabbit polyclonal antibody to PTPN11.
    Applications: WB, IHC
    Dilutions: WB: 1:500 - 1:1000, IHC: 1:50 - 1:100.
    Reactivity: Human, Mouse, Rat
    Immunogen: Recombinant protein of human PTPN11.
    Protein Length: 593
    Host: Rabbit
    Clonality: Polyclonal
    Isotype: IgG
    Conjugate: Unconjugated
    Purification: Affinity purification.
    Product Form: Liquid
    Formulation: Supplied in Phosphate Buffered Saline, pH 7.30, with 0.02% Sodium Azide and 50% Glycerol.
    Storage: Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
    Function: Acts downstream of various receptor and cytoplasmic protein tyrosine kinases to participate in the signal transduction from the cell surface to the nucleus. Dephosphorylates ROCK2 at Tyr-722 resulting in stimulatation of its RhoA binding activity. Dephosphorylates CDC73 (PubMed:26742426).
    Tissue Specificity: Widely expressed, with highest levels in heart, brain, and skeletal muscle.
    Involvement in Disease: LEOPARD syndrome 1: A disorder characterized by lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormalities of genitalia, retardation of growth, and sensorineural deafness.

    Noonan syndrome 1: A form of Noonan syndrome, a disease characterized by short stature, facial dysmorphic features such as hypertelorism, a downward eyeslant and low-set posteriorly rotated ears, and a high incidence of congenital heart defects and hypertrophic cardiomyopathy. Other features can include a short neck with webbing or redundancy of skin, deafness, motor delay, variable intellectual deficits, multiple skeletal defects, cryptorchidism, and bleeding diathesis. Individuals with Noonan syndrome are at risk of juvenile myelomonocytic leukemia, a myeloproliferative disorder characterized by excessive production of myelomonocytic cells. Some patients with NS1 develop multiple giant cell lesions of the jaw or other bony or soft tissues, which are classified as pigmented villonodular synovitis (PVNS) when occurring in the jaw or joints.

    Leukemia, juvenile myelomonocytic: An aggressive pediatric myelodysplastic syndrome/myeloproliferative disorder characterized by malignant transformation in the hematopoietic stem cell compartment with proliferation of differentiated progeny. Patients have splenomegaly, enlarged lymph nodes, rashes, and hemorrhages.

    Metachondromatosis: A skeletal disorder with radiologic features of both multiple exostoses and Ollier disease, characterized by the presence of exostoses, commonly of the bones of the hands and feet, and enchondromas of the metaphyses of long bones and iliac crest.
    Sequence Similarities: Belongs to the protein-tyrosine phosphatase family. Non-receptor class 2 subfamily.
    Post-Translational Modification: Phosphorylated on Tyr-546 and Tyr-584 upon receptor protein tyrosine kinase activation; which creates a for GRB2 and other SH2-containing proteins. Phosphorylated upon activation of the receptor-type kinase FLT3. Phosphorylated upon activation of the receptor-type kinase PDGFRA (By similarity). Phosphorylated by activated PDGFRB.
    Cellular locations: Cytoplasm. Nucleus.
    Database Links:
  1. Entrez Gene: 5781?Human
  2. Entrez Gene: 19247?Mouse
  3. Entrez Gene: 25622?Rat
  4. Omim: 176876?Human
  5. SwissProt: Q06124?Human
  6. SwissProt: P35235?Mouse
  7. SwissProt: P41499?Rat
  8. Unigene: 506852?Human
  9. Unigene: 474046?Mouse
  10. Unigene: 8681?Mouse
  11. Unigene: 98209?Rat
  12. Synonyms:
  13. BPTP3 Antibody
  14. CFC Antibody
  15. JMML Antibody
  16. METCDS Antibody
  17. MGC14433 Antibody
  18. NS1 Antibody
  19. OTTHUMP00000166107 Antibody
  20. OTTHUMP00000166108 Antibody
  21. Protein tyrosine phosphatase 2 Antibody
  22. Protein tyrosine phosphatase 2C Antibody
  23. Protein tyrosine phosphatase non receptor type 11 Antibody
  24. Protein-tyrosine phosphatase 1D Antibody
  25. Protein-tyrosine phosphatase 2C Antibody
  26. PTN11_HUMAN Antibody
  27. PTP-1D Antibody
  28. PTP-2C Antibody
  29. PTP1D Antibody
  30. PTP2C Antibody
  31. PTPN11 Antibody
  32. SAP2 Antibody
  33. SH-PTP2 Antibody
  34. SH-PTP3 Antibody
  35. SH2 domain containing protein tyrosine phosphatase 2 Antibody
  36. SHP 2 Antibody
  37. SHP-2 Antibody
  38. SHP2 Antibody
  39. SHPTP2 Antibody
  40. SHPTP3 Antibody
  41. Syp Antibody
  42. Tyrosine-protein phosphatase non-receptor type 11 Antibody
  43. Information: Target information shown above is from the UniProt Consortium.
    • 关于榴莲视频下载地址入口
    • 购物流程
    • 支付方式
    • 配送方式
    Copyright@ 2003-2026  进口榴莲视频免费观看采购网版权所有     

    BIOLEAF热搜   BIOLEAF8008APP幸福宝榴莲   BIOLEAF ELISA   BIOLEAF榴莲视频免费观看   BIOLEAF品牌   BIOLEAF抗体   BIOLEAF耗材   BIOLEAF小仪器

    sitemap   细胞库查询   危险品图标

    本公司网站所展示销售的产品仅供科研!

             沪ICP备08023583号-6     
    产品咨询
    QQ扫码沟通
    在线客服
    服务电话
    400-968-7988
    扫码关注
    微信公众号二维码

    沪公网安备 31011202007338号

    网站地图