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 Anti-ATP6AP2 Antibody |产品详情|进口榴莲视频免费观看采购网





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    Anti-ATP6AP2 Antibody
    品牌:Antibodies
    货号:
    规格:50µl
    货期:

    Anti-ATP6AP2 Antibody

    商品详情 参考文献 相关资料
    Name: Anti-ATP6AP2 Antibody
    See all ATP6AP2 primary antibodies
    Description: Rabbit polyclonal antibody to ATP6AP2.
    Applications: WB, IHC, IF
    Dilutions: WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:100.
    Reactivity: Human
    Immunogen: Recombinant protein of human ATP6AP2.
    Protein Length: 350
    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: Functions as a renin and prorenin cellular receptor. May mediate renin-dependent cellular responses by activating ERK1 and ERK2. By increasing the catalytic efficiency of renin in AGT/angiotensinogen conversion to angiotensin I, it may also play a role in the renin-angiotensin system (RAS).
    Tissue Specificity: Expressed in brain, heart, placenta, liver, kidney and pancreas. Barely detectable in lung and skeletal muscles. In the kidney cortex it is restricted to the mesangium of glomeruli. In the coronary and kidney artery it is expressed in the subendothelium, associated to smooth muscles where it colocalizes with REN. Expressed in vascular structures and by syncytiotrophoblast cells in the mature fetal placenta.
    Involvement in Disease: Mental retardation, X-linked, with epilepsy: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRXE patients manifest mild to moderate mental retardation associated with epilepsy, delays in motor milestones and speech acquisition in infancy.

    Parkinsonism with spasticity, X-linked: A syndrome characterized by parkinsonian features, such as cogwheel rigidity, resting tremor and bradykinesia, and variably penetrant spasticity.
    Post-Translational Modification: Phosphorylated.
    Cellular locations: Membrane.
    Database Links:
  1. Entrez Gene: 10159?Human
  2. Omim: 300556?Human
  3. SwissProt: O75787?Human
  4. Unigene: 495960?Human
  5. Synonyms:
  6. APT6M8 9 Antibody
  7. APT6M8-9 Antibody
  8. ATP6AP2 Antibody
  9. ATP6IP2 Antibody
  10. ATP6M8-9 Antibody
  11. ATPase H(+)-transporting lysosomal accessory protein 2 Antibody
  12. ATPase H(+)-transporting lysosomal-interacting protein 2 Antibody
  13. ATPase H+ transporting lysosomal accessory protein 2 Antibody
  14. ATPase H+ transporting lysosomal interacting protein 2 Antibody
  15. ATPase H+ transporting lysosomal vacuolar proton pump membrane sector associated protein M8 9 Antibody
  16. ATPase membrane sector associated protein M8 9 Antibody
  17. ATPase, H+ transporting, lysosomal (vacuolar proton pump) membrane sector associated protein M8 9 Antibody
  18. CAPER Antibody
  19. ELDF10 Antibody
  20. Embryonic liver differentiation factor 10 Antibody
  21. ER localized type I transmembrane adaptor Antibody
  22. ER-localized type I transmembrane adaptor Antibody
  23. HT028 Antibody
  24. M8 9 Antibody
  25. M8-9 Antibody
  26. MGC99577 Antibody
  27. MRXE Antibody
  28. MSTP009 Antibody
  29. N14F Antibody
  30. Renin receptor Antibody
  31. Renin/prorenin receptor Antibody
  32. RENR_HUMAN Antibody
  33. V ATPase M8 9 subunit Antibody
  34. V ATPase M8.9 subunit Antibody
  35. V-ATPase M8.9 subunit Antibody
  36. Vacuolar ATP synthase membrane sector associated protein M8 9 Antibody
  37. Vacuolar ATP synthase membrane sector-associated protein M8-9 Antibody
  38. vacuolar proton ATP synthase membrane sector associated protein M8 9 Antibody
  39. XMRE Antibody
  40. Information: Target information shown above is from the UniProt Consortium.
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