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





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

    Anti-CTSA Antibody

    商品详情 参考文献 相关资料
    Name: Anti-CTSA Antibody
    See all CTSA primary antibodies
    Description: Rabbit polyclonal antibody to CTSA.
    Applications: WB, IF
    Dilutions: WB: 1:500 - 1:2000, IF: 1:20 - 1:50.
    Reactivity: Human, Mouse, Rat
    Immunogen: Recombinant protein of human CTSA.
    Protein Length: 480
    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: Protective protein appears to be essential for both the activity of beta-galactosidase and neuraminidase, it associates with these enzymes and exerts a protective function necessary for their stability and activity. This protein is also a carboxypeptidase and can deamidate tachykinins.
    Involvement in Disease: Galactosialidosis: A lysosomal storage disease associated with a combined deficiency of beta-galactosidase and neuraminidase, secondary to a defect in cathepsin A. All patients have clinical manifestations typical of a lysosomal disorder, such as coarse facies, cherry red spots, vertebral changes, foam cells in the bone marrow, and vacuolated lymphocytes. Three phenotypic subtypes are recognized. The early infantile form is associated with fetal hydrops, edema, ascites, visceromegaly, skeletal dysplasia, and early death. The late infantile type is characterized by hepatosplenomegaly, growth retardation, cardiac involvement, and a normal or mildly affected mental state. The juvenile/***** form is characterized by myoclonus, ataxia, angiokeratoma, mental retardation, neurologic deterioration, absence of visceromegaly, and long survival.
    Sequence Similarities: Belongs to the peptidase S10 family.
    Cellular locations: Lysosome.
    Database Links:
  1. Entrez Gene: 5476 Human
  2. Entrez Gene: 19025 Mouse
  3. Entrez Gene: 296370 Rat
  4. Omim: 613111 Human
  5. SwissProt: P10619 Human
  6. SwissProt: P16675 Mouse
  7. Unigene: 609336 Human
  8. Unigene: 359633 Mouse
  9. Unigene: 474586 Mouse
  10. Unigene: 104631 Rat
  11. Synonyms:
  12. beta galactosidase 2 Antibody
  13. BETA GALACTOSIDASE PROTECTIVE PROTEIN Antibody
  14. beta-galactosidase 2 Antibody
  15. beta-galactosidase protective protein Antibody
  16. betagalactosidase 2 Antibody
  17. Carboxypeptidase C Antibody
  18. Carboxypeptidase L Antibody
  19. carboxypeptidase Y-like kininase Antibody
  20. Cathepsin A Antibody
  21. Ctsa Antibody
  22. deamidase Antibody
  23. EC 3.4.16.5 Antibody
  24. Glactosialidosis Antibody
  25. GLB2 Antibody
  26. Goldberg Syndrome Antibody
  27. GSL Antibody
  28. lysosomal carboxypeptidase A Antibody
  29. Lysosomal protective protein Antibody
  30. Lysosomal protective protein 20 kDa chain Antibody
  31. Lysosomal protective protein deficiency Antibody
  32. NEURAMINIDASE BETA GALACTOSIDASE EXPRESSION; NGBE Antibody
  33. Neuraminidase deficiency with beta-galactosidase deficiency Antibody
  34. NGBE Antibody
  35. OTTHUMP00000031778 Antibody
  36. OTTHUMP00000031781 Antibody
  37. PPCA Antibody
  38. PPCA deficiency Antibody
  39. PPGB Antibody
  40. PPGB_HUMAN Antibody
  41. Protective protein cathepsin A Antibody
  42. Protective protein for beta galactosidase Antibody
  43. Protective protein for beta-galactosidase Antibody
  44. Protective protein/Cathepsin A (PPCA) Antibody
  45. Protective protein/cathepsin A deficiency Antibody
  46. urinary kininase Antibody
  47. Information: Target information shown above is from the UniProt Consortium.
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