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Anti-ERAB (E135) Antibody |产品详情|进口榴莲视频免费观看采购网





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    Anti-ERAB (E135) Antibody
    品牌:Antibodies
    货号:
    规格:50µl
    货期:

    Anti-ERAB (E135) Antibody

    商品详情 参考文献 相关资料
    Name: Anti-ERAB (E135) Antibody
    See all ERAB primary antibodies
    Description: Rabbit polyclonal antibody to ERAB (E135)
    Specificity: ERAB (E135) pAb detects endogenous levels of ERAB protein.
    Applications: WB, IHC
    Reactivity: Human, Mouse, Rat
    Immunogen: Synthetic peptide, corresponding to amino acids 102-150 of Human ERAB.
    Host: Rabbit
    Clonality: Polyclonal
    Conjugate: Unconjugated
    Molecular Weight: ~ 27 kDa
    Purity: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
    Product Form: 1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
    Function: Functions in mitochondrial tRNA maturation. Part of mitochondrial ribonuclease P, an enzyme composed of MRPP1/TRMT10C, MRPP2/HSD17B10 and MRPP3/KIAA0391, which cleaves tRNA molecules in their 5'-ends. Catalyzes the beta-oxidation at position 17 of androgens and estrogens and has 3-alpha-hydroxysteroid dehydrogenase activity with androsterone. Catalyzes the third step in the beta-oxidation of fatty acids. Carries out oxidative conversions of 7-alpha-OH and 7-beta-OH bile acids. Also exhibits 20-beta-OH and 21-OH dehydrogenase activities with C21 steroids. By interacting with intracellular amyloid-beta, it may contribute to the neuronal dysfunction associated with Alzheimer disease (AD).
    Tissue Specificity: Ubiquitously expressed in normal tissues but is overexpressed in neurons affected in AD.
    Involvement in Disease: 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: A disorder that leads to neurological abnormalities, including psychomotor retardation and, in virtually all patients, loss of mental and motor skills.

    Mental retardation, X-linked, syndromic, 10: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRXS10 patients manifest mild mental retardation, choreoathetosis and abnormal behavior.

    Mental retardation, X-linked 17: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations.
    Sequence Similarities: Belongs to the short-chain dehydrogenases/reductases (SDR) family.
    Cellular locations: Mitochondrion.
    Database Links:
  1. Entrez Gene: 3028?Human
  2. Entrez Gene: 15108?Mouse
  3. Entrez Gene: 63864?Rat
  4. Omim: 300256?Human
  5. SwissProt: Q99714?Human
  6. SwissProt: O08756?Mouse
  7. SwissProt: O70351?Rat
  8. Unigene: 171280?Human
  9. Unigene: 6994?Mouse
  10. Unigene: 2700?Rat
  11. Synonyms:
  12. 17 beta hydroxysteroid dehydrogenase 10 Antibody
  13. 17 beta hydroxysteroid dehydrogenase type 10 Antibody
  14. 17-beta-HSD 10 Antibody
  15. 17-beta-hydroxysteroid dehydrogenase 10 Antibody
  16. 17b HSD10 Antibody
  17. 3 hydroxy 2 methylbutyryl CoA dehydrogenase Antibody
  18. 3 hydroxyacyl CoA dehydrogenase type 2 Antibody
  19. 3 hydroxyacyl CoA dehydrogenase type II Antibody
  20. 3-hydroxy-2-methylbutyryl-CoA dehydrogenase Antibody
  21. 3-hydroxyacyl-CoA dehydrogenase type II Antibody
  22. 3-hydroxyacyl-CoA dehydrogenase type-2 Antibody
  23. AB binding alcohol dehydrogenase Antibody
  24. ABAD Antibody
  25. Ads9 Antibody
  26. Amyloid beta binding polypeptide Antibody
  27. Amyloid beta peptide binding alcohol dehydrogenase Antibody
  28. Amyloid beta peptide binding protein Antibody
  29. CAMR Antibody
  30. DUPXp11.22 Antibody
  31. Endoplasmic Reticulum Amyloid Binding Protein Antibody
  32. Endoplasmic reticulum associated amyloid beta peptide binding protein Antibody
  33. Endoplasmic reticulum-associated amyloid beta-peptide-binding protein Antibody
  34. ER associated amyloid beta-binding protein Antibody
  35. ERAB Antibody
  36. HADH 2 Antibody
  37. HADH2 Antibody
  38. HCD 2 Antibody
  39. HCD2 Antibody
  40. HCD2_HUMAN Antibody
  41. Hsd17b10 Antibody
  42. Hydroxyacyl CoA Dehydrogenase type II Antibody
  43. Hydroxyacyl Coenzyme A dehydrogenase type II Antibody
  44. Hydroxysteroid (17 beta) dehydrogenase 10 Antibody
  45. Mental retardation X linked syndromic 11 Antibody
  46. MHBD Antibody
  47. Mitochondrial L3 Hydroxyacyl CoA Dehydrogenase Antibody
  48. Mitochondrial ribonuclease P protein 2 Antibody
  49. Mitochondrial RNase P protein 2 Antibody
  50. MRPP2 Antibody
  51. MRX17 Antibody
  52. SCHAD Antibody
  53. SDR5C1 Antibody
  54. Short chain dehydrogenase/reductase family 5C member 1 Antibody
  55. Short chain L 3 hydroxyacyl CoA dehydrogenase type 2 Antibody
  56. Short chain type dehydrogenase/reductase XH98G2 Antibody
  57. Short-chain type dehydrogenase/reductase XH98G2 Antibody
  58. Type 10 17b HSD Antibody
  59. Type 10 17beta hydroxysteroid dehydrogenase Antibody
  60. Type II HADH Antibody
  61. XH98G2 Antibody
  62. Information: Target information shown above is from the UniProt Consortium.
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