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 Anti-ELOVL5 Antibody |产品详情|进口榴莲视频免费观看采购网





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    Anti-ELOVL5 Antibody
    品牌:Antibodies
    货号:
    规格:50µl
    货期:

    Anti-ELOVL5 Antibody

    商品详情 参考文献 相关资料
    Name: Anti-ELOVL5 Antibody
    See all ELOVL5 primary antibodies
    Description: Rabbit polyclonal antibody to ELOVL5
    Specificity: The antibody detects endogenous levels of total ELOVL5 protein.
    Applications: WB, IHC
    Reactivity: Human
    Immunogen: Synthesized peptide derived from internal of human ELOVL5.
    Host: Rabbit
    Clonality: Polyclonal
    Conjugate: Unconjugated
    Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
    Concentration: 1.0mg / ml
    Formulation: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
    Storage: Store at -20?C
    Function: Catalyzes the first and rate-limiting reaction of the four that constitute the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process, allows the addition of 2 carbons to the chain of long- and very long-chain fatty acids/VLCFAs per cycle. Condensing enzyme that acts specifically toward polyunsaturated acyl-CoA with the higher activity toward C18:3(n-6) acyl-CoA. May participate in the production of monounsaturated and of polyunsaturated VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators.
    Tissue Specificity: Ubiquitous. Highly expressed in the adrenal gland and testis. Weakly expressed in prostate, lung and brain. Expressed in the cerebellum.
    Involvement in Disease: Spinocerebellar ataxia 38: A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA38 is an autosomal dominant form characterized by *****-onset of slowly progressive gait ataxia accompanied by nystagmus. Brain MRI shows cerebellar atrophy.
    Sequence Similarities: Belongs to the ELO family. ELOVL5 subfamily.
    Cellular locations: Endoplasmic reticulum membrane. Cell projection > Dendrite.

    In Purkinje cells, the protein localizes to the soma and proximal portion of the dendritic tree.
    Database Links:
  1. Entrez Gene: 60481?Human
  2. Omim: 611805?Human
  3. SwissProt: Q9NYP7?Human
  4. Unigene: 725124?Human
  5. Synonyms:
  6. 3 keto acyl CoA synthase ELOVL5 Antibody
  7. 3-keto acyl-CoA synthase Elovl5 Antibody
  8. dJ483K16.1 Antibody
  9. Elongation of very long chain fatty acids like 5 Antibody
  10. Elongation of very long chain fatty acids protein 5 Antibody
  11. ELOV5_HUMAN Antibody
  12. ELOVL 5 Antibody
  13. ELOVL family member 5 Antibody
  14. ELOVL family member 5 elongation of long chain fatty acids Antibody
  15. ELOVL family member 5, elongation of long chain fatty acids (FEN1/Elo2, SUR4/Elo3-like, yeast) Antibody
  16. ELOVL fatty acid elongase 5 Antibody
  17. ELOVL2 Antibody
  18. ELOVL5 Antibody
  19. Fatty acid elongase 1 Antibody
  20. hELO1 Antibody
  21. Homolog of yeast long chain polyunsaturated fatty acid elongation enzyme 2 Antibody
  22. OTTHUMP00000017867 Antibody
  23. RP3 483K16.1 Antibody
  24. RP3-483K16.1 Antibody
  25. Information: Target information shown above is from the UniProt Consortium.
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