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Anti-AIF-M1 (Y85) Antibody |产品详情|进口榴莲视频免费观看采购网





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    Anti-AIF-M1 (Y85) Antibody
    品牌:Antibodies
    货号:
    规格:50µl
    货期:

    Anti-AIF-M1 (Y85) Antibody

    商品详情 参考文献 相关资料
    Name: Anti-AIF-M1 (Y85) Antibody
    See all AIFM1 primary antibodies
    Description: Rabbit polyclonal antibody to AIF-M1 (Y85)
    Specificity: AIF-M1 (Y85) pAb detects endogenous levels of AIF-M1 protein.
    Applications: WB, IHC, IF
    Reactivity: Human, Mouse, Rat
    Immunogen: Synthetic peptide, corresponding to amino acids 61-110 of Human AIF-M1.
    Host: Rabbit
    Clonality: Polyclonal
    Conjugate: Unconjugated
    Molecular Weight: ~ 67 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 both as NADH oxidoreductase and as regulator of apoptosis. In response to apoptotic stimuli, it is released from the mitochondrion intermembrane space into the cytosol and to the nucleus, where it functions as a proapoptotic factor in a caspase-independent pathway. In contrast, functions as an antiapoptotic factor in normal mitochondria via its NADH oxidoreductase activity. The soluble form (AIFsol) found in the nucleus induces 'parthanatos' i.e. caspase-independent fragmentation of chromosomal DNA. Interacts with EIF3G,and thereby inhibits the EIF3 machinery and protein synthesis, and activates casapse-7 to amplify apoptosis. Plays a critical role in caspase-independent, pyknotic cell death in hydrogen peroxide-exposed cells. Binds to DNA in a sequence-independent manner.
    Tissue Specificity: Detected in muscle and skin fibroblasts (at protein level). Isoform 5 is frequently down-regulated in human cancers.
    Involvement in Disease: Combined oxidative phosphorylation deficiency 6: A mitochondrial disease resulting in a neurodegenerative disorder characterized by psychomotor delay, hypotonia, areflexia, muscle weakness and wasting. Some patients manifest prenatal ventriculomegaly and severe postnatal encephalomyopathy.

    Cowchock syndrome: An X-linked recessive neuromuscular disorder characterized by early childhood onset of a slowly progressive axonal sensorimotor neuropathy associated in some patients with sensorineural deafness and cognitive impairment.

    Deafness, X-linked, 5: A form of hearing loss characterized by absent or severely abnormal auditory brainstem response, abnormal middle ear reflexes, abnormal speech discrimination, loss of outer hair cell function, and cochlear nerve hypoplasia. DFNX5 patients manifest auditory neuropathy with childhood onset, associated with distal sensory impairment affecting the peripheral nervous system.
    Sequence Similarities: Belongs to the FAD-dependent oxidoreductase family.
    Post-Translational Modification: Under normal conditions, a 54-residue N-terminal segment is first proteolytically removed during or just after translocations into the mitochondrial intermembrane space (IMS) by the mitochondrial processing peptidase (MPP) to form the inner-membrane-anchored mature form (AIFmit). During apoptosis, it is further proteolytically processed at amino-acid position 101 leading to the generation of the mature form, which is confined to the mitochondrial IMS in a soluble form (AIFsol). AIFsol is released to the cytoplasm in response to specific death signals, and translocated to the nucleus, where it induces nuclear apoptosis in a caspase-independent manner.
    Cellular locations: Mitochondrion intermembrane space. Mitochondrion inner membrane. Cytoplasm. Nucleus. Cytoplasm > Perinuclear region.

    Proteolytic cleavage during or just after translocations into the mitochondrial intermembrane space (IMS) results in the formation of an inner-membrane-anchored mature form (AIFmit). During apoptosis, further proteolytic processing leads to a mature form, which is confined to the mitochondrial IMS in a soluble form (AIFsol). AIFsol is released to the cytoplasm in response to specific death signals, and translocated to the nucleus, where it induces nuclear apoptosis. Colocalizes with EIF3G in the nucleus and perinuclear region.
    Database Links:
  1. Entrez Gene: 51060?Human
  2. Entrez Gene: 9131?Human
  3. Entrez Gene: 26926?Mouse
  4. Entrez Gene: 83533?Rat
  5. Omim: 300169?Human
  6. SwissProt: O95831?Human
  7. SwissProt: Q9Z0X1?Mouse
  8. SwissProt: Q9JM53?Rat
  9. Unigene: 424932?Human
  10. Unigene: 476033?Human
  11. Unigene: 240434?Mouse
  12. Unigene: 203165?Rat
  13. Synonyms:
  14. AIF Antibody
  15. AIFM1 Antibody
  16. AIFM1_HUMAN Antibody
  17. AIFsh2 Antibody
  18. Apoptosis inducing factor Antibody
  19. Apoptosis inducing factor 1, mitochondrial Antibody
  20. Apoptosis inducing factor, mitochondrion associated, 1 Antibody
  21. Apoptosis-inducing factor Antibody
  22. Apoptosis-inducing factor 1 Antibody
  23. Apoptosis-inducing factor 1, mitochondrial Antibody
  24. Apoptosis-inducing factor, mitochondrion-associated, 1 Antibody
  25. CMTX4 Antibody
  26. COWCK Antibody
  27. COXPD6 Antibody
  28. Harlequin Antibody
  29. Hq Antibody
  30. mAIF Antibody
  31. MGC111425 Antibody
  32. MGC5706 Antibody
  33. mitochondrial Antibody
  34. Neuropathy, axonal motor-sensory, with deafness and mental retardation Antibody
  35. neuropathy, axonal, motor-sensory with deafness and mental retardation (Cowchock syndrome) Antibody
  36. PDCD 8 Antibody
  37. PDCD8 Antibody
  38. Programmed cell death 8 Antibody
  39. Programmed cell death 8 (apoptosis inducing factor) Antibody
  40. Programmed cell death 8 isoform 1 Antibody
  41. Programmed cell death 8 isoform 2 Antibody
  42. Programmed cell death 8 isoform 3 Antibody
  43. Programmed cell death protein 8 Antibody
  44. Programmed cell death protein 8 mitochondrial Antibody
  45. Programmed cell death protein 8 mitochondrial precursor Antibody
  46. Striatal apoptosis inducing factor Antibody
  47. Information: Target information shown above is from the UniProt Consortium.
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