Recombinant人OPA1 protein (ab114289)

概述

描述

  • 性质Recombinant
  • 来源Wheat germ
  • 氨基酸序列
    • AccessionO60313
    • 种属Human
    • 序列NHCNLCRRGFYYYQRHFVDSELECNDVVLFWRIQRMLAITANTLRQQLTN TEVRRLEKNVKEVLEDFAEDGEKKIKLLTGKRVQLAEDLKKVREIQEKLD AFIEALHQEK
    • 分子量38 kDa including tags
    • 氨基酸851 to 960

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技术指标

Our Abpromise guarantee covers the use of ab114289 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • 应用

    Western blot

    ELISA

    SDS-PAGE

  • 形式Liquid
  • 补充说明Protein concentration is above or equal to 0.05 mg/ml.
    Best used within three months from the date of receipt.
  • Concentration information loading...

制备和贮存

  • 稳定性和存储

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

常规信息

  • 别名
    • Dynamin like 120 kDa protein
    • Dynamin like 120 kDa protein, mitochondrial
    • Dynamin-like 120 kDa protein, form S1
    • FLJ12460
    • Juvenile kjer type optic atrophy
    • KIAA0567
    • KJER type
    • Large GTP binding protein
    • largeG
    • MGM1
    • Mitochondrial dynamin like 120 kDa protein
    • Mitochondrial dynamin like GTPase
    • NPG
    • NTG
    • OAK
    • OPA 1
    • opa1
    • OPA1 gene
    • OPA1_HUMAN
    • OPTIC ATROPHY 1
    • Optic atrophy 1 (autosomal dominant)
    • Optic atrophy 1 gene protein
    • Optic atrophy 1 homolog (human)
    • Optic atrophy protein 1
    • Optic atrophy protein 1 homolog
    see all
  • 功能Dynamin-related GTPase required for mitochondrial fusion and regulation of apoptosis. May form a diffusion barrier for proteins stored in mitochondrial cristae. Proteolytic processing in response to intrinsic apoptotic signals may lead to disassembly of OPA1 oligomers and release of the caspase activator cytochrome C (CYCS) into the mitochondrial intermembrane space.
  • 组织特异性Highly expressed in retina. Also expressed in brain, testis, heart and skeletal muscle. Isoform 1 expressed in retina, skeletal muscle, heart, lung, ovary, colon, thyroid gland, leukocytes and fetal brain. Isoform 2 expressed in colon, liver, kidney, thyroid gland and leukocytes. Low levels of all isoforms expressed in a variety of tissues.
  • 疾病相关Defects in OPA1 are a cause of optic atrophy type 1 (OPA1) [MIM:165500]. OPA1 is a dominantly inherited optic neuropathy occurring in 1 in 50,000 individuals that features progressive loss in visual acuity leading, in many cases, to legal blindness.
    Defects in OPA1 are the cause of optic atrophy 1 with deafness (OPA1D) [MIM:125250]. Some individuals with mutations in OPA1 manifest also ophthalmoplegia and myopathy.
  • 序列相似性Belongs to the dynamin family.
  • 翻译后修饰PARL-dependent proteolytic processing releases an antiapoptotic soluble form not required for mitochondrial fusion.
  • 细胞定位Mitochondrion inner membrane. Mitochondrion intermembrane space.
  • Information by UniProt

Recombinant Human OPA1 protein 图像

  • ab114289 analysed on a 12.5% SDS-PAGE gel stained with Coomassie Blue.

Recombinant Human OPA1 protein (ab114289)参考文献

ab114289 has not yet been referenced specifically in any publications.

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