SPG7 抗体 (AA 384-568)
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北京 101111
Quick Overview for SPG7 抗体 (AA 384-568) (ABIN1886423)
抗原
See all SPG7 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 384-568
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 384 and 568 of SPG7
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anti-Spastic Paraplegia 7 (SPG7) (AA 300-573) antibody
SPG7 适用: 人, 小鼠 WB, IF, FACS 宿主: 小鼠 Monoclonal 1C12 unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 300-573) antibodySPG7 适用: 人 WB, IF, FACS 宿主: 小鼠 Monoclonal 3H10 unconjugated
anti-Spastic Paraplegia 7 (SPG7) antibodySPG7 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 25GB5505 unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 1-250) antibodySPG7 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 1-795) antibodySPG7 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 1-795) antibodySPG7 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 115-141) antibodySPG7 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB23654 unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 114-141), (Middle Region) antibodySPG7 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000 -
限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- 0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
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储存液
- Thimerosal (Merthiolate)
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注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- SPG7 (Spastic Paraplegia 7 (SPG7))
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别名
- SPG7
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背景
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This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family.Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis.Two transcript variants encoding distinct isoforms have been identified for this gene.Mutations associated with this gene cause autosomal recessive spastic paraplegia 7.[provided by RefSeq]
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分子量
- 88 kDa
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基因ID
- 6687
抗原
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