SPG7 抗体 (Middle Region)
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Quick Overview for SPG7 抗体 (Middle Region) (ABIN953990)
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 114-141, Middle Region
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特异性
- This antibody recognizes Paraplegin / SPG7.
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交叉反应 （详细）
- Species reactivity (tested):Human
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纯化方法
- Purified through a Protein A column followed by peptide affinity purification
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免疫原
- Synthetic peptide - KLH conjugated - corresponding to the central region (between 114-141aa) of human Paraplegin / SPG7
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亚型
- Ig Fraction
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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
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS with 0.09 % (W/V) Sodium azide
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储存液
- Sodium azide
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注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- SPG7 (Spastic Paraplegia 7 (SPG7))
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别名
- Paraplegin / SPG7
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背景
- The SPG7 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.Synonyms: CAR, CMAR, PGN, Spastic paraplegia 7 protein
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基因ID
- 6687
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NCBI登录号
- NP_003110
抗原
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