Strumpellin 抗体 (C-Term)
This anti-Strumpellin antibody is a 兔 多克隆 antibody detecting Strumpellin in WB 和 IHC (p). Suitable for 人.
Quick Overview for Strumpellin 抗体 (C-Term) (ABIN7465862)
抗原
See all Strumpellin (WASHC5) 抗体
Strumpellin (WASHC5)
(WASH Complex Subunit 5 (WASHC5))
适用
人
宿主
兔
克隆类型
多克隆
标记
This Strumpellin antibody is un-conjugated
应用范围
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
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抗原表位
- C-Term
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交叉反应
- 人
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein encompassing a sequence within the C-terminus region of human Strumpellin. The exact sequence is proprietary.
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亚型
- IgG
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anti-WASH Complex Subunit 5 (WASHC5) (AA 380-530) antibody
WASHC5 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-WASH Complex Subunit 5 (WASHC5) (C-Term) antibodyWASHC5 适用: 人, 小鼠, 大鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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说明
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Positive Control: HeLa
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal
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储存液
- Thimerosal (Merthiolate)
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注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
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别名
- WASH complex subunit 5
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背景
- WASH complex subunit 5 , KIAA0196 , RTSC , RTSC1 , SPG8,This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease, a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases. [provided by RefSeq]
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分子量
- 134 kDa
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基因ID
- 9897
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UniProt
- Q12768
抗原
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