SDHA 抗体 (N-Term)
Quick Overview for SDHA 抗体 (N-Term) (ABIN2855128)
抗原
See all SDHA 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- N-Term
-
产品特性
-
Rabbit Polyclonal antibody to SDHA (succinate dehydrogenase complex, subunit A, flavoprotein (Fp))
SDHA antibody -
纯化方法
- Purified by antigen-affinity chromatography.
-
免疫原
- Recombinant protein encompassing a sequence within the N-terminus region of human SDHA. The exact sequence is proprietary.
-
亚型
- IgG
-
-
-
-
应用备注
- Suggested dilution Reference ICC/IF 1:100-1:1000* IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceICC/IF1:100-1:1000* IHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:500-1:3000*
-
说明
-
Positive Control: Molt-4 , mouse brain
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 0.22 mg/mL
-
缓冲液
- 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
-
储存液
- Thimerosal (Merthiolate)
-
注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
储存条件
- -20 °C
-
储存方法
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
-
-
-
: "Light-driven activation of mitochondrial proton-motive force improves motor behaviors in a Drosophila model of Parkinson's disease." in: Communications biology, Vol. 2, pp. 424, (2020) (PubMed).
-
: "Light-driven activation of mitochondrial proton-motive force improves motor behaviors in a Drosophila model of Parkinson's disease." in: Communications biology, Vol. 2, pp. 424, (2020) (PubMed).
-
- SDHA (Succinate Dehydrogenase Complex, Subunit A, Flavoprotein (Fp) (SDHA))
-
别名
- SDHA
-
背景
-
This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29.
Cellular Localization: Mitochondrion inner membrane -
分子量
- 73 kDa
-
基因ID
- 6389
抗原
-