SUCLA2 抗体
Our Local Distributor
北京 101111
Quick Overview for SUCLA2 抗体 (ABIN2856701)
抗原
See all SUCLA2 抗体适用
宿主
克隆类型
标记
应用范围
质量等级
-
-
交叉反应
- 人, 小鼠
-
产品特性
-
Rabbit Polyclonal antibody to SUCLA2 (succinate-CoA ligase, ADP-forming, beta subunit)
SUCLA2 antibody [N2C3] -
纯化方法
- Purified by antigen-affinity chromatography.
-
免疫原
- Recombinant protein encompassing a sequence within the center region of human SUCLA2. The exact sequence is proprietary.
-
亚型
- IgG
-
-
anti-Succinate-CoA Ligase, ADP-Forming, beta Subunit (SUCLA2) (AA 1-180) antibody
SUCLA2 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Succinate-CoA Ligase, ADP-Forming, beta Subunit (SUCLA2) (Internal Region) antibodySUCLA2 适用: 人, 小鼠, 大鼠 WB, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
-
说明
-
Positive Control: Mouse brain , HepG2 , Molt-4 , HeLa
Validation: KO/KD
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 1 mg/mL
-
缓冲液
- 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
-
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
- 4 °C,-20 °C
-
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.
-
-
- SUCLA2 (Succinate-CoA Ligase, ADP-Forming, beta Subunit (SUCLA2))
-
别名
- succinate-CoA ligase ADP-forming beta subunit
-
背景
-
Succinyl-CoA synthetase (SCS) is a mitochondrial matrix enzyme that acts as a heterodimer, being composed of an invariant alpha subunit and a substrate-specific beta subunit. The protein encoded by this gene is an ATP-specific SCS beta subunit that dimerizes with the SCS alpha subunit to form SCS-A, an essential component of the tricarboxylic acid cycle. SCS-A hydrolyzes ATP to convert succinate to succinyl-CoA. Defects in this gene are a cause of myopathic mitochondrial DNA depletion syndrome. A pseudogene of this gene has been found on chromosome 6.
Cellular Localization: Mitochondrion -
分子量
- 50 kDa
-
基因ID
- 8803
-
UniProt
- Q9P2R7
抗原
-
