Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) Peptide
Our Local Distributor
北京 101111
Quick Overview for Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) Peptide (ABIN8105037)
抗原
资源
应用范围
-
-
原理
- ACADM Peptide
-
-
Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) peptide
MCAD 适用: 人 宿主: 合成 BP, Imm
-
-
应用备注
- Optimal working dilution should be determined by the investigator.
-
说明
-
This is a synthetic peptide designed for use in combination with anti-ACADM antibody ( ARP32788_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
-
限制
- 仅限研究用
-
-
-
状态
- Lyophilized
-
溶解方式
- Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
-
缓冲液
- Lyophilized powder
-
储存条件
- -20 °C
-
储存方法
- For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
-
-
- Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD)
-
背景
-
Background Information: ACADM Is the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Clinical phenotypes are associated with ACADM hereditary deficiency.This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Alternative Symbols: ACAD1, MCAD, MCADH
-
分子量
- 46kDa
-
基因ID
- 34
-
NCBI登录号
- NP_000007
-
UniProt
- P11310
抗原
-
