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ACADL 抗体 (AA 14-43)

ACADL 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5647677
发货至: 中国
  • 抗原 See all ACADL 抗体
    ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
    抗原表位
    • 15
    • 15
    • 10
    • 8
    • 7
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 14-43
    适用
    • 58
    • 28
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 68
    • 1
    克隆类型
    • 69
    多克隆
    标记
    • 22
    • 7
    • 6
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This ACADL antibody is un-conjugated
    应用范围
    • 50
    • 34
    • 26
    • 26
    • 8
    • 8
    • 6
    • 2
    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Antigen affinity purified
    免疫原
    A portion of amino acids 14-43 from the human protein was used as the immunogen for this ACADL antibody.
    亚型
    Ig Fraction
    Top Product
    Discover our top product ACADL Primary Antibody
  • 应用备注
    Western blot: 1:500-1000
    限制
    仅限研究用
  • 缓冲液
    In 1X PBS, pH 7.4, with 0.09 % sodium azide
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Aliquot the ACADL antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原
    ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
    别名
    ACADL (ACADL 产品)
    别名
    zgc:55656 antibody, ACAD4 antibody, LCAD antibody, ACOADA antibody, AA960361 antibody, AU018452 antibody, C79855 antibody, acyl-CoA dehydrogenase long chain antibody, acyl-CoA dehydrogenase, long chain antibody, acyl-CoA dehydrogenase, long chain L homeolog antibody, acyl-Coenzyme A dehydrogenase, long-chain antibody, acadl antibody, ACADL antibody, Acadl antibody, acadl.L antibody
    背景
    Long-chain specific acyl-CoA dehydrogenase, mitochondrial belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
    UniProt
    P28330
    途径
    Monocarboxylic Acid Catabolic Process
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