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ACADL 抗体 (AA 31-210)

ACADL 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1678519
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
    • 8
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 31-210
    适用
    • 58
    • 29
    • 6
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    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
    • 35
    • 26
    • 26
    • 8
    • 7
    • 6
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    序列
    GGEERLETPS AKKLTDIGIR RIFSPEHDIF RKSVRKFFQE EVIPHHSEWE KAGEVSREVW EKAGKQGLLG VNIAEHLGGI GGDLYSAAIV WEEQAYSNCS GPGFSIHSGI VMSYITNHGS EEQIKHFIPQ MTAGKCIGAI AMTEPGAGSD LQGIKTNAKK DGSDWILNGS KVFISNGSLS
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Polyclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 31-210 of human ACADL (NP_001599.1).
    亚型
    IgG
    Top Product
    Discover our top product ACADL Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    限制
    仅限研究用
  • 缓冲液
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))
    别名
    ACADL (ACADL 产品)
    背景
    The protein encoded by this gene 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.,ACADL,ACAD4,LCAD,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Lipid Metabolism,Cardiovascular,Lipids,Fatty Acids,ACADL
    分子量
    47 kDa
    基因ID
    33
    UniProt
    P28330
    途径
    Monocarboxylic Acid Catabolic Process
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