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L2HGDH 抗体 (Middle Region)

L2HGDH 适用: 人, 小鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN951995
发货至: 中国
  • 抗原 See all L2HGDH 抗体
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    抗原表位
    • 7
    • 7
    • 6
    • 6
    • 5
    • 5
    • 4
    • 1
    • 1
    • 1
    AA 139-167, Middle Region
    适用
    • 30
    • 14
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 35
    克隆类型
    • 35
    多克隆
    标记
    • 17
    • 6
    • 4
    • 4
    • 2
    • 2
    This L2HGDH antibody is un-conjugated
    应用范围
    • 26
    • 24
    • 9
    • 2
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    特异性
    This antibody detects L2HGDH/ Duranin.
    交叉反应 (详细)
    Species reactivity (tested):Human, Mouse
    纯化方法
    Purified through a protein A column; followed by peptide affinity purification.
    免疫原
    Synthetic peptide - KLH conjugated - corresponding to the central region (between 139-167aa) of human L2HGDH/Duranin.
    亚型
    Ig Fraction
    Top Product
    Discover our top product L2HGDH Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.25 mg/mL
    缓冲液
    PBS with 0.09 % (W/V) 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.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    别名
    Duranin (L2HGDH 产品)
    别名
    RGD1306250 antibody, C14orf160 antibody, BC016226 antibody, L-2-hydroxyglutarate dehydrogenase antibody, L2hgdh antibody, L2HGDH antibody
    背景
    The L2HGDH gene encodes L-2-hydroxyglutarate dehydrogenase, a FAD-dependent enzyme that oxidizes L-2-hydroxyglutarate to alpha-ketoglutarate in a variety of mammalian tissues. Mutations in this gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder resulting in moderate to severe mental retardation.Synonyms: C14orf160, L-2-hydroxyglutarate dehydrogenase, L2HGDH, hydroxyglutarate dehydrogenase
    基因ID
    79944
    NCBI登录号
    NP_079160
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