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L2HGDH 抗体 (AA 1-220)

L2HGDH 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7268160
发货至: 中国
  • 抗原 See all L2HGDH 抗体
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    抗原表位
    • 7
    • 7
    • 7
    • 6
    • 5
    • 5
    • 3
    • 2
    • 1
    • 1
    AA 1-220
    适用
    • 30
    • 15
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    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
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    原理
    L2HGDH Rabbit pAb
    序列
    MVPALRYLVG ACGRARGLFA GGSPGACGFA SGRPRPLCGG SRSASTSSFD IVIVGGGIVG LASARALILR HPSLSIGVLE KEKDLAVHQT GHNSGVIHSG IYYKPESLKA KLCVQGAALL YEYCQQKGIS YKQCGKLIVA VEQEEIPRLQ ALYEKGLQNG VPGLRLIQQE DIKKKEPYCR GLMAIDCPHT GIVDYRQVAL SFAQDFQEAG GSVLTNFEVK
    交叉反应
    人, 小鼠
    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 1-220 of human L2HGDH (NP_079160.1).
    亚型
    IgG
    Top Product
    Discover our top product L2HGDH Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000,IF,1:50 - 1:200
    限制
    仅限研究用
  • 状态
    Liquid
    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
    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))
    别名
    L2HGDH (L2HGDH 产品)
    别名
    RGD1306250 antibody, C14orf160 antibody, BC016226 antibody, L-2-hydroxyglutarate dehydrogenase antibody, L2hgdh antibody, L2HGDH antibody
    背景
    This 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.,L2HGDH,C14orf160,L2HGA,Signal Transduction,Cell Biology & Developmental Biology,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,L2HGDH
    分子量
    48kDa/50kDa
    基因ID
    79944
    UniProt
    Q9H9P8
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