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alpha KGDHC 抗体 (C-Term)

alphaKGDHC 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB32469 unconjugated
产品编号 ABIN657365
发货至: 中国
  • 抗原 See all alpha KGDHC (alphaKGDHC) 抗体
    alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))
    抗原表位
    • 7
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    AA 381-410, C-Term
    适用
    • 26
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 25
    • 1
    克隆类型
    • 25
    • 1
    多克隆
    标记
    • 15
    • 3
    • 3
    • 3
    • 1
    • 1
    This alpha KGDHC antibody is un-conjugated
    应用范围
    • 22
    • 15
    • 14
    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This OGDH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 381-410 amino acids from the C-terminal region of human OGDH.
    克隆位点
    RB32469
    亚型
    Ig Fraction
    Top Product
    Discover our top product alphaKGDHC Primary Antibody
  • 应用备注
    WB: 1:1000. IHC-P: 1:10~50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in 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.
    储存条件
    4 °C,-20 °C
    储存方法
    OGDH Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
    有效期
    6 months
  • 抗原
    alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))
    别名
    OGDH (alphaKGDHC 产品)
    背景
    This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex. This complex catalyzes the overall conversion of 2-oxoglutarate (alpha-ketoglutarate) to succinyl-CoA and CO(2) during the Krebs cycle. The protein is located in the mitochondrial matrix and uses thiamine pyrophosphate as a cofactor. A congenital deficiency in 2-oxoglutarate dehydrogenase activity is believed to lead to hypotonia, metabolic acidosis, and hyperlactatemia. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
    分子量
    115935
    基因ID
    4967
    NCBI登录号
    NP_001003941, NP_001158508, NP_002532
    UniProt
    Q02218
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