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MMAA 抗体 (N-Term)

MMAA 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN953465
发货至: 中国
  • 抗原 See all MMAA 抗体
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    抗原表位
    • 10
    • 8
    • 4
    • 2
    • 1
    AA 63-92, N-Term
    适用
    • 34
    • 23
    • 16
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 31
    • 3
    克隆类型
    • 33
    • 1
    多克隆
    标记
    • 10
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MMAA antibody is un-conjugated
    应用范围
    • 34
    • 14
    • 13
    • 12
    • 6
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    特异性
    This antibody recognizes Human and Mouse MMAA (N-term).
    纯化方法
    Protein A column, followed by peptide affinity purification
    免疫原
    KLH conjugated synthetic peptide between 63~92 amino acids from the N-terminal region of human MMAA
    亚型
    Ig Fraction
    Top Product
    Discover our top product MMAA 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 containing 0.09 % (W/V) Sodium Azide as preservative
    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 undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    别名
    MMAA (MMAA 产品)
    别名
    2810018E08Rik antibody, AI840684 antibody, cblA antibody, methylmalonic aciduria (cobalamin deficiency) type A antibody, methylmalonic aciduria (cobalamin deficiency) cblA type antibody, Mmaa antibody, MMAA antibody
    背景
    The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.Synonyms: MGC120010, MGC120011, MGC120012, Methylmalonic aciduria type A, Methylmalonic aciduria type A protein, mitochondrial
    分子量
    46538 Da
    基因ID
    166785
    NCBI登录号
    NP_758454
    途径
    Monocarboxylic Acid Catabolic Process
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