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- 抗原 See all MMAA 抗体
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
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抗原表位
- AA 56-84, N-Term
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适用
- 人, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This MMAA antibody is un-conjugated
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应用范围
- 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 MMAA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human MMAA.
- 亚型
- Ig Fraction
- Top Product
- Discover our top product MMAA Primary Antibody
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anti-Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA) (AA 56-84), (N-Term) antibody
MMAA 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB24782 unconjugated
anti-Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA) (AA 1-418) antibodyMMAA 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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- 应用备注
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For WB starting dilution is: 1:500
For IHC-P starting dilution is: 1:50~100 - 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- 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
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
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- 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.
- 分子量
- 47 kDa
- 基因ID
- 166785
- UniProt
- Q8IVH4
- 途径
- Monocarboxylic Acid Catabolic Process
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