MMAB 抗体 (Center)
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- 抗原 See all MMAB 抗体
- MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
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抗原表位
- Center
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适用
- 人
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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 MMAB antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 小鼠, 牛
- 交叉反应 (详细)
- Mouse (90 %), Bovine (89 %)
- 产品特性
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Rabbit Polyclonal antibody to MMAB (methylmalonic aciduria (cobalamin deficiency) cblB type)
MMAB antibody - 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human MMAB. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product MMAB Primary Antibody
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- 应用备注
- Suggested dilution Reference IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceIHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:500-1:3000*
- 说明
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Positive Control: HepG2
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.69 mg/mL
- 缓冲液
- 1XPBS, 1 % BSA, 20 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
- 别名
- MMAB (MMAB 产品)
- 别名
- ATR antibody, cblB antibody, cob antibody, 9130222L19Rik antibody, methylmalonic aciduria (cobalamin deficiency) cblB type antibody, methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) antibody, MMAB antibody, Mmab antibody
- 背景
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This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group.
Cellular Localization: Mitochondrion - 分子量
- 27 kDa
- 基因ID
- 326625
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