DMWD 抗体 (AA 501-600) (Cy7)
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- 抗原 See all DMWD 抗体
- DMWD (Dystrophia Myotonica, WD Repeat Containing (DMWD))
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抗原表位
- AA 501-600
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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 DMWD antibody is conjugated to Cy7
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Cow
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human DMWD/DMRN9
- 亚型
- IgG
- Top Product
- Discover our top product DMWD Primary Antibody
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- DMWD (Dystrophia Myotonica, WD Repeat Containing (DMWD))
- 别名
- DMWD/DMRN9 (DMWD 产品)
- 别名
- D19S593E antibody, DMR-N9 antibody, DMRN9 antibody, gene59 antibody, DMWD antibody, Dm9 antibody, DM1 locus, WD repeat containing antibody, dystrophia myotonica, WD repeat containing antibody, dystrophia myotonica-containing WD repeat motif antibody, DMWD antibody, Dmwd antibody
- 背景
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Synonyms: dystrophia myotonica containing WD repeat mot,D19S593E, DM 9, DM9, DMR N9, DMR N9 protein, DMRN 9, DMRN9, DMWD, DMWD_HUMAN, Dystrophia myotonica containing WD repeat mot, Dystrophia myotonica containing WD repeat mot protein, Dystrophia myotonica WD repeat containing protein, Dystrophia myotonica WD repeat-containing protein, Dystrophia myotonica-containing WD repeat mot protein, Gene59, Protein 59, Protein DMR-N9.
Background: DMWD is a 674 amino acid protein containing five WD repeats. DMWD may play a role in the development of mental symptoms in severe cases of myotonic dystrophy, a chronic multisystemic disease characterized by wasting of the muscles, heart conduction defects, cataracts, endocrine changes and myotonia. The DMWD gene is located upstream of the DMPK gene and is prominently expressed in tissues affected in myotonic dystrophy patients. DMWD may also contribute to regulation in meiosis. DMWD is expressed in kidney and spleen, with strongest expression in brain, liver and testis. The gene encoding DMWD maps to human chromosome 19q13.32 and mouse chromosome 7 A3.
- 基因ID
- 1762
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