C8orf47 抗体 (AbBy Fluor® 555)
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- 抗原 See all C8orf47 (C8ORF47) products
- C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))
- 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 C8orf47 antibody is conjugated to AbBy Fluor® 555
- 应用范围
- Western Blotting (WB)
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C8orf47
- 亚型
- IgG
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anti-Chromosome 8 Open Reading Frame 47 (C8ORF47) (AA 1-100) antibody
C8ORF47 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 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
- 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
- -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
- C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))
- 别名
- C8orf47 (C8ORF47 产品)
- 别名
- glutamate rich 5 antibody, ERICH5 antibody
- 背景
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Synonyms: C8orf47, CH047_HUMAN, Chromosome 8 open reading frame 47, Uncharacterized protein C8orf47.
Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf47 gene product has been provisionally designated C8orf47 pending further characterization.
- 基因ID
- 203111
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