C2orf57 抗体 (Alexa Fluor 594)
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- 抗原 See all C2orf57 products
- C2orf57 (Chromosome 2 Open Reading Frame 57 (C2orf57))
- 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 C2orf57 antibody is conjugated to Alexa Fluor 594
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C2orf57
- 亚型
- IgG
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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
- 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
- C2orf57 (Chromosome 2 Open Reading Frame 57 (C2orf57))
- 别名
- C2orf57 (C2orf57 产品)
- 别名
- testis expressed 44 antibody, TEX44 antibody
- 背景
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Synonyms: Chromosome 2 open reading frame 57, Hypothetical protein LOC165100, MGC35154, Uncharacterized protein C2orf57, CB057_HUMAN.
Background: C2orf57, also known as MGC35154, is a 395 amino acid protein encoded by a gene that maps to human chromosome 2q37.1. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
- 基因ID
- 165100
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