C2orf40 抗体 (AbBy Fluor® 350)
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- 抗原 See all C2orf40 抗体
- C2orf40 (Chromosome 2 Open Reading Frame 40 (C2orf40))
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适用
- 人, 小鼠, 大鼠
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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 C2orf40 antibody is conjugated to AbBy Fluor® 350
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ECRG4/C2orf40
- 亚型
- IgG
- Top Product
- Discover our top product C2orf40 Primary Antibody
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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
- C2orf40 (Chromosome 2 Open Reading Frame 40 (C2orf40))
- 别名
- ECRG4 (C2orf40 产品)
- 别名
- ECRG4 antibody, ecrg4 antibody, ecrg4-A antibody, Ecrg4 antibody, chromosome 2 open reading frame, human C2orf40 antibody, chromosome 13 open reading frame, human C2orf40 antibody, chromosome 11 open reading frame, human C2orf40 antibody, chromosome 2 open reading frame 40 antibody, chromosome 2 open reading frame 40 L homeolog antibody, RIKEN cDNA 1500015O10 gene antibody, similar to RIKEN cDNA 1500015O10 antibody, C2H2orf40 antibody, C13H2orf40 antibody, C11H2orf40 antibody, C2orf40 antibody, c2orf40.L antibody, 1500015O10Rik antibody, RGD1305645 antibody
- 背景
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Synonyms: AUGN_HUMAN, Augurin, C2orf40, Esophageal cancer-related gene 4 protein.
Background: ECRG4, also known as augurin or C2orf40, is a 148 amino acid secreted protein. Belonging to the augurin family, ECRG4 is thought to be a hormone. It has also been suggested that ECRG4 may act as a tumor suppressor. The gene that encodes ECRG4 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes, making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid 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 due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes.
- 基因ID
- 84417
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