C2orf47 抗体
Quick Overview for C2orf47 抗体 (ABIN1385958)
抗原
适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human C2ORF47
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亚型
- IgG
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anti-Chromosome 2 Open Reading Frame 47 (C2orf47) (AA 1-291) antibody
C2orf47 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 2 Open Reading Frame 47 (C2orf47) (C-Term) antibodyC2orf47 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, Bat, Hamster, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 2 Open Reading Frame 47 (C2orf47) (AA 190-219), (C-Term) antibodyC2orf47 适用: 人 WB 宿主: 兔 Polyclonal RB45068 unconjugated
anti-Chromosome 2 Open Reading Frame 47 (C2orf47) (Middle Region) antibodyC2orf47 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 2 Open Reading Frame 47 (C2orf47) antibodyC2orf47 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- C2orf47 (Chromosome 2 Open Reading Frame 47 (C2orf47))
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别名
- C2ORF47
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背景
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Synonyms: Chromosome 2 open reading frame 47, Hhypothetical protein LOC79568,
Background: C2orf47, also known as FLJ22555 or DKFZp666A212, is a 291 amino acid mitochondrial protein that is encoded by a gene located on human chromosome 2q33.1. The second largest human chromosome, chromosome 2 consists of 237 million bases, encodes over 1,400 genes and makes 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 seen in modern form today in apes.
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基因ID
- 79568
抗原
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