C2orf49 抗体 (AA 141-232) (HRP)
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北京 101111
Quick Overview for C2orf49 抗体 (AA 141-232) (HRP) (ABIN1712017)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 141-232
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预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Horse
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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 C2orf49
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亚型
- IgG
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anti-Chromosome 2 Open Reading Frame 49 (C2orf49) (AA 62-90), (N-Term) antibody
C2orf49 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB26338 unconjugated
anti-Chromosome 2 Open Reading Frame 49 (C2orf49) (AA 1-232) antibodyC2orf49 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 2 Open Reading Frame 49 (C2orf49) (AA 93-142) antibodyC2orf49 适用: 人 WB 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
IHC-F 1:100-500 -
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
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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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注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- C2orf49 (Chromosome 2 Open Reading Frame 49 (C2orf49))
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别名
- C2orf49
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背景
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Synonyms: Ashwin, asw, Chromosome 2 open reading frame 49, FLJ45759, MGC5509, ASHWN_HUMAN.
Background: C2orf49 (chromosome 2 open reading frame 49), also known as asw, Ashwin, MGC5509 or FLJ45759, is a 232 amino acid member of the ashwin family and is encoded by a gene located on human chromosome 2q12.2. The second largest human chromosome, chromosome 2 consists of 237 million bases encoding over 1,400 genes and 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 seen in modern form today in apes.
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基因ID
- 79074
抗原
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