C2orf49 抗体 (AA 141-232) (AbBy Fluor® 647)
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- 抗原 See all C2orf49 products
- C2orf49 (Chromosome 2 Open Reading Frame 49 (C2orf49))
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抗原表位
- AA 141-232
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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 C2orf49 antibody is conjugated to AbBy Fluor® 647
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C2orf49
- 亚型
- IgG
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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
- C2orf49 (Chromosome 2 Open Reading Frame 49 (C2orf49))
- 别名
- C2orf49 (C2orf49 产品)
- 别名
- asw antibody, asw-a antibody, chromosome 11 open reading frame, human C2orf49 antibody, chromosome 2 open reading frame 49 antibody, chromosome 2 open reading frame 49 L homeolog antibody, expressed sequence AI597479 antibody, similar to expressed sequence AI597479 antibody, C11H2orf49 antibody, C2orf49 antibody, c2orf49.L antibody, AI597479 antibody, RGD1310553 antibody
- 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.
- 基因ID
- 79074
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