C3orf49 抗体
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- 抗原 See all C3orf49 products
- C3orf49 (Chromosome 3 Open Reading Frame 49 (C3orf49))
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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 C3orf49 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C3orf49
- 亚型
- IgG
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anti-Chromosome 3 Open Reading Frame 49 (C3orf49) (AA 1-292) antibody
C3orf49 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 3 Open Reading Frame 49 (C3orf49) (Middle Region) antibodyC3orf49 适用: 人, Cow, 犬, 马, 兔, 大鼠 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
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- C3orf49 (Chromosome 3 Open Reading Frame 49 (C3orf49))
- 别名
- C3orf49 (C3orf49 产品)
- 别名
- chromosome 3 open reading frame 49 antibody, C3orf49 antibody
- 背景
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Synonyms: chromosome 3 open reading frame 49, MGC17310, CC049_HUMAN.
Background: C3orf49 is a 292 amino acid protein encoded by a gene that maps to human chromosome 3p14.1. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.
- 基因ID
- 132200
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