C3orf37 抗体 (FITC)
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- 抗原 See all C3orf37 (C3ORF37) 抗体
- C3orf37 (C3ORF37) (Chromosome 3 Open Reading Frame 37 (C3ORF37))
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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 C3orf37 antibody is conjugated to FITC
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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 C3orf37
- 亚型
- IgG
- Top Product
- Discover our top product C3ORF37 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
- C3orf37 (C3ORF37) (Chromosome 3 Open Reading Frame 37 (C3ORF37))
- 别名
- C3orf37 (C3ORF37 产品)
- 别名
- C85376 antibody, 5-hydroxymethylcytosine (hmC) binding, ES cell specific antibody, 5-hydroxymethylcytosine (hmC) binding, ES cell-specific antibody, 5-hydroxymethylcytosine (hmC) binding, ES cell-specific L homeolog antibody, Hmces antibody, HMCES antibody, hmces.L antibody
- 背景
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Synonyms: C3orf37, CC037_HUMAN, Chromosome 3 open reading frame 37, DC12, MGC111075, UPF0361 protein C3orf37.
Background: C3orf37, also known as DC12 or MGC111075, is a 354 amino acid protein encoded by a gene that maps to human chromosome 3q21.3. 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
- 56941
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