CCDC51 抗体 (AA 151-250) (Alexa Fluor 594)
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- 抗原 See all CCDC51 抗体
- CCDC51 (Coiled-Coil Domain Containing 51 (CCDC51))
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抗原表位
- AA 151-250
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适用
- 小鼠
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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 CCDC51 antibody is conjugated to Alexa Fluor 594
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC51
- 亚型
- IgG
- Top Product
- Discover our top product CCDC51 Primary Antibody
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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
- CCDC51 (Coiled-Coil Domain Containing 51 (CCDC51))
- 别名
- CCDC51 (CCDC51 产品)
- 别名
- 5730568A12Rik antibody, AI551049 antibody, RGD1311466 antibody, coiled-coil domain containing 51 antibody, CCDC51 antibody, Ccdc51 antibody
- 背景
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Synonyms: CCD51_HUMAN, CCDC51, Coiled-coil domain-containing protein 51, FLJ12436, RGD1311466, AI551049, 5730568A12Rik.
Background: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC51 (coiled-coil domain containing 51) is a 411 amino acid multi-pass membrane protein that exists as two alternatively spliced isoforms. The gene encoding CCDC51 maps to human chromosome 3, which is made up of about 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
- 79714
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