CCDC83 抗体 (AA 101-200) (AbBy Fluor® 750)
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- 抗原 See all CCDC83 抗体
- CCDC83 (Coiled-Coil Domain Containing 83 (CCDC83))
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抗原表位
- AA 101-200
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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 CCDC83 antibody is conjugated to AbBy Fluor® 750
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应用范围
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC83
- 亚型
- IgG
- Top Product
- Discover our top product CCDC83 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
- CCDC83 (Coiled-Coil Domain Containing 83 (CCDC83))
- 别名
- CCDC83 (CCDC83 产品)
- 别名
- 4930549K11Rik antibody, 4930554C01Rik antibody, 4932423M01Rik antibody, coiled-coil domain containing 83 antibody, CCDC83 antibody, Ccdc83 antibody
- 背景
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Synonyms: Coiled coil domain containing 83, Coiled coil domain containing protein 83, HSD9, QtsA 10152, QtsA 19320, CCD83_HUMAN.
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. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
- 基因ID
- 220047
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