CCDC69 抗体 (AA 41-140) (AbBy Fluor® 555)
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北京 101111
Quick Overview for CCDC69 抗体 (AA 41-140) (AbBy Fluor® 555) (ABIN888081)
抗原
See all CCDC69 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 41-140
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交叉反应
- 人
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预测反应
- Dog,Cow,Sheep,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human CCDC69
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亚型
- IgG
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anti-Coiled-Coil Domain Containing 69 (CCDC69) (AA 1-296) antibody
CCDC69 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4G6 unconjugated
anti-Coiled-Coil Domain Containing 69 (CCDC69) (AA 41-140) antibodyCCDC69 适用: 人 ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 69 (CCDC69) (C-Term) antibodyCCDC69 适用: 人, Cow, 豚鼠, 猴, 兔 WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 69 (CCDC69) (Middle Region) antibodyCCDC69 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 69 (CCDC69) (Middle Region) antibodyCCDC69 适用: 人, 大鼠, Cow, 豚鼠, 犬, 马, Pig WB 宿主: 兔 Polyclonal unconjugated
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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
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- CCDC69 (Coiled-Coil Domain Containing 69 (CCDC69))
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别名
- CCDC69
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背景
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Synonyms: CCD69_HUMAN, ccdc69, Coiled coil domain containing 69, Coiled-coil domain-containing protein 69.
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. CCDC69 (Coiled-coil domain-containing protein 69) is a 296 amino acid protein that is encoded by a gene which maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6 % of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
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基因ID
- 26112
抗原
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