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- 抗原 See all CCDC112 抗体
- CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))
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适用
- 人, 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 CCDC112 antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Fusion protein of human CCDC112
- 亚型
- IgG
- Top Product
- Discover our top product CCDC112 Primary Antibody
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anti-Coiled-Coil Domain Containing 112 (CCDC112) (AA 201-446) antibody
CCDC112 适用: 人 ELISA, WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 112 (CCDC112) (AA 71-120) antibodyCCDC112 适用: 人, 小鼠, 大鼠, Bat, Cow, 犬, 猴 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 112 (CCDC112) (N-Term) antibodyCCDC112 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IHC 1:40-1:200, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.5 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
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- 抗原
- CCDC112 (Coiled-Coil Domain Containing 112 (CCDC112))
- 别名
- CCDC112 (CCDC112 产品)
- 别名
- CCDC112 antibody, RGD1561942 antibody, MBC1 antibody, 8430438M01Rik antibody, AW108467 antibody, coiled-coil domain containing 112 antibody, CCDC112 antibody, Ccdc112 antibody, ccdc112 antibody
- 背景
- CCDC112 (coiled-coil domain containing 112), also known as MBC1 (mutated in bladder cancer 1), is a 446 amino acid protein. The gene encoding CCDC112 is located on chromosome 5. Due to alternative splicing events, CCDC112 exists as two isoforms. Chromosome 5 comprises about 6 % of human genomic DNA and contains 181 million base pairs encoding around 1,000 genes. It 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. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
- UniProt
- Q8NEF3
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