CCDC104 抗体 (AA 241-342)
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- 抗原 See all CCDC104 抗体
- CCDC104 (Coiled-Coil Domain Containing 104 (CCDC104))
- 抗原表位
- AA 241-342
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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 CCDC104 antibody is un-conjugated
- 应用范围
- ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,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 CCDC104
- 亚型
- IgG
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- 应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- CCDC104 (Coiled-Coil Domain Containing 104 (CCDC104))
- 别名
- CCDC104 (CCDC104 产品)
- 别名
- MGC76095 antibody, MGC108006 antibody, 2300003H10 antibody, 4931428D14Rik antibody, RGD1311732 antibody, zgc:136497 antibody, cilia and flagella associated protein 36 antibody, cilia and flagella associated protein 36 L homeolog antibody, cfap36 antibody, CFAP36 antibody, Cfap36 antibody, cfap36.L antibody
- 背景
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Synonyms: CC104_HUMAN, CCDC104, Coiled coil domain containing 104, Coiled-coil domain-containing protein 104, MGC15407.
Background: CCDC104 is a 342 amino acid protein that exists as two alternatively spliced isoforms. CCDC104 undergoes post-translational phosphorylation following DNA damage, most likely by either ATR or ATM. The gene encoding CCDC104 maps to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene.
- 基因ID
- 112942
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