DENND4C 抗体
Quick Overview for DENND4C 抗体 (ABIN1387120)
抗原
适用
宿主
克隆类型
标记
应用范围
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    - 
                                            交叉反应
- 人, 小鼠, 大鼠
- 
                                            纯化方法
- Purified by Protein A.
- 
                                            免疫原
- KLH conjugated synthetic peptide derived from human DENND4C
- 
                                            亚型
- IgG
 
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    - 
                                            应用备注
- 
                        WB 1:300-5000
 IHC-P 1:200-400
 IF(IHC-P) 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
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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.
- 
                                            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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    - DENND4C (DENN/MADD Domain Containing 4C (DENND4C))
- 
                                            别名
- DENND4C
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                                            背景
- 
                        Synonyms: C9orf55, C9orf55B, DEN4C_HUMAN, DENN domain-containing protein 4C, DENN/MADD domain containing 4C, DENND4C. Background: DENND4C is a 1,673 amino acid multi-pass membrane protein. DENND4C contains a dDENN domain, DENN domain, uDENN domain and a PPR (pentatricopeptide) repeat. As a result of alternative splicing, six DENND4C isoforms exist. The gene encoding DENND4C maps to human chromosome 9, which houses over 900 genes and comprises nearly 4 % of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. 
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                                            基因ID
- 55667
 抗原
- 
                    
 
                                     
                                     
                                    