产品货号:
Z29906
中文名称:
WDR35抗体
英文名称:
Anti-WDR35 Antibody
产品规格:
0.1mg
发货周期:
1~3天
产品价格:
询价
抗体名称 | Anti-WDR35 Antibody |
指标别名 | CED2,IFTA1,SRTD7,IFT121,KIAA1336,WD repeat-containing protein 35,Intraflagellar transport protein 121 homolog |
克隆性 | Polyclonal |
检验物种 | human |
应用范围 | ELISA,IHC |
基因名称 | WDR35 |
抗体来源 | Rabbit |
抗体类型 | IgG |
免疫原 | WDR35 antibody was raised against a 16 amino acid synthetic peptide near the amino terminus of human WDR35.The immunogen is located within amino acids 60 - 110 of WDR35. |
计算分子量 | 134kDa |
成分 | WDR35 Antibody is supplied in PBS containing 0.02% sodium azide. |
纯化方式 | WDR35 Antibody is affinity chromatography purified via peptide column. |
浓度 | 1mg/mL |
产品形态 | 溶液 |
保存条件 | 4℃可保存3个月,-20℃可保存1年。 |
背景资料 | WD40 repeats are a common structural module in eukaryotic proteins,and proteins containing WD40 domains have a wide range of functions,including signal transduction,cell cycle regulation,RNA splicing,and transcription.One such protein,WDR35,also known as CED2,has been shown to be mutated in patients with Sensenbrenner syndrome/cranioectodermal dysplasia (CED),an autosomal-recessive disease that is characterized by craniosynstosis and ectodermal and skeletal abnormalities.WDR35 localizes to cilia and dentrosomes during embryogenesis and human and mouse fibroblasts that lack this gene fail to produce cilia.Mutations in this gene can also cause short-rib polydactyly syndromes due to abnormal ciliogenesis. |
Uniprot ID | Q9P2L0 |
基因名全称 | WD repeat domain 35 |
蛋白名全称 | WD repeat domain 35 |
推荐稀释比 | WDR35 antibody can be used for detection of WDR35 by immunohistochemistry at 5μg/mL.Antibody validated:Immunohistochemistry in human samples.All other applications and species not yet tested. |
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