抗人 CROCCP3 抗体对
01AB03854
Putative ciliary rootlet coiled-coil protein-like 2 (CROCCP3) is a pseudogene associated with the ciliary rootlet structure, which plays a crucial role in the organization and function of cilia in eukaryotic cells. It is believed to be involved in processes such as centriole cohesion and cilium assembly, contributing to the structural integrity of the cytoskeletal framework that supports ciliary function. It shares similarities with the CROCC gene, which encodes rootletin, an essential protein for maintaining centrosome cohesion during cell division. Research indicates that disruptions in related proteins can lead to developmental disorders such as microcephaly and Seckel syndrome, highlighting the importance of ciliary structures in cellular processes and human health.
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技术参数
- 靶点基因名
- CROCCP3
- 基因别名
- CROCCL2; KIAA1922
- 蛋白别名
- CROCC pseudogene 3; CROCCP3
- UniProt
- Q8IVE0
- 物种
- Human
产品详情
- 靶点名称
- CROCCP3
- 蛋白名称
- CROCC pseudogene 3
- 蛋白别名
- Putative ciliary rootlet coiled-coil protein-like 2 protein; Ciliary rootlet coiled-coil protein pseudogene 3
- 靶点基因名
- CROCCP3
- 基因别名
- CROCCL2; KIAA1922
- UniProt
- Q8IVE0
- 来源物种
- Homo sapiens (Human)
- 物种反应性
- Human
背景介绍
Putative ciliary rootlet coiled-coil protein-like 2 (CROCCP3) is a pseudogene associated with the ciliary rootlet structure, which plays a crucial role in the organization and function of cilia in eukaryotic cells. It is believed to be involved in processes such as centriole cohesion and cilium assembly, contributing to the structural integrity of the cytoskeletal framework that supports ciliary function. It shares similarities with the CROCC gene, which encodes rootletin, an essential protein for maintaining centrosome cohesion during cell division. Research indicates that disruptions in related proteins can lead to developmental disorders such as microcephaly and Seckel syndrome, highlighting the importance of ciliary structures in cellular processes and human health.