- ￥880
- Bioss
- bs-16387P
- 2025年10月16日
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- 详细信息
- 技术资料
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500ug
| 产品编号 | bs-16387P |
| 英文名称 | ZZZ3 Antibody Blocking Peptide |
| 中文名称 | 锌指蛋白ZZZ3封闭多肽 |
| 英文别名 | ATAC component 1 homolog; ATAC1; DKFZp313N0119; DKFZp564I052; FLJ10362; Zinc finger ZZ domain containing 3; Zinc finger ZZ type containing 3; ZZ type zinc finger containing protein 3; ZZ-type zinc finger-containing protein 3; ZZZ 3; ZZZ3; ZZZ3_HUMAN. |
| 纯化方法 | HPLC |
| 研究领域 | Epigenetics and Nuclear Signaling > Transcription > Domain Families > Zinc Finger Epigenetics and Nuclear Signaling > Transcription > Transcription Factors |
| 亚基 | Component of the ADA2A-containing complex (ATAC), composed of CSRP2BP, KAT2A, TADA2L, TADA3L, ZZ3, MBIP, WDR5, YEATS2, CCDC101 and DR1. |
| 亚细胞定位 | Nucleus. |
| 翻译后修饰 | Phosphorylated upon DNA damage, probably by ATM or ATR. |
| 相似性 | Contains 1 HTH myb-type DNA-binding domain. Contains 1 ZZ-type zinc finger. |
| 功能 | Component of the ATAC complex, a complex with histone acetyltransferase activity on histones H3 and H4. |
| 保存条件 | Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 背景资料 | ZZZ3 (ZZ-type zinc finger-containing protein 3) is a 903 amino acid protein that contains one HTH myb-type DNA-binding domain and one ZZ-type zinc finger. Phosphorylated upon DNA damage by ATM or ATR, ZZZ3 is a subunit of the ATAC complex, which is composed of GCN5, CRP2BP, ADA3, TADA2L, DR1, CCDC101, YEATS2, WDR5 and MBIP. The ATAC complex has histone acetyltransferase activity on histones H3 and H4. ZZZ3 is expressed as four isoforms produced by alternative splicing and is encoded by a gene mapping to human chromosome 1. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. |
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ZZZ3 Antibody Blocking Peptide(bs-16387P)-500ug
￥880
