research use only
Cat.No.: F8896
| Dilution |
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| Application |
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| WB, IP, ChIP |
| Reactivity |
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| Human, Mouse, Rat, Monkey |
| Source |
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| Rabbit Monoclonal Antibody |
| Storage Buffer |
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| PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3 |
| Storage (from the date of receipt) |
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| -20°C (avoid freeze-thaw cycles), 2 years |
| Predicted MW |
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| 65 kDa |
| Positive Control | NCCIT cells; A549 cells; NIH/3T3 cells; H-4-II-E cells; COS-7 cells |
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| Negative Control |
| Specificity |
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| CBX8 Antibody [E24E8] detects endogenous levels of total CBX8 protein. |
| Clone |
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| E24E8 |
| Synonym(s) |
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| Chromobox protein homolog 8; Polycomb 3 homolog (Pc3; hPc3); Rectachrome 1; CBX8; PC3; RC1 |
| Background |
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| CBX8, or Chromobox protein homolog 8, is a member of the CBX family within the Polycomb Repressive Complex 1 (PRC1), partnering with proteins like RING1 and BMI1 to maintain heritable gene silencing during development and stem cell self-renewal. As a canonical H3K27me3 reader, CBX8 recruits PRC1 to specific chromatin regions, ensuring stable transcriptional repression. CBX8 contains an N-terminal chromodomain that forms an aromatic cage for H3K27me3 binding, an AT-hook motif that interacts with the DNA minor groove, and a C-terminal region responsible for PRC1 assembly and localization to Polycomb group (PcG) bodies in the nucleus. Its primary functions revolve around dynamic chromatin repression: CBX8 binds to H3K27me3-marked loci, compacts chromatin through multivalent PRC1 interactions, and ubiquitinates histone H2AK119 to inhibit RNA polymerase II progression. During embryonic stem cell differentiation, CBX8 facilitates the transition from PRC1-CBX7 to PRC1-CBX8, thereby supporting the robust activation of lineage-specific genes, such as the Hox clusters. CBX8 modulates repression of the INK4A-ARF locus to enable cells to bypass oncogene-induced senescence, promotes proliferation by derepressing cyclin genes, and colocalizes with BMI1 and RING1B in nuclear PcG bodies. Disease relevance includes its role in MLL-AF9 leukemia, where CBX8 is essential for HOX gene maintenance, its involvement in fibroblast immortalization, and its influence on hematopoietic stem cell self-renewal, with overexpression driving senescence bypass and knockdown leading to G1 arrest. |
| References |
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