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The gene variously symbolized ALL1, HRX, or MLL located on 11q23 has been demonstrated to be fused with a number of translocation partners in cases of leukemia. 再加上，我们可以发MLLT11 蛋白 (8)和数多这个蛋白质的别的产品。
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Human Monoclonal MLLT11 Primary Antibody for ELISA, WB - ABIN564754
Chang, Li, Hou, Wu, Lu, Di, Jin, Ou, Shen, Shao: Identification of the functional role of AF1Q in the progression of breast cancer. in Breast cancer research and treatment 2008
Show all 5 Pubmed References
AF1q was up-regulated in human colorectal cancer tissues, and that this up-regulation was associated with tumor metastasis. AF1q contributes to CRC (显示 CALR 抗体) tumorigenesis through the activation of the AKT (显示 AKT1 抗体) signaling pathway.
Data show that MLLT11/AF1q-induced PDGFR (显示 PDGFRB 抗体) signaling enhanced STAT3 (显示 STAT3 抗体) activity through Src kinase (显示 CSK 抗体) activation.
AF1q was significantly lower in borderline ovarian tumors (i.e., tumors of low malignant potential without stromal invasion) than in invasive tumors, thus corroborating the association between high AF1q expression and increased migratory/invasive cell behavior and confirming its potential role in ovarian cancer progression.
These results suggest that AF1q would have a role as an enhancer in generation of stem-like population through activation of Wnt (显示 WNT2 抗体) signaling pathway.
Findings indicate that breast cancer cells with a hyperactive AF1q/TCF7 (显示 TCF7 抗体)/CD44 (显示 CD44 抗体) regulatory axis in the primary sites may represent "metastatic founder cells" which have invasive properties.
Results demonstrate that AF1q gene transcription is regulated by REST through direct binding at -383 to -363 bp of AF1q promoter.
AF1Q had a KFERQ-like motif.
AF1q plays a role in the onset of basal apoptosis in ovarian cancer cells, thus providing new information about the activity of this protein whose biologic functions are mostly unknown
Using in vitro assays based on either forced expression or shRNA-mediated silencing of AF1q, the study provides evidence that the protein promotes T- over B-cell differentiation in multipotent hematopoietic progenitors.
AF1q up-regulation of BAD is through its effect on NF-kappaB (显示 NFKB1 抗体) and this may hint of its oncogenic mechanism in cancer.
MLLT11 is a pan (显示 SUPT6H 抗体)-neuronal marker, suggesting a role in neural differentiation in the central nervous system and neural crest-cell derived peripheral ganglia
The mouse Af1q, homologue of human AF1q, was found to be significantly up-regulated during the neuronal production from neural stem cells
The gene variously symbolized ALL1, HRX, or MLL located on 11q23 has been demonstrated to be fused with a number of translocation partners in cases of leukemia. t(1\;11)(q21\;q23) translocations that fused the MLL gene to a gene on chromosomal band 1q21 in 2 infants with acute myelomonocytic leukemia have been demonstrated. The N-terminal portion of the MLL gene is critical for leukemogenesis in translocations involving band 11q23. This gene encodes 90 amino acids. It was found to be highly expressed in the thymus but not in peripheral lymphoid tissues. In contrast to its restricted distribution in normal hematopoietic tissue, this gene was expressed in all leukemic cell lines tested.
, ALL1 fused gene from chromosome 1q
, ALL1-fused gene from chromosome 1q
, zinc finger protein 692
, AF1Q protein