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BTG1 is a member of an anti-proliferative gene family that regulates cell growth and differentiation. Additionally we are shipping BTG1 Antibodies (54) and BTG1 Proteins (6) and many more products for this protein.
BTG1 overexpression or knockdown improved or impaired insulin (show INS ELISA Kits) signaling respectively.
Btg1 regulates the proliferation of cerebellar granule precursors selectively through cyclin D1 (show CCND1 ELISA Kits).
these data show that both Btg1 and Btg2 (show BTG2 ELISA Kits) are required for normal vertebral patterning of the axial skeleton, but each gene contributes differently in specifying the identity along the anterior-posterior axis of the skeleton.
Btg1 gain- and loss-of-function experiments were consistent with the pattern of expression of this gene in the developing digits. We detected a negative influence of BTG1 in the progress of cartilage maturation and a positive influence in the formation of fibrogenic tissue.
Antiproliferative BTG1 may participate in the activation-induced cell death of microglia by lowering the threshold for apoptosis.
BTG1 interacts with ATF4 (show ATF4 ELISA Kits) and positively modulates its activity by recruiting the protein arginine methyl transferase PRMT1 (show PRMT1 ELISA Kits) to methylate ATF4 (show ATF4 ELISA Kits) on arginine residue 239.
our data suggest that BTG1 overexpression combined with radiation therapy increases the therapeutic efficacy of breast cancer treatment via regulation of the cell cycle and apoptosis-related signaling pathways.
Suggest that down-regulated BTG1 expression might promote gastric carcinogenesis partially due to its promoter methylation. BTG1 overexpression might reverse the aggressive phenotypes.
Reduced BTG1 expression is associated with increased nasopharyngeal cancer severity, suggesting it is a negative regulator of the cancer and can serve as a prognostic indicator. Reduced BTG1 expression is possibly associated with tumour metastasis.
Our results indicate that altered BTG1 expression might affect hepatocarcinogenesis and may represent a novel biomarker for HCC (show FAM126A ELISA Kits) carcinogenesis and progression.
Data indicate that microRNA-19a regulates prostate cancer cells by directly targeting B cell translocation gene-1 protein BTG1.
Altered expression of BTG1 is a potential biomarker for carcinogenesis and progression of gastric cancer, particularly for proximal nondiffuse and diffuse GC.
Results show that reduced BTG1 expression is associated with increased disease severity, suggesting it as negative regulator of thyroid cancer.
Down-regulation of BTG1 by miR (show MLXIP ELISA Kits)-454-3p renders tumor cells sensitive to radiation.
BTG1 protein levels were significantly reduced in hepatocellular cancer and were associated with lymph node metastasis, clinical stage, cell differentiation, and prognosis.
BTG1 may play an important role in the process of angiogenesis
This gene is a member of an anti-proliferative gene family that regulates cell growth and differentiation. Expression of this gene is highest in the G0/G1 phases of the cell cycle and downregulated when cells progressed through G1. The encoded protein interacts with several nuclear receptors, and functions as a coactivator of cell differentiation. This locus has been shown to be involved in a t(8\;12)(q24\;q22) chromosomal translocation in a case of B-cell chronic lymphocytic leukemia.
, BTG1 protein
, protein BTG1-like
, B-cell translocation gene 1 protein
, B-cell translocation gene 1, anti-proliferative
, anti-proliferative factor
, myocardial vascular inhibition factor
, B-cell translocation protein 1