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BANP encodes a protein that binds to matrix attachment regions. Additionally we are shipping Protein BANP Antibodies (36) and Protein BANP Kits (13) and many more products for this protein.
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results reveal the complex molecular mechanism underlying SMAR1-mediated signal-dependent and -independent regulation of alternative splicing via Sam68 (show KHDRBS1 Proteins) deacetylation
SMAR1-mediated regulation of repair and apoptosis via a complex crosstalk involving Ku70 (show XRCC6 Proteins), HDAC6 (show HDAC6 Proteins) and Bax (show BAX Proteins).
Data indicate the role of SMAR1 protein in NF-kappaappa B dependent transcriptional regulation of pro-angiogenic chemokine (show CCL1 Proteins) interleukin-8 (IL-8 (show IL8 Proteins)).
indicate a crucial role for SMAR1 in restraining breast cancer cell migration and suggest the candidature of this scaffold matrix-associated (show SMARCA5 Proteins) region-binding protein as a tumor suppressor.
SMAR1 has a role in repressing c-Fos-mediated HPV18 E6 transcription through alteration of chromatin histone deacetylation
During hemin-induced erythroid differentiation, enhanced expression of SMAR1 negatively correlates with miR (show MLXIP Proteins)-320a expression.
TCF-4 (show TCF4 Proteins), beta-catenin (show CTNNB1 Proteins), and SMAR1 tether at the -143-nucleotide site on the HIV LTR to inhibit HIV promoter activity.
Results indicate that SMAR1 is an important player in p300 (show EP300 Proteins)-p53 (show TP53 Proteins) regulated DNA damage signalling pathway and can exert its effect on apoptosis in a transcription independent manner.
multiple roles of nuclear matrix associated (show SMARCA5 Proteins) protein SMAR1 in regulating various cellular target genes involved in cell growth, apoptosis and tumorigenesis.(REVIEW)
A novel mechanism of regulation of oxidative stress by ATM (show ATM Proteins) through modulation of SMAR1-AKR1a4 complex, is proposed.
we report an essential role of the matrix attachment region (MAR)-binding protein SMAR1 in regulating immune response during allergic airway disease
SMAR1, a known transcription factor and tumor suppressor, is directly involved in maintaining regulatory T cell fate decision
Glucose deprivation can induce p53 (show TP53 Proteins) internal ribosome entry sites (IRESs) and also increases cytoplasmic abundance of SMAR1 that in turn binds to p53 (show TP53 Proteins) IRESs, indicating the role of SMAR1 in controlling translation of p53 (show TP53 Proteins) isoforms.
combined action of Foxp3 (show FOXP3 Proteins) and SMAR1 restricts effector cytokine production and enhance the production of IL-10 (show IL10 Proteins) by colonic Treg cells that controls acute colitis
SMAR1 and p53 (show TP53 Proteins) act synergistically to up-regulate GAD65 (show GAD2 Proteins) expression upon Streptozotocin treatment.
C/EBPbeta (show CEBPB Proteins) may regulate preadipocyte proliferation through activation of banp and trim35 (show TRIM35 Proteins).
TNFalpha (show TNF Proteins) mediated regulation of CD40 (show CD40 Proteins) expression occurs by dual phosphorylation of SMAR1 and STAT1 (show STAT1 Proteins).
SMAR1 modulates the roughness of cell surface.
SMAR1-mediated stabilization of p53 (show TP53 Proteins) is brought about by inhibiting Mdm2 (show MDM2 Proteins)-mediated degradation of p53 (show TP53 Proteins)
This gene encodes a protein that binds to matrix attachment regions. The protein forms a complex with p53 and negatively regulates p53 transcription, and functions as a tumor suppressor and cell cycle regulator. Multiple transcript variants encoding different isoforms have been found for this gene.
, BTG3 associated nuclear protein
, BEN domain-containing protein 1
, scaffold/matrix-associated region-1-binding protein
, btg3-associated nuclear protein