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BANP encodes a protein that binds to matrix attachment regions.
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Cdc20 (show CDC20 ELISA Kits) functions as an important negative regulator of SMAR1 in higher grades of cancer
Dysregulated circ-BANP appears to have an important role in colorectal cancer cells.
results reveal the complex molecular mechanism underlying SMAR1-mediated signal-dependent and -independent regulation of alternative splicing via Sam68 (show KHDRBS1 ELISA Kits) deacetylation
SMAR1-mediated regulation of repair and apoptosis via a complex crosstalk involving Ku70 (show XRCC6 ELISA Kits), HDAC6 (show HDAC6 ELISA Kits) and Bax (show BAX ELISA Kits).
Data indicate the role of SMAR1 protein in NF-kappaappa B dependent transcriptional regulation of pro-angiogenic chemokine (show CCL1 ELISA Kits) interleukin-8 (IL-8 (show IL8 ELISA Kits)).
indicate a crucial role for SMAR1 in restraining breast cancer cell migration and suggest the candidature of this scaffold matrix-associated 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 ELISA Kits)-320a expression.
TCF-4 (show TCF4 ELISA Kits), beta-catenin (show CTNNB1 ELISA Kits), 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 ELISA Kits)-p53 (show TP53 ELISA Kits) regulated DNA damage signalling pathway and can exert its effect on apoptosis in a transcription independent manner.
SMAR1 transgenic mice exhibited susceptibility to M. tuberculosis infection in vivo irrespective of genetic background. This susceptibility was attributed to downregulation of Th1 (show HAND1 ELISA Kits) response and its hallmark cytokine IFN-gamma (show IFNG ELISA Kits)
This study reveals a critical role of SMAR1 in maintaining the proinflammatory immune responses by repressing Th1 (show HAND1 ELISA Kits) and Th17 cell function and it gives the novel insight into immune regulatory mechanisms.
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 ELISA Kits) internal ribosome entry sites (IRESs) and also increases cytoplasmic abundance of SMAR1 that in turn binds to p53 (show TP53 ELISA Kits) IRESs, indicating the role of SMAR1 in controlling translation of p53 (show TP53 ELISA Kits) isoforms.
combined action of Foxp3 (show FOXP3 ELISA Kits) and SMAR1 restricts effector cytokine production and enhance the production of IL-10 (show IL10 ELISA Kits) by colonic Treg cells that controls acute colitis
SMAR1 and p53 (show TP53 ELISA Kits) act synergistically to up-regulate GAD65 (show GAD2 ELISA Kits) expression upon Streptozotocin treatment.
A novel mechanism of regulation of oxidative stress by ATM (show ATM ELISA Kits) through modulation of SMAR1-AKR1a4 complex, is proposed.
C/EBPbeta may regulate preadipocyte proliferation through activation of banp and trim35.
TNFalpha (show TNF ELISA Kits) mediated regulation of CD40 (show CD40 ELISA Kits) expression occurs by dual phosphorylation of SMAR1 and STAT1 (show STAT1 ELISA Kits).
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