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NAB2 encodes a member of the family of NGFI-A binding (NAB) proteins, which function in the nucleus to repress transcription induced by some members of the EGR (early growth response) family of transactivators. Additionally we are shipping NGFI-A Binding Protein 2 (EGR1 Binding Protein 2) Antibodies (92) and NGFI-A Binding Protein 2 (EGR1 Binding Protein 2) Proteins (5) and many more products for this protein.
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Data suggest that histone deacetylase (show HDAC1 ELISA Kits) inhibitors inhibit the induction of NGF1A-binding protein (show NAB1 ELISA Kits) Nab2 by brain derived neurotrophic factor (BDNF (show BDNF ELISA Kits)), and thereby the relative induction of dopamine and cyclic AMP-regulated phosphoprotein (show ARPP21 ELISA Kits), 32 kDa (DARPP-32 (show PPP1R1B ELISA Kits)).
Nab2 is a novel endogenous negative regulator of Egr-1 (show EGR1 ELISA Kits)-dependent TGF-beta (show TGFB1 ELISA Kits) signaling responsible for setting the intensity of fibrotic responses
Nab1 and Nab2 proteins are necessary for Schwann cells to exit the cell cycle, downregulate suppressed cAMP-inducible protein (SCIP) expression and upregulate expression of critical myelination genes.
repression of the endogenous Rad gene by NAB2 involves interaction with the CHD4 (chromodomain helicase DNA-binding protein 4 (show CHD4 ELISA Kits)) subunit of the NuRD (nucleosome remodeling and deacetylase) chromatin remodeling complex
NAB2 enhances IL-2 (show IL2 ELISA Kits) transcription by acting as a coactivator for Egr-1 (show EGR1 ELISA Kits).NAB2 is recruited to the Egr-1 (show EGR1 ELISA Kits) binding site of the IL-2 (show IL2 ELISA Kits) promoter.
We report here, that FGF23 (show FGF23 ELISA Kits) induces not only Egr-1 (show EGR1 ELISA Kits) but also two isoforms of NAB2, which are specific co-repressors of Egr-1 (show EGR1 ELISA Kits).
We delineate the common and rare NAB2-STAT6 (show STAT6 ELISA Kits) fusion variants in solitary fibrous tumors
This study confirms that meningeal Meningeal solitary fibrous tumor and hemangiopericytoma represent a histopathologic continuum linked by STAT6 (show STAT6 ELISA Kits) nuclear expression and NAB2-STAT6 (show STAT6 ELISA Kits) fusion similar to their soft tissue counterparts.
This study validated the existence of the NAB2-STAT6 (show STAT6 ELISA Kits) fusion gene in solitary fibrous tumors and examined its relation with pathological features.
also identified NAB2-STAT6 (show STAT6 ELISA Kits) fusions in two hemangiopericytomas diagnosed in the past with a common variant of NAB2ex6-STAT6ex16/17
There was no association between solitary fibrous tumors with either NAB2 exon 4-STAT6 (show STAT6 ELISA Kits) exon 2 or 3 fusion and tumors with other fusions regarding the frequency of mutations in the examined genes (P = .201).
reverse transcriptase PCR analysis identified a nerve growth factor inducible-A binding protein 2-STAT6 (show STAT6 ELISA Kits) gene fusion. Our case supports the utility of STAT6 (show STAT6 ELISA Kits) immunohistochemistry as an adjunct in the diagnosis of soft-tissue SFT (show UBE2D1 ELISA Kits) with loss of CD34 (show CD34 ELISA Kits) positivity
44 SFTs were studied to identify pathogenetically important genetic rearrangements. RT-PCR analysis identified a NAB2/STAT6 (show STAT6 ELISA Kits) fusion in 37/41 cases.
Meningeal hemangiopericytoma and solitary fibrous tumors carry the NAB2-STAT6 (show STAT6 ELISA Kits) fusion
NAB2 and EGR-1 (show EGR1 ELISA Kits) exert opposite roles in regulating TRAIL expression in human Natural Killer cells.
A gene fusion of the transcriptional repressor NAB2 with the transcriptional activator STAT6 (show STAT6 ELISA Kits) is the defining driver mutation of solitary fibrous tumor.
This gene encodes a member of the family of NGFI-A binding (NAB) proteins, which function in the nucleus to repress transcription induced by some members of the EGR (early growth response) family of transactivators. NAB proteins can homo- or hetero-multimerize with other EGR or NAB proteins through a conserved N-terminal domain, and repress transcription through two partially redundant C-terminal domains. Transcriptional repression by the encoded protein is mediated in part by interactions with the nucleosome remodeling and deactylase (NuRD) complex. Alternatively spliced transcript variants have been described, but their biological validity has not been determined.
NGFI-A binding protein 2 (EGR1 binding protein 2)
, EGR-1-binding protein 2
, NGFI-A binding protein 2 (EGR-1 binding protein 2)
, NGFI-A-binding protein 2
, EGR1 binding protein 2
, melanoma-associated delayed early response protein