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This locus encodes an AT-rich DNA interacting domain-containing protein. Additionally we are shipping ARID1B Kits (1) and and many more products for this protein.
Showing 10 out of 39 products:
Human Polyclonal ARID1B Primary Antibody for IF, ELISA - ABIN1534011
Mungall, Palmer, Sims, Edwards, Ashurst, Wilming, Jones, Horton, Hunt, Scott, Gilbert, Clamp, Bethel, Milne, Ainscough, Almeida, Ambrose, Andrews, Ashwell, Babbage, Bagguley, Bailey, Banerjee, Barker et al.: The DNA sequence and analysis of human chromosome 6. ... in Nature 2003
Human Monoclonal ARID1B Primary Antibody for IF, IHC (p) - ABIN528194
Flores-Alcantar, Gonzalez-Sandoval, Escalante-Alcalde, Lomelí: Dynamics of expression of ARID1A and ARID1B subunits in mouse embryos and in cells during the cell cycle. in Cell and tissue research 2011
STAT3 (show STAT3 Antibodies)/Arid1b/beta-catenin (show CTNNB1 Antibodies) pathway is driving neurofibroma initiation.
The patterns of expression of ARID1A (show ARID1A Antibodies) and ARID1B genes through various mouse embryonic stages, was examined.
These data suggest that the BAF250B-associated SWI (show SMARCA1 Antibodies)/SNF (show SNRPA Antibodies) is essential for mouse embryonic stem cells to maintain their normal proliferation and pluripotency.
A subset of mammalian SWI (show SMARCA1 Antibodies)/SNF (show SNRPA Antibodies) complexes, specifically containing ARID1B, is required for efficient cell cycle re-entry and for association of activation factors with the c-myc (show MYC Antibodies) promoter.
Chromosome analysis by array-CGH revealed a small interstitial 6q deletion spanning approximately 1.1 Mb of DNA and containing only one coding gene, ARID1B. We suggest that ARID1B is the key gene behind 6q microdeletion syndrome, and we discuss its possible role in the phenotypic manifestations
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings.
ARID1B potentially serves as a valuable prognostic and predictive biomarker as well as a therapeutic target in breast cancer.
This study demonstrate that ARID1B is required for neuronal differentiation in the developing brain, such as in dendritic arborization and synapse formation.
De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature
Results show the crystal structure and binding site of SWI1 protein and identify loop L1 and L2 regions of SWI1 ARID likely play key roles in ARID-DNA interactions.
ARID1B role in genome-wide transcriptional regulation by SWI (show SMARCA1 Antibodies)/SNF (show SNRPA Antibodies) complexes.
This study provide the evidence ARID1B mutation releate to Autism Spectrum Disorder.
Chromatin-Remodeling-Factor (show ASH1L Antibodies) ARID1B Represses Wnt (show WNT2 Antibodies)/beta-Catenin (show CTNNB1 Antibodies) Signaling.
BAF (show BANF1 Antibodies) complex gene ARID1B is mutated in Coffin-Siris syndrome patients.
This locus encodes an AT-rich DNA interacting domain-containing protein. The encoded protein is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. The protein encoded by this locus is similar to AT-rich interactive domain-containing protein 1A. These two proteins function as alternative, mutually exclusive ARID-subunits of the SWI/SNF complex. The associated complexes play opposing roles. Alternatively spliced transcript variants encoding different isoforms have been described.
AT rich interactive domain 1B (Swi1 like)
, AT-rich interactive domain-containing protein 1B
, transcription factor 1
, ARID domain-containing protein 1B
, BRG1-associated factor 250b
, BRG1-binding protein ELD/OSA1
, ELD (eyelid)/OSA protein