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SMARCAD1 encodes a member of the SNF subfamily of helicase proteins. De plus, nous expédions SWI/SNF-Related, Matrix-Associated Actin-Dependent Regulator of Chromatin, Subfamily A, Containing DEAD/H Box 1 Protéines (4) et beaucoup plus de produits pour cette protéine.
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Human Polyclonal SMARCAD1 Primary Antibody pour IP, WB - ABIN256707
Chakraborty, Pandita, Hambarde, Mattoo, Charaka, Ahmed, Iyer, Hunt, Pandita: SMARCAD1 Phosphorylation and Ubiquitination Are Required for Resection during DNA Double-Strand Break Repair. dans iScience 2018
SMARCAD1 knockdown resulted in a significant decrease in breast cancer cell proliferation and colony formation, leading to the significant inhibition of tumour growth in both the chick embryo and nude mouse xenograft models. This inhibition was due, at least in part, to a decrease in IKKbeta (Montrer IKBKB Anticorps) expression.
identifies Smarcad1/Fun30 as an accessory factor for the mismatch repair reaction
A splice variant (c.378+1G>T) in the SMARCAD1 gene co-segregated with Basan syndrome in a large Chinese family.
These results indicate that SMARCAD1 is involved in breast cancer metastasis
BRCA1-BARD1 (Montrer BARD1 Anticorps) ligase activity and subsequent SMARCAD1-dependent chromatin remodeling are critical regulators of DNA repair in cancer cells.
These data indicate a pivotal role for the SMARCAD1-skin specific isoform in dermatoglyph formation, ADG and epidermal differientation gene expression
findings unveil an evolutionarily conserved role for the Fun30 and SMARCAD1 chromatin remodellers in controlling end resection, homologous recombination and genome stability in the context of chromatin
The existence of a short isoform of SMARCAD1 exclusively expressed in the skin, is demonstrated.
Findings suggest that chromatin remodeling by SMARCAD1 ensures that silenced loci, such as pericentric heterochromatin, are correctly perpetuated.
Results suggest a novel model for gene regulation via the SMARCAD1/KIAA1122 protein complex.
These data suggest a model in which SMARCAD1 regulates naive pluripotency by interacting with H3 arginine 26 citrullination and suppressing heterochromatin formation.
This gene encodes a member of the SNF subfamily of helicase proteins. The encoded protein plays a critical role in the restoration of heterochromatin organization and propagation of epigenetic patterns following DNA replication by mediating histone H3/H4 deacetylation. Mutations in this gene are associated with adermatoglyphia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
, SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1
, SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1-like
, SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1A
, ATP-dependent helicase 1
, ATP-dependent helicase SMARCAD1
, enhancer trap locus 1
, enhancer trap locus homolog 1