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Human Monoclonal SMARCA1 Primary Antibody for IHC, WB - ABIN2668290
Eckey, Kuphal, Straub, Rümmele, Kremmer, Bosserhoff, Becker: Nucleosome remodeler SNF2L suppresses cell proliferation and migration and attenuates Wnt signaling. in Molecular and cellular biology 2012
Show all 2 Pubmed References
These results begin to establish a role for SNF2L in the precise coordination of gene expression in granulosa cells during folliculogenesis and its broader implications in fertility.
Cancers are sensitive to SNF2L knockdown because, unlike their normal counterparts, they lack sufficient compensation from other family members.
The imitation switch protein SNF2L regulates steroidogenic acute regulatory protein expression during terminal differentiation of ovarian granulosa cells.
Data identified SMARCA1 as an interactive protein of DLEU1 in colorectal cancer to regulate cancer cell proliferation.
In one family, four siblings with a psychotic illness and their unaffected mother each carry a novel private missense variant in the SMARCA1 gene on the X chromosome.
Depletion of a chromatin remodeler, SMARCA1, in cancer cell lines promoted their growth.
The results suggest that the cAMP-response element consensus sequence in the SNF2L proximal promoter most likely confers constitutive activation and regulation by cAMP in neural cells.
The effect of SNF2L depletion on gene expression portray the cell in a state of activated Wnt signaling with increased proliferation and locomotion. High levels of SNF2L expression in normal melanocytes contrast with undetectable expression in melanoma.
expression profiling analyses revealed that SWI/SNF likely antagonizes Polycomb repressive complex 2, implicating this as one possible mechanism of tumor suppression
ISWI proteins Snf2H, Snf2L as well as Acf1 accumulate at UV-induced DNA damage sites within tens of seconds and reach a plateau after a few minutes.
a neuronal SNF2L variant inactivates chromatin remodeling
Brahma and Brahma/SWI2-related gene 1 have roles in hypoxic induction of the erythropoietin gene
This study provides the first insight into the mechanisms that control basal expression of human SNF2L gene.
SNF2L mutations are not a cause of X-linked mental retardation in our cohort of patients, although we cannot exclude the possibility that regulatory mutations might exist
This gene encodes a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1
, SNF2L-like protein
, SWI/SNF-related matrix-associated actin-dependent regulator of chromatin a1-like
, probable global transcription activator SNF2L1-like
, ATP-dependent helicase SMARCA1
, DNA-dependent ATPase SNF2L
, SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 1
, nucleosome-remodeling factor subunit SNF2L
, probable global transcription activator SNF2L1
, SNF2-like 1
, SWI/SNF-related matrix-associated actin-dependent regulator of chromatin a1
, global transcription activator homologous sequence
, sucrose nonfermenting 2-like protein 1