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Validated All-in-One™ qPCR Primer for SMARCA1(NM_003069.4) Search again
Product ID:
HQP109946
(click here to view gene annotation page)
Species:
Human
Symbol:
Alias:
ISWI, NURF140, SNF2L, SNF2L1, SNF2LB, SNF2LT, SWI, SWI2, hSNF2L
Gene Description:
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1
Target Gene Accession:
NM_003069.4(click here to view gene page)
Estimated Delivery:
Approximately 1-3 weeks, but may vary. Please email sales@genecopoeia.com or call 301-762-0888 to confirm ETA.
Important Note:
By default, qPCR primer pairs are designed to measure the expression level of the splice variant (accession number) you selected for this gene WITHOUT consideration of other possible variants of this gene. If this gene has multiple variants, and you would like to measure the expression levels of one particular variant, multiple variants, or all variants, please contact us for a custom service project at inquiry@genecopoeia.com.
Validated result:
Summary
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.
Gene References into function
- 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
