BRG1 (SMARCA4) (NM_001128849) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC226420L3V
- LentiORF®
Lenti ORF particles, SMARCA4 (Myc-DDK tagged) - Human SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 (SMARCA4), transcript variant 1, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Product Name | BRG1 (SMARCA4) (NM_001128849) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | BAF190; BAF190A; BRG1; CSS4; hSNF2b; MRD16; RTPS2; SNF2; SNF2-beta; SNF2L4; SNF2LB; SWI2 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001128849 |
ORF Size | 5037 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC226420).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_001128849.1 |
RefSeq ORF | 5040 bp |
Locus ID | 6597 |
Protein Families | Druggable Genome, Transcription Factors |
MW | 188 kDa |
Gene Summary | The protein encoded by this gene is a member of the SWI/SNF family of proteins and is similar to the brahma protein of Drosophila. 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. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. In addition, this protein can bind BRCA1, as well as regulate the expression of the tumorigenic protein CD44. Mutations in this gene cause rhabdoid tumor predisposition syndrome type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012] |
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