SRA1 (NM_001035235) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC220899L2V
- LentiORF®
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Lenti ORF particles, SRA1 (mGFP-tagged) - Human steroid receptor RNA activator 1 (SRA1), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP w/ Puro
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | SRA1 |
Synonyms | pp7684; SRA; SRAP; STRAA1 |
Mammalian Cell Selection | None |
Vector | pLenti-C-mGFP |
ACCN | NM_001035235 |
ORF Size | 1991 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC220899).
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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_001035235.1, NP_001030312.2 |
RefSeq Size | 1534 bp |
RefSeq ORF | 675 bp |
Locus ID | 10011 |
UniProt ID | Q9HD15 |
Cytogenetics | 5q31.3 |
MW | 25.5 kDa |
Gene Summary | Both long non-coding and protein-coding RNAs are transcribed from this gene, and they represent alternatively spliced transcript variants. This gene was initially defined as a non-coding RNA, which is a coactivator for several nuclear receptors (NRs) and is associated with breast cancer. It has now been found that this gene is involved in the regulation of many NR and non-NR activities, including metabolism, adipogenesis and chromatin organization. The long non-coding RNA transcripts interact with a variety of proteins, including the protein encoded by this gene. The encoded protein acts as a transcriptional repressor by binding to the non-coding RNA. [provided by RefSeq, Mar 2012] |
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