MTUS1 (NM_001166393) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC230037L4V
- LentiORF®
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Lenti ORF particles, MTUS1 (mGFP-tagged) - Human microtubule associated tumor suppressor 1 (MTUS1), transcript variant 6, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK w/ Puro
AAV Particle: DDK
Product Images
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | MTUS1 |
Synonyms | ATBP; ATIP; ATIP3; ICIS; MP44; MTSG1 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001166393 |
ORF Size | 1245 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC230037).
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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_001166393.1, NP_001159865.1 |
RefSeq ORF | 1248 bp |
Locus ID | 57509 |
UniProt ID | Q9ULD2 |
Cytogenetics | 8p22 |
Protein Families | Druggable Genome, Transcription Factors, Transmembrane |
MW | 48.5 kDa |
Gene Summary | This gene encodes a protein which contains a C-terminal domain able to interact with the angiotension II (AT2) receptor and a large coiled-coil region allowing dimerization. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. One of the transcript variants has been shown to encode a mitochondrial protein that acts as a tumor suppressor and partcipates in AT2 signaling pathways. Other variants may encode nuclear or transmembrane proteins but it has not been determined whether they also participate in AT2 signaling pathways. [provided by RefSeq, Jul 2008] |
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