PRMT7 (NM_001184824) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC230386L4V
- LentiORF®
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Lenti ORF particles, PRMT7 (mGFP-tagged)-Human protein arginine methyltransferase 7 (PRMT7), transcript variant 2, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | PRMT7 |
Synonyms | SBIDDS |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001184824 |
ORF Size | 1926 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC230386).
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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_001184824.1, NP_001171753.1 |
RefSeq ORF | 1929 |
Locus ID | 54496 |
Protein Families | Druggable Genome |
MW | 73.6 kDa |
Gene Summary | This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients. [provided by RefSeq, May 2017] |
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