RGS6 (NM_004296) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC211189L4V
- LentiORF®
-
Lenti ORF particles, RGS6 (mGFP-tagged) - Human regulator of G-protein signaling 6 (RGS6), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 9,975.00
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Specifications
Product Data | |
Product Name | RGS6 (NM_004296) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | GAP; HA117; S914 |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_004296 |
ORF Size | 1416 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC211189).
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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_004296.3 |
RefSeq Size | 5750 bp |
RefSeq ORF | 1419 bp |
Locus ID | 9628 |
Domains | RGS, DEP, G-gamma |
Protein Families | Druggable Genome |
MW | 54.4 kDa |
Gene Summary | This gene encodes a member of the RGS (regulator of G protein signaling) family of proteins, which are defined by the presence of a RGS domain that confers the GTPase-activating activity of these proteins toward certain G alpha subunits. This protein also belongs to a subfamily of RGS proteins characterized by the presence of DEP and GGL domains, the latter a G beta 5-interacting domain. The RGS proteins negatively regulate G protein signaling, and may modulate neuronal, cardiovascular, lymphocytic activities, and cancer risk. Many alternatively spliced transcript variants encoding different isoforms with long or short N-terminal domains, complete or incomplete GGL domains, and distinct C-terminal domains, have been described for this gene, however, the full-length nature of some of these variants is not known.[provided by RefSeq, Mar 2011] |
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