ST3GAL5 (NM_001042437) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC211663L3V
- LentiORF®
Lenti ORF particles, ST3GAL5 (Myc-DDK-tagged)-Human ST3 beta-galactoside alpha-2,3-sialyltransferase 5 (ST3GAL5), transcript variant 2, 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 8,265.00
货期*
详询
规格
Product images
经常一起买 (3)
Specifications
Product Data | |
Product Name | ST3GAL5 (NM_001042437) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | SATI; SIAT9; SIATGM3S; SPDRS; ST3Gal V; ST3GalV |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001042437 |
ORF Size | 1185 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC211663).
|
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_001042437.1 |
RefSeq Size | 2262 bp |
RefSeq ORF | 1188 bp |
Locus ID | 8869 |
Protein Families | Transmembrane |
Protein Pathways | Glycosphingolipid biosynthesis - ganglio series, Metabolic pathways |
MW | 45.4 kDa |
Gene Summary | Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Documents
Product Manuals |
FAQs |
SDS |
Resources
You may also need
其它ST3GAL5产品
Customer
Reviews
Loading...