United States
Germany
Japan
United Kingdom
China
alpha Sarcoglycan (SGCA) (NM_000023) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC206577L4V
- LentiORF®
-
Lenti ORF particles, SGCA (mGFP-tagged) - Human sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein) (SGCA), transcript variant 1, 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 9,975.00
货期*
详询
规格
Product images
经常一起买 (3)
Specifications
| Product Data | |
| Product Name | alpha Sarcoglycan (SGCA) (NM_000023) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | 50DAG; adhalin; ADL; DAG2; DMDA2; LGMD2D; LGMDR3; SCARMD1 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_000023 |
| ORF Size | 1161 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC206577).
|
| 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_000023.1 |
| RefSeq Size | 1441 bp |
| RefSeq ORF | 1164 bp |
| Locus ID | 6442 |
| Protein Families | Druggable Genome, Transmembrane |
| Protein Pathways | Arrhythmogenic right ventricular cardiomyopathy (ARVC), Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM), Viral myocarditis |
| MW | 42.9 kDa |
| Gene Summary | This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008] |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
You may also need
其它alpha Sarcoglycan产品
Customer
Reviews
Loading...
