United States
Germany
Japan
United Kingdom
China
HBS1L (NM_006620) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC208125L3V
- LentiORF®
-
Lenti ORF particles, HBS1L (Myc-DDK tagged) - Human HBS1-like (S. cerevisiae) (HBS1L), transcript variant 1, 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 8,930.00
Product images
CNY 2,950.00
CNY 1,999.00
CNY 2,700.00
Specifications
| Product Data | |
| Product Name | HBS1L (NM_006620) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | EF-1a; eRF3c; ERFS; HBS1; HSPC276 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_006620 |
| ORF Size | 2052 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC208125).
|
| 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_006620.2 |
| RefSeq Size | 7163 bp |
| RefSeq ORF | 2055 bp |
| Locus ID | 10767 |
| Domains | GTP_EFTU, GTP_EFTU_D3, GTP_EFTU_D2 |
| MW | 75.5 kDa |
| Gene Summary | This gene encodes a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, May 2009] |
Documents
| Product Manuals |
| FAQs |
| SDS |
