United States
Germany
Japan
United Kingdom
China
RAD50 (NM_005732) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC211751L3V
- LentiORF®
-
Lenti ORF particles, RAD50 (Myc-DDK-tagged)-Human RAD50 homolog (S. cerevisiae) (RAD50), 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 11,210.00
货期*
详询
规格
Product images
经常一起买 (3)
Specifications
| Product Data | |
| Product Name | RAD50 (NM_005732) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | hRad50; NBSLD; RAD502 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_005732 |
| ORF Size | 3936 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC211751).
|
| 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_005732.3 |
| RefSeq Size | 6597 bp |
| RefSeq ORF | 3939 bp |
| Locus ID | 10111 |
| Domains | Rad50_zn_hook |
| Protein Families | Druggable Genome |
| Protein Pathways | Homologous recombination, Non-homologous end-joining |
| MW | 154.3 kDa |
| Gene Summary | The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Rad50, a protein involved in DNA double-strand break repair. This protein forms a complex with MRE11 and NBS1. The protein complex binds to DNA and displays numerous enzymatic activities that are required for nonhomologous joining of DNA ends. This protein, cooperating with its partners, is important for DNA double-strand break repair, cell cycle checkpoint activation, telomere maintenance, and meiotic recombination. Knockout studies of the mouse homolog suggest this gene is essential for cell growth and viability. Mutations in this gene are the cause of Nijmegen breakage syndrome-like disorder.[provided by RefSeq, Apr 2010] |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
You may also need
Customer
Reviews
Loading...
