FANCL (NM_001114636) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC225580L4V
- LentiORF®
Lenti ORF particles, FANCL (mGFP-tagged) - Human Fanconi anemia, complementation group L (FANCL), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 9,120.00
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Specifications
Product Data | |
Product Name | FANCL (NM_001114636) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | FAAP43; PHF9; POG |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001114636 |
ORF Size | 1140 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC225580).
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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_001114636.1, NP_001108108.1 |
RefSeq ORF | 1143 bp |
Locus ID | 55120 |
Protein Pathways | Ubiquitin mediated proteolysis |
MW | 43.2 kDa |
Gene Summary | This gene encodes a ubiquitin ligase that is a member of the Fanconi anemia complementation group (FANC). Members of this group are related by their assembly into a common nuclear protein complex rather than by sequence similarity. This gene encodes the protein for complementation group L that mediates monoubiquitination of FANCD2 as well as FANCI. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2018] |
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