Fancl (NM_025923) Mouse Tagged ORF Clone Lentiviral Particle
CAT#: MR222128L4V
- LentiORF®
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Lenti ORF particles, Fancl (GFP-tagged) - Mouse Fanconi anemia, complementation group L (Fancl), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK w/ Puro
AAV Particle: DDK
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Product Images
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Specifications
Product Data | |
Type | Mouse Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | Fancl |
Synonyms | 2010322C19Rik; AW554273; B230118H11Rik; gcd; P; Phf; Phf9; Pog |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_025923 |
ORF Size | 1125 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(MR222128).
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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_025923.2 |
RefSeq Size | 1798 bp |
RefSeq ORF | 1128 bp |
Locus ID | 67030 |
UniProt ID | Q9CR14 |
Cytogenetics | 11 A3.3 |
Gene Summary | This gene encodes the complementation group L subunit of the multimeric Fanconi anemia (FA) nuclear complex composed of proteins encoded by over ten Fanconi anemia complementation (FANC) group genes. The FA complex is necessary for protection against DNA damage. This gene product, an E3 ubiquitin ligase, catalyzes and is required for the monoubiquitination of the protein encoded by the Fanconi anemia, complementation group D2 gene, a critical step in the FA pathway (PMID: 12973351, 21229326). In mouse, mutations of this E3 ubiquitin ligase gene can lead to infertility in adult males and females, and a deletion of this gene can cause embryonic lethality in some genetic backgrounds. A pseudogene of this gene has been identified on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013] |
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