FANCL (NM_018062) Human 3' UTR Clone
CAT#: SC207278
3`UTR clone of Fanconi anemia complementation group L (FANCL) transcript variant 2 for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | FANCL |
Synonyms | FAAP43; PHF9; POG |
ACCN | NM_018062 |
Insert Size | 518 |
Sequence Data |
>SC207278 3'UTR clone of NM_018062
The sequence shown below is from the reference sequence of NM_018062. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC ATGTCTGGAAGGAAACACTGAAATAAGAATACAACATTTCGGTGAAGAGCTGGAAACTTAAAAAATTATC AAAAGGAATTTTGGTATCATCTTCAGAGAAAAAATAAAGCAAGAAATACTAACATCAAAAGGACAGGTAT GATGATGCGATAATAATAAACATCTGCGTTTGTCTCTTCACTAAGAGTAAACTGGGAAATTGTAGGCCAA AGTCCAGTTGAACTTTCTAAGTCTGTGATCCCCGTGCTGACTGTGGAAGTGTATTTATACCAAGATGGAG ATCTTGACTTCTTGAATATATCTGGACTGGTAAAATCTTGATGAGGCTCATAAAATGAGTTTGGGAATTG TGTATAGCTGATTTTTTGTGGGAAACTGTTTACTTCATTCAAAGGTTCTTGAGACTCTTGATATTTCTGT CTTCTCCTTGTGCTTTCCTATGGAAAAAATACATATATAGTTTAGTTTGTTAGACGTGAGTTATCCAAGT ATTTATTTTGTGTAGTGTGTAAGAATGC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_018062.3 |
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] |
Locus ID | 55120 |
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