DNA Ligase IV (LIG4) (NM_206937) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC220071L3V

  • LentiORF®

Lenti ORF particles, LIG4 (Myc-DDK tagged) - Human ligase IV, DNA, ATP-dependent (LIG4), transcript variant 2, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK w/ Puro mGFP w/ Puro


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USD 1,384.00

7 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol DNA Ligase IV
Synonyms LIG4S
Mammalian Cell Selection Puromycin
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_206937
ORF Size 2733 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC220071).
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_206937.1
RefSeq Size 3994 bp
RefSeq ORF 2736 bp
Locus ID 3981
UniProt ID P49917
Cytogenetics 13q33.3
Protein Families Druggable Genome
Protein Pathways Non-homologous end-joining
MW 104 kDa
Gene Summary The protein encoded by this gene is a DNA ligase that joins single-strand breaks in a double-stranded polydeoxynucleotide in an ATP-dependent reaction. This protein is essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ). This protein forms a complex with the X-ray repair cross complementing protein 4 (XRCC4), and further interacts with the DNA-dependent protein kinase (DNA-PK). Both XRCC4 and DNA-PK are known to be required for NHEJ. The crystal structure of the complex formed by this protein and XRCC4 has been resolved. Defects in this gene are the cause of LIG4 syndrome. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]

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