MUS81 (NM_025128) Human Tagged ORF Clone Lentiviral Particle

SKU
RC203373L1V
Lenti ORF particles, MUS81 (Myc-DDK tagged) - Human MUS81 endonuclease homolog (S. cerevisiae) (MUS81), 200ul, >10^7 TU/mL
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    Expression-ready ORF plasmid in lenti backbone

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$1,063.00
3 Weeks*
Specifications
Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Target Symbol MUS81
Synonyms SLX3
Vector pLenti-C-Myc-DDK
Mammalian Cell Selection None
Sequence Data
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC203373).
ACCN NM_025128
ORF Size 1653 bp
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.
Shipping Dry Ice
Reference Data
RefSeq NM_025128.3, NP_079404.2
RefSeq Size 2406 bp
RefSeq ORF 1656 bp
Locus ID 80198
UniProt ID Q96NY9
Cytogenetics 11q13.1
Domains ERCC4
Protein Pathways Homologous recombination
MW 61.1 kDa
Summary This gene encodes a structure-specific endonuclease which belongs to the XPF/MUS81 endonuclease family and plays a critical role in the resolution of recombination intermediates during DNA repair after inter-strand cross-links, replication fork collapse, and DNA double-strand breaks. The encoded protein associates with one of two closely related essential meiotic endonuclease proteins (EME1 or EME2) to form a complex that processes DNA secondary structures. It contains an N-terminal DEAH helicase domain, an excision repair cross complementation group 4 (ERCC4) endonuclease domain, and two tandem C-terminal helix-hairpin-helix domains. Mice with a homozygous knockout of the orthologous gene have significant meiotic defects including the failure to repair a subset of DNA double strand breaks. [provided by RefSeq, Jun 2017]
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