CSB (ERCC6) (NM_000124) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC219020L1V

  • LentiORF®

Lenti ORF particles, ERCC6 (Myc-DDK tagged) - Human excision repair cross-complementing rodent repair deficiency, complementation group 6 (ERCC6), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 2,465.00

2 Weeks*

Size
    • 200 ul

Product Images

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Rabbit polyclonal antibody to CSB (excision repair cross-complementing rodent repair deficiency, complementation group 6)
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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol CSB
Synonyms ARMD5; CKN2; COFS; COFS1; CSB; CSB-PGBD3; POF11; RAD26; UVSS1
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_000124
ORF Size 4479 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC219020).
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_000124.1
RefSeq Size 8993 bp
RefSeq ORF 4482 bp
Locus ID 2074
UniProt ID Q03468
Cytogenetics 10q11.23
Domains SNF2_N, DEAD, helicase_C
Protein Families Druggable Genome
Protein Pathways Nucleotide excision repair
MW 168.3 kDa
Gene Summary This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The encoded protein has ATP-stimulated ATPase activity, interacts with several transcription and excision repair proteins, and may promote complex formation at DNA repair sites. Mutations in this gene are associated with Cockayne syndrome type B and cerebrooculofacioskeletal syndrome 1. Alternative splicing occurs between a splice site from exon 5 of this gene to the 3' splice site upstream of the open reading frame (ORF) of the adjacent gene, piggyback-derived-3 (GeneID:267004), which activates the alternative polyadenylation site downstream of the piggyback-derived-3 ORF. The resulting transcripts encode a fusion protein that shares sequence with the product of each individual gene. [provided by RefSeq, Mar 2016]

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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.