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Home TrueClone ERCC8 Clone

ERCC8 (BC009793) Human cDNA Clone

Specifications Citations Clones of Other Species Product Documents
SKU Description Price Availibility*  
SC123696 ERCC8 (untagged)-Human excision repair cross-complementing rodent repair deficiency, complementation group 8, transcript variant 3 (cDNA clone MGC:13580 IMAGE:3683434), complete cds (10ug), BC009793.1, 10ug $185 3 weeks
TF81001 TurboFectin, High performance Transfection reagent (1ml/vial) $420 In Stock
TA308479 Rabbit polyclonal antibody to CSA (excision repair cross-complementing rodent repair deficiency, complementation group 8), 100ul $325 3-7 Days
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OriGene Data
Vector:pCMV6-XL5 Insert Size: 916 Restriction Site:
Sequence Data: Fully Sequenced ORF          5' Read Nucleotide Sequence         
OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Protein Families: Transcription FactorsDruggable Genome
Protein Pathways: Nucleotide excision repairUbiquitin mediated proteolysis
Reference Data
RefSeq: BC009793.1, AAH09793
RefSeq Size: 916 RefSeq ORF: 618
Synonyms : CSA;CKN1; Cockayne syndrome WD-repeat protein CSA; DNA excision repair protein ERCC-8; excision repair cross-complementing rodent repair deficiency, complementation group 8
LocusID: 1161 Cytogenetic: 5q12.1
Summary: This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014].


* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping

 

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