ERCC8 (BC009793) Human Untagged Clone
CAT#: 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
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | ERCC8 |
Synonyms | CKN1; Cockayne syndrome WD-repeat protein CSA; CSA; DNA excision repair protein ERCC-8; excision repair cross-complementing rodent repair deficiency, complementation group 8 |
Vector | pCMV6-XL5 |
E. coli Selection | Ampicillin (100 ug/mL) |
Mammalian Cell Selection | None |
Sequence Data |
>OriGene sequence for BC009793 edited
GGGGGTCATGGCGACGTCCAGTGCTCCAGCCGGTGTGAGGACACGATATGCTGGGGTTTT TGTCCGCACGCCAAACGGGTTTGGAGGACCCTCTTCGCCTTCGGAGAGCAGAGTCAACAC GGAGAGTTTTGGGACTGGAATTAAATAAAGACAGAGATGTTGAAAGAATCCACGGCGGTG GAATTAACACCCTTGACATTGAACCTGTTGAAGGGAGATACATGTTATCAGGTGGTTCAG ATGGTGTGATTGTACTTTATGACCTTGAGAACTCCAGCAGACAATCTTATTACACATGTA AAGCAGTGTGTTCCATTGGCAGAGATCATCCTGATGTTCACAGATACAGTGTGGAGACTG TACAGTGGTATCCTCATGACACTGGCATGTTCACATCAAGCTCATTTGATAAAACTCTGA AAGTATGGGATACAAATACATTACAAACTGCAGATGTATTTAATTTTGAGGAAACAGTTT ACAGTCATCATATGTCTCCAGTCTCCACCAAGCACTGTTTGGTAGCAGTTGGTACTAGAG GACCCAAAGTACAACTTTGTGACTTGAAGTCTGGATCCTGTTCTCACATTCTACAGGGTA TTTTTATTTTATTTCAAACGGCAACTACTTTGAGTAAACGATTCAATAAAAAGAAACGTT ACTAACAGTGTATTCTTTGTAAGTGACATGACTAATGTACTTTGTGCTGGTTGTTGAGAC TCAGCAGGGAAATAAAGATCCTTCTGTGCATTATTCTTATAAAACTGAACCATTGAAAAC ACATTTATATGAACAATGATCATTGGGGAAGCTCAAACAATATGAAAAATAGTTCTAACT CAAAACCTTGTGTTATTTCTACATTAAAAAAACTAATGCAACTCAGAAAAAAAAAAAAAA AAAAAAAAAAAAAAAA >OriGene 5' read for BC009793 unedited
ATAGGCGGCCGCGNAATTCGCCATTACGGCCGGGGGTCATGGCGACGTCCAGTGCTCCAG CCGGTGTGAGGACACGATATGCTGGGGTTTTTGTCCGCACGCCAAACGGGTTTGGAGGAC CCTCTTCGCCTTCGGAGAGCAGAGTCAACACGGAGAGTTTTGGGACTGGAATTAAATAAA GACAGAGATGTTGAAAGAATCCACGGCGGTGGAATTAACACCCTTGACATTGAACCTGTT GAAGGGAGATACATGTTATCAGGTGGTTCAGATGGTGTGATTGTACTTTATGACCTTGAG AACTCCAGCAGACAATCTTATTACACATGTAAAGCAGTGTGTTCCATTGGCAGAGATCAT CCTGATGTTCACAGATACAGTGTGGAGACTGTACAGTGGTATCCTCATGACACTGGCATG TTCACATCAAGCTCATTTGATAAAACTCTGAAAGTATGGGATACAAATACATTACAAACT GCAGATGTATTTAATTTTGAGGAAACAGTTTACAGTCATCATATGTCTCCAGTCTCCACC AAGCACTGTTTGGTAGCAGTTGGTACTAGAGGACCCAAAGTACAACTTTGTGACTTGAAG TCTGGATCCTGTTCTCACATTCTACAGGGTATTTTTATTTTATTTCAAACGGCAACTACT TTGAGTAAACGATTCAATAAAAAGAAACGTTACTAACAGTGTATTCTTTGTAAGTGACAT GACTAATGTACTTTGTGCTGGTTGTTGAGACTCAGCAGGGAAATAAAGATCCTTCTGTGC ATTATTTCTTATAAACTGAACCCTTGAAAACACATTTATATGAACAATGATCATTGG |
Restriction Sites | Please inquire |
ACCN | BC009793 |
Insert Size | 916 bp |
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. |
Reconstitution | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
Reference Data | |
RefSeq | BC009793.1, AAH09793.1 |
RefSeq Size | 916 bp |
Locus ID | 1161 |
Cytogenetics | 5q12.1 |
Protein Families | Druggable Genome, Transcription Factors |
Protein Pathways | Nucleotide excision repair, Ubiquitin mediated proteolysis |
Gene 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]' |
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