ERCC8 (NM_000082) Human 3' UTR Clone
CAT#: SC209828
3' UTR clone of excision repair cross-complementing rodent repair deficiency complementation group 8 (ERCC8) transcript variant 1 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | ERCC8 (NM_000082) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CKN1; CSA; UVSS2 |
ACCN | NM_000082 |
Insert Size | 2000 bp |
Sequence Data |
>SC209828 3’UTR clone of NM_000082
The sequence shown below is from the reference sequence of NM_000082. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCCTGGAGCAGCAGTGATGAAGAAGGATGAATATCATCTTTAGTACCTTTTTGTCTCTGCTGAAACTTT TTAAATGAGACTGTGTTTTTTTCAACTGTATGGTCTATTCCTGACAGCTAAATTAGCCCTAAATGTGGG TAATATTTTTCCTCATGTTTTAAAATGAGGTTAATATTTGCATAAAATCCTAAAACAGACTTCTGTATA GTTTATTTAGTCAAAATGTGTTCCTTGATCCCAGATGTTGTGGCCTGGGAAAGCCCTCATTGCTACAGT ACAAGTAACACAAGTCGTTGTACCTCAGTTGTGACCTTCAGCAGATTTTATGAACTATAAGATGCAGTC TCAGAGGATCAGCAAGTGGAGGCCATCAGTATTGACTTTCTCTTACTTGCTGTACTATCAGCCTGCTCG TTTCCACCTTTAAGAATGATTTTGCCAAGAATGATTATATCAAAAATAGTAGTTGAAATGGTAACATCA AAATTATTTTATTCTTTCTTCTTCATGTATTCACATTTTTCAGTGGTTTCATTTAATTAACCATGCTTT ATGTTAAACATTTTGGGGCTCAATGTCTCCTACTATCCAAAATGTGCATCACAGGAGGCTTTTAACTTT GTGAAAATCCCATGTTTGCTTTATTTTATTTTAATGTCAGAAGGCAGTTTGCGCTAATGCTTGAACTCT TTTTCTGTGAAACTCATTAAGGTATGACCAAATCCTGCCTCATTAATTCAAGCAGAAAATATCCTGGCA GGGAATCTGGCTTAAACATGAAATGCTGTAATAAAATTTCTATGTTATTGTCTCCGTCTGTGTCAACCC ACACGTGATTATCATGAAGGTAATCTTAATTTTCCCTTCCTGATCCTTACCAGCAGTAGACTAGTAAAT GAGGCTTTTATGAGCTTGAATACCAAAAGTAAACAGTTGTTGAGGGTTTTTTGTTTTTTTGTTTTTTTC CTGAGATGGAGTTTCACTCTGTCGCTCAGGCCGGAGTGCAGTGTTTTGATCTCAGCTCACTGCAACCTT CACCTCCCAGGTTCAAGCAATTCTCCTGCCTAAGCCTCCTGAGTAGCTGGGATTACAGGCTCCCGCCAC TGCGCCCGGTTAATTTTTTTGTATTTTCAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTTGCG AACTGCTGACCTCAAATGATCCACCCGCCTCGGCCTCTCAAAGTGCTGGAATTATAAGCTTGAGCCACT GCACCCAGCCAGTTGTTGAGTTTTTAAGTGTATAAGGGTTAGACCTCCTATCAGACCTTTCCAGCTAAA TGTTTTCCAAACACTTGCTTTTACAATTGATTTTTTTTTCCAATTGGCAGATAAAATTGTATGTATTTA CCATGTACAACATACTGTTTTGAAGCATATATACATTATAGAATGACTAAATCTAGCTAACTGACATAT GCCTCACATGGTTACCATTTTGTGGTAAGAACACTTTACATCCATTCTCTTATTTTTCAAAATTAATAG TAATCTTGTAATTGTAACTATAGTTACTATGTTGTGCAATAGGTCTCTTGCACTAATTCCCCCTTTTTA ACTGAAATTTTGTATCCTTTGACCAATGTTTCTCCAACAACCCTAGCTCCTGGTAACCACCATTCTACT CTCTACTTCTATGAGATCAGCTGTTTGTGTATATGTACTACATTTTCTTTATCCATTCAACCATTGACA GATGCTTAGGTTGATACCATATCCTGGCTATTGTGAATAATGCTGCAGTGAACCTGGTAGTGCAGATAT CTCTTTGACATACTGATTTCATATCCTTTGGATATAAGCCCAGTATTAGGATTGCTGGATCATATGTAG TTCTATTTTTAACTTTTTGCAGAAACTCCATACTGTCTTCCATAATGGCTGTACTAATTTACATTCCTA CCAAGAATATGCAAGAATTCCTTTTTCTTCACAATAATGCAAGAAATCCTTTTTCTTCACATCCTTGC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_000082.4 |
Synonyms | CKN1; CSA; UVSS2 |
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] |
Locus ID | 1161 |
MW | 76.4 |
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