XPD (ERCC2) (NM_000400) Human 3' UTR Clone
CAT#: SC202874
3' UTR clone of excision repair cross-complementing rodent repair deficiency complementation group 2 (ERCC2) 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 | XPD (ERCC2) (NM_000400) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | COFS2; EM9; TFIIH; TTD; TTD1; XPD |
ACCN | NM_000400 |
Insert Size | 1822 bp |
Sequence Data |
>SC202874 3’UTR clone of NM_000400
The sequence shown below is from the reference sequence of NM_000400. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGGATAGAGCAGATTGCTCAGCAGCTCTGAGTGGGGCGGGTGGGGCCATAAACGGTTCCTGGTGACTCC TGAGTCTTGCCTGGCCCTGGTTCCCAGCGGCGGTGGTGCTAGAAGGTCTTATGAAGTCAGGTGACATTT CTCACTGTCACGTCCACAGCCTTTAATCGCAGGAGAAGGCAGCTATCCACCAGGTACCCAGAGGCAAGG GGGGGCCAGGAGATGATAGACCCCCTCTCACCCCACCAGCCCATCCCTCCTGCACTGTTCCCAAGAAGC TGCGGCCAGCGCAGTTCACTGGACGTTAGTGGGGGCTCAGGTCCTGGGTGCTGGCGCTGAGGGTCCGAG GGGCCTTGTCCAGGTGCCAGCTGGGAAACTGGAGACAGGCACAGGGGATGGTTGGAGGGGAGGTGAGGG GCAAGTGTTACATCCACCCTCCAGCTCCAGGTCCAGCCTGGCAGCCAACTATCCAACCCCCTCGCCTCT ACCCCAAGTAAAACCCATCTTTGCTCCTGTCCTGGGTCTCTTCTGACACCAACCCACCACCTGCTGACT CCACCACTGGCCCGACCGCCCTGCCTTTGCCTCATCTCTGCACCTACCCACATGGCCTCCTCTATTTTT GACCCAGATGTCCCCCTCACCTGAGTCCCAGGAGCCCTTGGAGCATCCACGTTCAGTGTGTTGAGTGAC ATGGCTCTCTTCATTCTGCAAAGAGGGCAGCAGGGAGGAAATGAGTGAATCCAGGAGTGGCCCCCCTCC ACGAGGGACCTTTCCAGCACAGGGTTTGATCTGTGTGTATCACAGGGGAGATGGGAGCCATGGAAGGTT CTTGAGCAAGATGGGGGTGGGGGTGGGGTGGGCTGTGGATTCTGCTGATGTCAGGGCTCTTTGCCGACC TGATCAACACTCACCCGGCTGCTCCTGCCGCCGCCTCGCCTCGGAGCCGGGAGACCAGCTTCTCACTTC CTCGCCTGATAGACTCACGGATCTTGGAGAGTGAGCTGCTGCGGCGAAGGGCCTGGGGAGGGGCCGGGG ATGCTGCTCAGTCCCCCAGGCCCATGCAGTCCCCACGCCCACCCCAGGAGCCGAAGCACAGCCCATCCT CACCTGTTCTGCGTCACCAGCTGTGCCTGTGTTGGGGGCACCTAGGGGGAAAGATGGGGGACACTGAGA TGGGGACATAGAGAAGCCACCAGGAGGGAAGACAGACAGGGGCTAGGGGCTCACCGAGAGGGGCGGGTA GGTCCTCCTTGTGGAGGATTTCTTTGTACAGCTCTTCCGCTTGTTGATACTTGTTCTGTTTCAGGTAGG CTGAGGCCTGCGGAGAAGGGAGTGTCTGGGAACTTTTCGGACCCCAGTTCCCAACACTGCATCCAGTCC CGCCTTTTTTTTTTTTTTTGTAGAGACAGGGGTCTTGGTATGTTGCCCAGGCTGGTCTTGAACTCCTAG CCTCAAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGTTGGGGTTACAAGCGTGAACCACCACGTCTGGC CCCACTTTCTAATGTGCTGACCTGGCCGTATCCTTCCCCTGCCTAAAGCCTTGCCCTGGGGCAGAGTGG GTTTGGAGCTCGGCCTTACTTCCTGCCCTGGGGATGGAGGACAGGCAGCCTCCTGTTTCTGAGCCTGTC TGCTGTACTTTGGGCTGGTGGCATGGCCTCGGTGCCTCAGTCTTCCCACACGCAAAGTGGAGCGACAGC TCCCACCTCATAGGGACGCTATAAGAACTAGCGATGTGGGGACCGGGCTAAGAGGGGAGCCGGCCACAG TGAGCTCAATAAATGTCTGCTGCTGCCA 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_000400.4 |
Synonyms | COFS2; EM9; TFIIH; TTD; TTD1; XPD |
Summary | The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008] |
Locus ID | 2068 |
MW | 64.8 |
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