XPB (ERCC3) (NM_000122) Human 3' UTR Clone
CAT#: SC204025
3' UTR clone of excision repair cross-complementing rodent repair deficiency complementation group 3 (xeroderma pigmentosum group B complementing) (ERCC3) 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 | XPB (ERCC3) (NM_000122) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | BTF2; GTF2H; RAD25; Ssl2; TFIIH; TTD2; XPB |
ACCN | NM_000122 |
Insert Size | 336 bp |
Sequence Data |
>SC204025 3’UTR clone of NM_000122
The sequence shown below is from the reference sequence of NM_000122. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CACCCGCTCTTCAAGCGCTTTAGGAAATGATGCTTAGGCAGGGTACTTCGTTCAAGACCGGCGCTTGGC ACCCTTGTTGGAAAGGGATTTTCAGCATAACATTTTCCTTCCACCTCTTTGACCTTCCCTCCAGCGTTG GCCAAATTGTGCTGAGGAAGATGCATCAAGGGCTTGGCTGTGCCTTCATAGGTCATCTAGGGTTTTATA AAGGAGGAGGAGACAATATTTTTTCAAACTTTTTGGGGAGTGGGGTCATTTCTGTATATAAAAAATGTT AATATTTAAGGTGTATTTATGTTACCGTTCTGAATAAACAGAATGGACCATTGAACCAGT 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_000122.2 |
Synonyms | BTF2; GTF2H; RAD25; Ssl2; TFIIH; TTD2; XPB |
Summary | This gene encodes an ATP-dependent DNA helicase that functions in nucleotide excision repair. The encoded protein is a subunit of basal transcription factor 2 (TFIIH) and, therefore, also functions in class II transcription. Mutations in this gene are associated with Xeroderma pigmentosum B, Cockayne's syndrome, and trichothiodystrophy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
Locus ID | 2071 |
MW | 12.6 |
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