XPC (NM_001145769) Human 3' UTR Clone

Specifications

Product Data
Product Name	XPC (NM_001145769) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	RAD4; XP3; XPCC
ACCN	NM_001145769
Insert Size	832 bp
Sequence Data	Insert Sequence (showhide) >SC210028 3’UTR clone of NM_001145769 The sequence shown below is from the reference sequence of NM_001145769. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCCCACCTGTTCCCATTTGAGCAGCTGTGAGCTGAGCGCCCACTAGAGGGGCACCCACCAGTTGCTGCT GCCCCACTACAGGCCCCACACCTGCCCTGGGCATGCCCAGCCCCTGGTGGTGGGGGCTTCTCTGCTGAG AAGGCAAACTGAGGCAGCATGCACGGAGGCGGGGTCAGGGGAGACGAGGCCAAGCTGAGGAGGTGCTGC AGGTCCCGTCTGGCTCCAGCCCTTGTCAGATTCACCCAGGGTGAAGCCTTCAAAGCTTTTTGCTACCAA AGCCCACTCACCCTTTGAGCTACAGAACACTTTGCTAGGAGATACTCTTCTGCCTCCTAGACCTGTTCT TTCCATCTTTAGAAACATCAGTTTTTGTATGGAAGCCACCGGGAGATTTCTGGATGGTGGTGCATCCGT GAATGCGCTGATCGTTTCTTCCAGTTAGAGTCTTCATCTGTCCGACAAGTTCACTCGCCTCGGTTGCGG ACCTAGGACCATTTCTCTGCAGGCCACTTACCTTCCCCTGAGTCAGGCTTACTAATGCTGCCCTCACTG CCTCTTTGCAGTAGGGGAGAGAGCAGAGAAGTACAGGTCATCTGCTGGGATCTAGTTTTCCAAGTAACA TTTTGTGGTGACAGAAGCCTAAAAAAAGCTAAAATCAGGAAAGAAAAGGAAAAATACGAATTGAAAATT AAGGAAATGTTAGTAAAATAGATGAGTGTTAAACTAGATTGTATTCATTACTAGATAAAATGTATAAAG CTCTCTGTACTAAGGAGAAATGACTTTTATAACATTTTGAGAAAATAATAAAGCATTTATCTAAAAAAA AAAA 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_001145769.1
Synonyms	RAD4; XP3; XPCC
Summary	The protein encoded by this gene is a key component of the XPC complex, which plays an important role in the early steps of global genome nucleotide excision repair (NER). The encoded protein is important for damage sensing and DNA binding, and shows a preference for single-stranded DNA. Mutations in this gene or some other NER components can result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]
Locus ID	7508
MW	31.5

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