XPA (NM_000380) Human 3' UTR Clone

Specifications

Product Data
Product Name	XPA (NM_000380) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	XP1; XPAC
ACCN	NM_000380
Insert Size	560 bp
Sequence Data	Insert Sequence (showhide) >SC207401 3’UTR clone of NM_000380 The sequence shown below is from the reference sequence of NM_000380. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGCCATGAACTGACATATGAAAAAATGTGATTTTTTAGTTCAGTGACCTGTTTTATAGAATTTTATATT TAAATAAAGGAAATTTAGATTGGTCCTTTTCAAAATTCAAAAAAAAAAGCAACATCTTCATAGATGAAT GAAACCCTTGTATAAGTAATACTTCAGTAATAATTATGTATGTTATGGCTTAAAAGCAAGTTTCAGTGA AGGTCACCTGGCCTGGTTGTGTGCACAATGTCATGTCTGTGATTGCCTTCTTACAACAGAGATGGGAGC TGAGTGCTAGAGTAGGTGCAGAAGTGGTAGGTCAGCTACAAATTTGAGGACAAGATACCAAGGCAAACC CTAGATTGGGGTAGAGGGAAAAGGGTTCAACAAAGGCTGAACTGGATTCTTAACCAAGAAACAAATAAT AGCAATGGTGGTGCACCACTGTACCCCAGGTTCTAGTCATGTGTTTTTTAGGACGATTTCTGTCTCCAC GATGGTGGAAACAGTGGGGAACTACTGCTGGAAAAAGCCCTAATAGCAGAAATAAACATTGAGTTGTAC GAGTCTGA 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_000380.4
Synonyms	XP1; XPAC
Summary	This gene encodes a zinc finger protein plays a central role in nucleotide excision repair (NER), a specialized type of DNA repair. NER is responsible for repair of UV radiation-induced photoproducts and DNA adducts induced by chemical carcinogens and chemotherapeutic drugs. The encoded protein interacts with DNA and several NER proteins, acting as a scaffold to assemble the NER incision complex at sites of DNA damage. Mutations in this gene cause Xeroderma pigmentosum complementation group A (XP-A), an autosomal recessive skin disorder featuring hypersensitivity to sunlight and increased risk for skin cancer. [provided by RefSeq, Aug 2017]
Locus ID	7507
MW	21.5

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