XPD (ERCC2) (NM_001130867) Human 3' UTR Clone

Specifications

Product Data
Product Name	XPD (ERCC2) (NM_001130867) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	COFS2; EM9; TFIIH; TTD; TTD1; XPD
ACCN	NM_001130867
Insert Size	108 bp
Sequence Data	Insert Sequence (showhide) >SC200830 3’UTR clone of NM_001130867 The sequence shown below is from the reference sequence of NM_001130867. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCAGGAACCAAAAAAGATCTCATCCCTAACCCCCCAGAACTTATATTCCAGATGGGAAAACCAGTAGC AAAGATGCAGCCAAATAAACAAGGAAATAATTCCAGAAA 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_001130867.2
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	4.2

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