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


Reconstitution Protocol

USD 683.00

4 Weeks*

Size
    • 10 ug

Product Images

Frequently bought together (2)
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DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

USD 160.00

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Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol ERCC2
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).
Product Components The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials.
Reference Data
RefSeq NM_000400.4
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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