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
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


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

CNY 1,280.00

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
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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