XRCC4 (NM_022550) Human 3' UTR Clone
CAT#: SC207435
3' UTR clone of X-ray repair complementing defective repair in Chinese hamster cells 4 (XRCC4) transcript variant 3 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | XRCC4 (NM_022550) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | SSMED |
ACCN | NM_022550 |
Insert Size | 548 bp |
Sequence Data |
>SC207435 3’UTR clone of NM_022550
The sequence shown below is from the reference sequence of NM_022550. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCCCAGAAGACCTCTTTGATGAGATTTAACAGTCTCAAAAAATACTTTGATGTTCACTAGACTATGTT TTCTATTCATTTCTTTAAAATGAAAAAGGAGAATTTCAAGTCAGCAGCCGCTATTACCGTATCTTACAA TTTAATTACATACACAGTGAATTGAAACCATTGTGCAAAATGGATTACACATGTATACAAAGATACGAT TTGATGATGACACTGGCACATTATTCTAAACTATTCATTCAGCATGCCTATAATTACATAAATTGTATG AGACTTTTTGTTGCAAAGGACACATTTATCATATTCATTCACACATATTATATGTGATAGCTGTCCAAC ATCCTGTCTGGGAAGATTTTGAAAACAGGACAAAGAAAACATCATTTTAAAATGTCTTCAGCTTTTTTT GAATAGACGTATTCAAACATATTCTGAACATTGATGTTTGAACATTTTAATTTGTGTGATGATGTAGAA AATATAATTTTAGTTTGTACATAAACATTGTGAAAATCTGATAATAAAATTTTTGATACATTGAA 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_022550.4 |
Synonyms | SSMED |
Summary | The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternate transcript variants such as NM_022406 are unlikely to be expressed in some individuals due to a polymorphism (rs1805377) in the last splice acceptor site. [provided by RefSeq, Oct 2019] |
Locus ID | 7518 |
MW | 21.8 |
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