ISCU (NM_213595) Human 3' UTR Clone
CAT#: SC206548
3' UTR clone of iron-sulfur cluster scaffold homolog (E. coli) (ISCU) nuclear gene encoding mitochondrial protein transcript variant 2 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 | ISCU (NM_213595) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | 2310020H20Rik; HML; hnifU; ISU2; NIFU; NIFUN |
ACCN | NM_213595 |
Insert Size | 482 bp |
Sequence Data |
>SC206548 3’UTR clone of NM_213595
The sequence shown below is from the reference sequence of NM_213595. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCCAAAAAAGGAGAGGCAGAGAAGAAATGAGCCCTCCCTCGGCGAAGCCTCCAGCAGGCCACACCAGCT GTTTCCCACCTGCTGTGCAGTCACCTTAGATGTTCAGAAGCCGCTTCCTCTCCACTGAAGAGCTATGAG ATACGCACAATACTTGCTGTTCACGTTATGACTCTCATGCAAGCAAAATACACAGTTTCATTGTTCTGA ATCCTGTGGTTTCTTTCAGCCCACTTTTATCGCCTTAACCTAGTTAATGTATATTTTGAATTGTGTGTA TGACCTCAGAACTGAAATTGATAATGAAGTTGCAAGTTTTGATAGCCCGTGAAGTGCATAAGTATCTAA TTTTACCTGAATTGATTTGGGGGGAAATTACCAGTAGAATGCCTTGGTCTGAATATTTGATAGAACCAA TTGTTGTACATAAAACAGATTGCGCATATATATATATGTATAAAAAATAATAAAATAATGGAAGATGA 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_213595.4 |
Synonyms | 2310020H20Rik; HML; hnifU; ISU2; NIFU; NIFUN |
Summary | This gene encodes a component of the iron-sulfur (Fe-S) cluster scaffold. Fe-S clusters are cofactors that play a role in the function of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, and oxidative stress response. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol or to the mitochondrion. Mutations in this gene have been found in patients with hereditary myopathy with lactic acidosis. A disease-associated mutation in an intron may activate a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein. A pseudogene of this gene is present on chromosome 1. [provided by RefSeq, Feb 2016] |
Locus ID | 23479 |
MW | 18.4 |
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