PRODH (NM_016335) Human 3' UTR Clone
CAT#: SC205472
3' UTR clone of proline dehydrogenase (oxidase) 1 (PRODH) nuclear gene encoding mitochondrial protein 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 | PRODH (NM_016335) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | HSPOX2; PIG6; POX; PRODH1; PRODH2; TP53I6 |
ACCN | NM_016335 |
Insert Size | 424 bp |
Sequence Data |
>SC205472 3’UTR clone of NM_016335
The sequence shown below is from the reference sequence of NM_016335. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACTGGCAACCTCTTCCATCGCCCTGCCTAGCACCCGCCAGCACACCCTTAGCCTCCAGCACCCCCCGCC CCCGCCCAGGCCATCACCACAGCTGCAGCCAACCCCATCCTCACACAGATTCACCTTTTTTCACCCCAC ACTTGCAGAGCTGCTGGAGGTGAGGTCAGGTGCCTCCCAGCCCTGCCCAGAGTATGGGCACTCAGGTGT GGGCCGAACCTGATACCTGCCTGGGACAGCCACTGGAAACTTTTGGGAACTCTCCTCGAATGTGTGGGC CCAAGGCCCCCACCTCTGTGACCCCCATGTCCTTGGACCTAGAGGATTGTCCACCTTCTGCCAAGGCCA GCCCACACAGCCCGAGCCCCTTGGGGAGCAGTGGCCGGGCTGGGGAGGCCTGCCTGGTCAATAAACCAC TGTTCCTGCA 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_016335.6 |
Synonyms | HSPOX2; PIG6; POX; PRODH1; PRODH2; TP53I6 |
Summary | This gene encodes a mitochondrial protein that catalyzes the first step in proline degradation. Mutations in this gene are associated with hyperprolinemia type 1 and susceptibility to schizophrenia 4 (SCZD4). This gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes, DiGeorge and CATCH22. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010] |
Locus ID | 5625 |
MW | 15.1 |
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